30-Second Chemistry - Tro, Nivaldo

30-SECOND
CHEMISTRY
THE 50 MOST ELEMENTAL CONCEPTS IN CHEMISTRY, EACH
EXPLAINED IN HALF A MINUTE
Editor
Nivaldo Tro
Contributors
Jeff C. Bryan
Stephen Contakes
Glen E. Rodgers
Ali O. Sezer
James Tour
Nivaldo Tro
John B. Vincent
Illustrations
Steve Rawlings
CONTENTS
Introduction
Atoms, Molecules & Compounds

GLOSSARY
Matter is Made of Particles
The Structure of the Atom
Inside the Atom
Where Did Atoms Come From?
The Dual Nature of the Electron
Where Electrons Are within an Atom
Periodic Patterns
Bonding Atoms Together
Profile: John Dalton
The Lewis Model for Chemical Bonding
Valence Bond & Molecular Orbital Theories
Opposites Attract
States of Matter
GLOSSARY
The Forces That Hold Matter Together
The Gaseous State
The Liquid State
The Solid State
Profile: Robert Boyle
Ceramics
Solutions
Chemical Reactions & Energetics

GLOSSARY
Chemical Equations
Combustion Reactions & Energy Sources
Neutralizing: Acids & Bases
Creating Solids: Precipitation Reactions
Using Chemistry to Generate Electricity
Reaction Rates & Chemical Kinetics
Profile: Humphry Davy
Energy & the First Law of Thermodynamics
Entropy & the Second Law of Thermodynamics
Entropy & the Third Law of Thermodynamics
Entropy & Spontaneous Processes
Inorganic Chemistry
GLOSSARY
The Uniqueness Principle
Colour
Cluster Chemistry
Transition Metal Catalysts
Profile: Mario Molina
Carbon: It’s Not Just for Pencils
Nanotechnology
Organic Chemistry
GLOSSARY
Organic Chemistry & Vitalism
Hydrocarbons
Alcohols
Aldehydes, Ketones & Esters
Carboxylic Acids & Amines
Profile: Friedrich Wöhler
Chemistry Copying Nature
Polymers
Biochemistry
GLOSSARY
Carbohydrates
Lipids
Amino Acids & Proteins
Profile: Anna Jane Harrison
The Biological Blueprint: Nucleic Acids
Biotech Drug Synthesis
Nuclear Chemistry
GLOSSARY
Radioactivity
Splitting the Atom
Nuclear Weight Loss
The Effect of Radiation on Life
Profile: Otto Hahn
Nuclear Medicine
Appendices
Resources
Notes on Contributors
Index
Acknowledgements
INTRODUCTION
Nivaldo Tro
The core idea of chemistry is that the whole can be explained by its parts. The
properties of matter can be explained by the bits that compose it. Understand the bits,
and you understand the whole. Philosophers call this idea reductionism. Reductionism
has not always been popular in the history of thought, nor is it clear that it is
universally true. But the stunning and ongoing success of chemistry in explaining the
behaviour of matter – even living matter – suggests that, at a minimum, reductionism
is a powerful and useful idea.
The ‘bits’ in chemistry are atoms, ions and molecules. Although the idea that
matter has fundamental ‘bits’ is quite old – it was first suggested more than 2,000
years ago – its broad acceptance is quite recent, and occurred only about 200 years
ago. Before that time, most thinkers thought that matter was continuous, that it had no
smallest bits. The advent of the scientific revolution in the sixteenth century led
thinkers to correlate their ideas about nature more carefully with empirical
measurements. Since empirical measurements supported the particulate model, the
continuous model was discarded.
Chemistry helps us understand that we - and all things around us - are made up of particles.
Once the particulate model was accepted in the 1800s, progress came relatively
quickly. Scientists began figuring out the structure of the basic particles that compose
matter, and by the early-to-mid twentieth century, chemists had good models that
explained how atoms bond together to form molecules, and how the structures of
atoms and molecules affect the properties of the substances they compose. In fact,
throughout chemistry, the relationship between structure and properties is a key
unifying theme.
A second unifying theme of chemistry is the progression from simple to complex.
It turns out that, in nature, when you put together simple particles in slightly different
ways, you can get vast complexity. Just as the 26 letters of our alphabet can be
combined in different ways to compose many words, and just as you can combine
those words in many ways to form an even larger number of complex ideas, so the 91
elements that compose matter can be combined to form many compounds, and those
compounds can be combined to form an even larger number of complex substances,
including all living things.
How far can chemistry go in its explanations? We still don’t really know. We know
that chemistry can explain how a gas behaves, but can it explain how a human brain
behaves? The second half of the twentieth century saw the outgrowth of chemistry
into biology with tremendous success. We now know details about the structures of
the complex molecules at the core of life, and how those structures affect many
attributes of living things. We have been able to custom-make molecules to fight
disease, and even change the hereditary molecules (DNA) in living organisms to alter
the characteristics of those living organisms. The twenty-first century has brought new
challenges and new directions. On one frontier, scientists are using the ideas in
chemistry to try to explain even more complex phenomena, such as human
consciousness, for example. On another frontier, scientists are using chemistry to build
ever smaller structures and machines, one atom at a time. Someday we may have
molecular submarines, capable of navigating the bloodstream to fight invading cancer
cells or viruses. On yet another frontier, scientists have created new materials such as
graphene, a two-dimensional substance only one atom thick and stronger than steel. It
seems that, at least for the foreseeable future, the power of the particulate model of
matter to explain behaviour and produce new technology will continue.
Graphene is a new, carbon-based material that is just one atom thick but is stronger than steel.
A tour of this book

In this book, we present the 50 most important ideas in chemistry. Each entry is
broken up into several parts: the 30-second chemistry is the body of the explanation;
the 3-second nucleus is the idea expressed in a single sentence; the 3-minute valence
describes how the idea fits within a wider context, or can be applied to different
circumstances. The book starts with atoms, their structures and their properties. It then
goes on to show how atoms bond together to form compounds, and how we can
understand bonding and the resulting molecules. From there we move on to the states
of matter (gases, liquids and solids) and then on to chemical reactions. We then
examine the energetics and describe the laws that govern the flow of energy. Finally,
we survey four subfields of chemistry: inorganic chemistry, organic chemistry,
biochemistry and nuclear chemistry. Our goal throughout is not to provide exhaustive
or detailed accounts of chemistry, but rather to give you a flavour of the field – to
show that behind all that happens around you and inside you, particles are doing a
complex and beautiful dance that makes it all possible.
The position of electrons within an atom is central to understanding how atoms bond together.
ATOMS, MOLECULES & COMPOUNDS
ATOMS, MOLECULES & COMPOUNDS
GLOSSARY
alkali metals The column of metals (group IA) on the far left of the periodic table that
includes lithium, sodium, potassium, rubidium, cesium and francium.
atomic number The unique number assigned to each element that corresponds to the
number of protons in the element’s nucleus.
atomic theory The idea that all matter is composed of tiny particles called atoms.
classical physics Physics before the advent of quantum mechanics.
covalent bonding The joining of atoms by the sharing of one or more electrons.
electron A subatomic particle with a negative charge and a mass of 0.00055 amu (atomic
mass unit).
element A fundamental substance that cannot be divided into simpler substances. There are
91 naturally occurring elements.
Heisenberg’s Uncertainty Principle The quantum mechanical principle that certain

quantities, such as position and momentum, cannot be simultaneously specified to arbitrary
accuracy.
ionic bonding The joining of two atoms by the transfer of an electron from one to the
other.
ionic compound A compound, usually composed of a metal and one or more non-metals,
that contains atoms joined by ionic bonds.
isotope An atom that has the same number of protons as another atom, but a different
number of neutrons.
mass number The sum of the number of protons and neutrons of an atom.
molecular compound A compound, usually composed of two or more non-metals, that

contains atoms joined by covalent bonds.
neutron A subatomic particle with no charge and a mass of 1 amu.
noble gases The column of gases (group 8A) on the far right of the periodic table that
includes helium, neon, argon, krypton, xenon and radon.
nuclear fusion The joining of two lighter nuclei to form a heavier one.
nuclear model A model for the atom in which most of the mass of the atom is contained in
a small dense nucleus composed of protons and neutrons. Most of the volume of the atom
is occupied by the electron cloud.
nucleosynthesis The process by which elements form within stars.
proton A subatomic particle with a positive charge and a mass of 1 amu.
quantum mechanics The realm of physics, developed in the early twentieth century, that
deals with the very smallest particles that exist.
Schrödinger’s Cat thought experiment A thought experiment involving the application

of the uncertainty principle to a cat in a box with a radioactive substance that has a 50 per
cent chance of decaying. If the atom decays, then the cat dies, so the cat is in a strange state
of being both dead and undead, with a 50 per cent probability of each. Schrödinger used
this experiment to show that quantum mechanical ideas are not applicable to large scale
objects (such as cats).
valence electrons The highest energy electrons (and therefore the most important in
bonding) in an atom.
velocity A measure of how fast (and in what direction) an object is moving.

MATTER IS MADE OF PARTICLES
the 30-second chemistry
The Ancient Greek philosophers believed that matter was infinitely divisible – that matter
had no fundamental particles. Subsequent thinkers followed suit for more than 2,000 years.
It was not until the eighteenth and nineteenth centuries that early chemists used careful
measurements – primarily the relative weights of related samples of matter – to determine
otherwise. And it wasn’t until the early twentieth century that the question was definitely
settled: the 1926 Nobel Prize for Physics was awarded to Jean Perrin for settling the matter.
The Greeks were wrong – matter is particulate (it is made up of particles), and those
particles are called atoms. And that turns out to be among the most important ideas in all of
human thought. Why? Because the idea that matter is made of particles has enabled us to
understand nature from the bottom up. What we found was remarkable: as far as we can
tell, the particles that compose matter – their composition and structure – determine the
properties of matter. Matter does what the particles that compose it do. Water boils at
100°C (212°F) because the three atoms that compose a water molecule bond together in a
certain order, at a certain angle and at certain distances. Change any of these characteristics
and water would be a different substance.
3-SECOND NUCLEUS
Matter is composed of particles. The nature of the particles – especially their structure – determines the
properties of matter.
3-MINUTE VALENCE
Humans have wondered about the fundamental composition of matter for 2,500 years. The basic
question is this: if you divide a sample of matter into smaller and smaller pieces, could you go on forever
or would you eventually get to fundamental particles that are no longer divisible? For most of civilization,
humans got the answer to this question wrong.
RELATED TOPICS
See also
THE STRUCTURE OF THE ATOM
INSIDE THE ATOM
WHERE DID ATOMS COME FROM?
3-SECOND BIOGRAPHIES
JOHN DALTON
1766–1844
English chemist who articulated the atomic theory of matter
JEAN PERRIN
1870–1942
French physicist who studied the motion of tiny particles suspended in liquid to experimentally settle the
question of the particulate nature of matter
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Jean Perrin won the Nobel Prize essentially for proving the existence of atoms.
In 1897, J. J. Thomson discovered a new type of particle – the electron – that was much
smaller than the atom itself. Thomson demonstrated that electrons were negatively charged,
that they were present in all different kinds of matter and that their mass was 1/2,000th the
mass of the lightest atom. Thomson’s discovery implied that the atom itself was composed
of even smaller particles. Based on his discovery, Thomson developed a model for the
atom called the ‘plum-pudding model’. In this model, even the lightest atoms were
composed of thousands of electrons held in a sphere of positive charge. In 1909, Ernest
Rutherford (pictured) set out to confirm Thomson’s model, but he proved it wrong instead.
Rutherford accelerated particles (8,000 times more massive than electrons) at a thin sheet
of gold atoms. Most of these particles were not deflected by the gold atoms, but a few
bounced back. Rutherford claimed that his results were ‘about as credible as if you fired a
15-inch [38-cm] shell at a piece of tissue paper and it came back and hit you.’ Rutherford
developed a new model for the atom – the nuclear model – in which the mass of the atom is
concentrated in a small space called the nucleus. Most of the volume of the atom is empty
space.
3-SECOND NUCLEUS
An atom consists of a tiny nucleus – containing protons and neutrons – with electrons in a diffuse cloud
surrounding the nucleus.
3-MINUTE VALENCE
Matter is particulate – it is made of particles. But what are those particles like? What is their structure? The
earliest models implied that the distribution of matter within an atom was fairly uniform, but later
experiments suggested otherwise. The atom itself is mostly empty space with nearly all of the mass
contained in a small space called the nucleus.
RELATED TOPICS
See also
INSIDE THE ATOM
THE DUAL NATURE OF THE ELECTRON
J. J. THOMSON
1856–1940
English physicist who discovered the electron
ERNEST RUTHERFORD
1871–1937
New Zealand physicist whose famous Gold Foil Experiment established the nuclear model for the atom
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The nuclear atom, with the nucleus enlarged to be visible. If drawn to scale,
the nucleus would be a tiny dot, too small to see.
INSIDE THE ATOM
The number of protons in the nucleus of an atom is called the atomic number (Z) and it
determines the identity of the atom and its corresponding element. For example, helium
(Z=2) has two protons in its nucleus and sodium (Z=11) has eleven protons in its nucleus.
The number of known elements ranges from Z=1 to Z=118 – as shown in the periodic table
on the facing page. Each element has a name, a symbol and a unique atomic number. The
number of neutrons in the nucleus of an atom can vary within atoms of the same element.
For example, most helium atoms have two neutrons, but some have three. Atoms with the
same number of protons but a different number of neutrons are called isotopes. Since most
of the mass of an atom is due to its protons and neutrons, the sum of the numbers of these
two particles is called the mass number (A). Scientists specify isotopes with the following
notation: , where X is the chemical symbol, Z is the atomic number and A is the mass
number. For example, the helium isotope with 2 neutrons is specified by .
3-SECOND NUCLEUS
An atom is composed of protons, neutrons and electrons. The number of electrons in a neutral atom
always equals the number of protons in its nucleus.
3-MINUTE VALENCE
All atoms are composed of the same three subatomic particles: protons, neutrons and electrons (see table
below). So what makes one atom different from another? The numbers of those particles. Incredible as it
may seem, both sodium (a reactive metal that explodes in water) and helium (an inert gas that reacts with
nothing) are made of the same subatomic particles, just different numbers of them.
RELATED TOPICS
See also
PERIODIC PATTERNS
RADIOACTIVITY
3-SECOND BIOGRAPHY
JAMES CHADWICK
1891–1974
English physicist who discovered the neutron
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Subatomic Particles
Mass (amu) Charge (relative)
Proton 1.0 +1
Neutron 1.0 0
Electron 0.00055 -1
The periodic table lists the 118 known elements (91 naturally occurring and 27
synthetic) according to their atomic number (top left in each element box).
According to the big bang model, our universe began as a hot, dense collection of matter
and energy that rapidly expanded and cooled. During the first 20 minutes of that expansion,
hydrogen and helium (the two most abundant elements in the universe) formed from the
soup of subatomic particles. Then nucleosynthesis stopped as the universe continued to
expand and cool. Eventually, after about 500 million years, the first stars formed. Stars are
the nurseries in which all other elements are made. As stars burn – through a process called
nuclear fusion – they fuse together the nuclei of smaller atoms to form larger atoms. Young
stars fuse hydrogen atoms to form helium. This fusion gives off tremendous amounts of
heat and light and can power a star for billions of years. As a star ages, and if it is large
enough, fusion can continue to form larger atoms such as carbon and oxygen – all the way
up to iron. The formation of elements beyond iron requires the input of energy, and only
happens in the supernova stage of a star’s life. A supernova is essentially a large exploding
star. The energy emitted by a supernova can power the nucleosynthesis of elements up to
uranium, the heaviest naturally occurring element.
3-SECOND NUCLEUS
Atoms form through nucleosynthesis, which began in the first few minutes after the big bang and happens
to this day within the core of stars and supernovae.
3-MINUTE VALENCE
Our planet naturally contains about 91 different elements. Where did the atoms that compose these
elements come from? How did atoms form? They formed through a process called nucleosynthesis, which
began about 13.7 billion years ago at the very birth of our universe.
RELATED TOPICS
See also
RADIOACTIVITY
SPLITTING THE ATOM
NUCLEAR WEIGHT LOSS
ARTHUR EDDINGTON
1882–1944
English astronomer and physicist who first suggested that stars are powered by fusion
FRED HOYLE
1915–2001
English astronomer who formulated the theory of nucleosynthesis within stars
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In stars, smaller atoms fuse together to form larger atoms. All atoms beyond
helium were born in the core of stars and supernovae.
An electron travelling through space behaves very differently from a baseball flying
towards the outfield. A baseball has a definite trajectory – a deterministic path that it
follows. A good outfielder can predict where a baseball will land. This prediction requires
the outfielder simultaneously to know two properties of the flying baseball: its position
(where it is) and its velocity (how fast it is going). If the outfielder only knew one of these
two properties, he or she could not predict the baseball’s path. An electron behaves
differently because it has a dual nature: a wave nature (associated with its velocity) and a
particle nature (associated with its position). The key to understanding electron behaviour
is Heisenberg’s Uncertainty Principle, which states that ‘an electron never exists as both a
wave and a particle simultaneously’. It is either one or the other, but not both. Although
Heisenberg’s principle solved a great paradox (how something can be both a wave and a
particle), it implied the death of determinism. If you can’t observe the wave nature and
particle nature of the electron simultaneously, then you can’t simultaneously know its
velocity and its position, which means you can’t predict its future path.
3-SECOND NUCLEUS
For electrons and other small particles, the trajectories of classical physics are replaced with the
probability distributions of quantum mechanics.
3-MINUTE VALENCE
Are the smallest particles that exist, such as electrons, just like those that we can see with our eyes only
smaller? Does an electron orbiting an atom behave like a planet orbiting the Sun? No. Electrons behave
differently. Electrons, and other small particles, have a wave-particle duality that makes it impossible to
predict exact trajectories for them. Instead, we describe their behaviour in terms of probability.
RELATED TOPICS
See also
INSIDE THE ATOM
WHERE ELECTRONS ARE WITHIN AN ATOM
PERIODIC PATTERNS
ERWIN SCHRÖDINGER
1887–1961
Austrian physicist central to the development of quantum mechanics and known for the thought
experiment ‘Schrödinger’s Cat’
WERNER HEISENBERG
1901–76
German physicist who articulated the ‘Uncertainty Principle’
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In an atom, electrons do not orbit the nucleus like planets orbit the Sun.
Instead, they exist in clouds of probability.
The electron orbits of early atomic models were later replaced by quantum mechanical
orbitals. Unlike a planetary orbit, an orbital is a three-dimensional probability map that
shows the probability of finding an electron in a certain volume of space. You can
understand an orbital with a simple analogy. Imagine taking a photo every 10 seconds for
several minutes of a moth flying around a light bulb, and then superimposing all the photos
to make a single image. The result shows the light bulb with dozens of images of the moth.
The volume immediately surrounding the light bulb has many moth images, indicating a
high probability of finding the moth in that space. Further away from the light bulb there
are fewer moth images, meaning that the probability of finding the moth in that space is
lower. A quantum mechanical orbital is analogous – the light bulb is the atomic nucleus
and the moth is the electron. Just as the early model of the atom had many different orbits
at different distances from the nucleus and with different energies, so the quantum
mechanical model has many different orbitals, each with different average distances from
the nucleus and with different energies. Electrons can be observed in one orbital or another,
but never in between.
3-SECOND NUCLEUS
Electrons in atoms exist in quantum mechanical orbitals, three-dimensional probability maps that show
the likelihood of finding the electron in a certain volume of space.
3-MINUTE VALENCE
Atoms bond together by sharing or transferring electrons. As a result, the positions of electrons within an
atom – where they are – is important because it affects how atoms bond together. In an early model,
electrons were thought to orbit the nucleus of the atom much like planets orbit the Sun. However, this
model was later proved wrong and was replaced with the quantum mechanical model for the atom.
RELATED TOPICS
See also
BONDING ATOMS TOGETHER
NIELS BOHR
1885–1962
Danish physicist central to the development of the quantum mechanical model for atomic structure
ERWIN SCHRÖDINGER
1887–1961
Austrian physicist central to the development of the quantum mechanical model of the atom
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Early atomic models had electrons orbiting the nucleus like planets orbit the
Sun. These have been replaced by the quantum mechanical model.
PERIODIC PATTERNS
The ancient Greeks thought that matter was composed of only four elements: earth, water,
fire and air. By the mid-1800s, however, scientists had discovered more than 50 different
elements. Dmitri Mendeleev noticed a pattern in the properties of known elements when he
listed them in order of increasing atomic number: certain properties recurred periodically.
Based on this observation, Mendeleev constructed a table of elements with atomic number
increasing from left to right, and elements with similar properties aligning in columns. His
table contained some gaps that allowed him to predict the existence and properties of yet
undiscovered elements (which were later discovered). Mendeleev’s table evolved into the
modern periodic table, which lists all known elements to date. The elements on the left and
middle of the table are mostly metals, and the elements on the right side of the table are
mostly non-metals. Each column represents a family of elements with similar properties.
For example, the far left column contains the alkali metals, a family of elements that are all
solid metals at room temperature and highly reactive. The far right column, by contrast,
contains the noble gases, a family of elements that are all gases at room temperature and
display little or no chemical reactivity.
3-SECOND NUCLEUS
When elements are listed in order of increasing atomic number, their properties recur in a regular pattern.
3-MINUTE VALENCE
Our Earth contains about 91 different naturally occurring elements, each one with its own distinctive
properties. However, certain groups of elements share similarities. The periodic law and the
corresponding periodic table allow us to organize the known elements in ways that help us make sense of
their properties.
RELATED TOPICS
See also
INSIDE THE ATOM
THE UNIQUENESS PRINCIPLE
JULIUS LOTHAR MEYER
1830–95
German chemist who made significant contributions to the periodic table
DMITRI MENDELEEV
1834–1907
Russian chemistry professor who formulated the periodic law and constructed one of the first periodic
tables
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Mendeleev formulated one of the first periodic tables, which organizes

elements according to atomic number and chemical properties.
Atoms bond together by either sharing (covalent bonding) or transferring (ionic bonding)
the electrons in their highest-energy orbitals to form compounds. Sharing of electrons
typically occurs between two or more non-metals, resulting in a molecular compound, so
called because it is composed of distinct molecules (groups of atoms bonded together).
Transfer of electrons typically occurs from a metal to a non-metal and results in an ionic
compound. Ionic compounds do not contain distinct molecules, but rather exist as an array
of ions (charged particles) with alternating positive and negative charge. Water is a good
example of a molecular compound. We represent a compound with a chemical formula,
which tells us the elements present in the compound and the relative number of atoms of
each one. For example, the formula for water is H2O, which means that a water molecule is
composed of two hydrogen atoms and one oxygen atom, and the formula for sucrose (table
sugar) is C12H22O11. Molecular compounds can contain as few as two atoms in a molecule
to as many as thousands. Sodium chloride (table salt) is a good example of an ionic
compound. The formula for sodium chloride is NaCl, which indicates sodium and chlorine
in a one-to-one atomic ratio.
3-SECOND NUCLEUS
Atoms bond together to form compounds. A compound, unlike a mixture of elements, contains two or
more elements in a fixed, definite proportion.
3-MINUTE VALENCE
The universe contains 118 different elements, but would be lifeless if these elements did not bind
together to form compounds. When two or more elements combine to form a compound, a completely
new substance forms with properties much different from the elements that compose it. In this way, our
universe’s 118 different elements can form millions of compounds. And this, among other things, makes
life possible.
RELATED TOPICS
See also
THE LEWIS MODEL FOR CHEMICAL BONDING
VALENCE BOND & MOLECULAR ORBITAL THEORIES
JOSEPH PROUST
1754–1826
French chemist who made observations on the composition of compounds
LINUS PAULING
1901–94
American chemist who made significant contributions to our understanding of chemical bonding
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Water is a molecular compound, composed of two hydrogen atoms bonded to

one oxygen atom.
JOHN DALTON
John Dalton was born into a poor, staunchly

Quaker family in the town of Eaglesfield in
northern England in 1766. At the age of 10 he
was sent to a nearby Quaker School and just
two years later began teaching there.
Soon afterwards he started to teach and
study in Kendal, where he began to carry out
and record meteorological observations, many
with instruments that he built himself. He did
this for 57 years until the day he died, recording
more than 200,000 observations. He once
wrote that ‘my head is too full of triangles,
chymical processes and electrical experiments,
etc., to think much of marriage.’
Moving to Manchester as a tutor in mathematics and natural philosophy, he joined the
Manchester Literary and Philosophical Society. His first communication at the society described a
red-green ‘colour blindness’ – from which he and his brother suffered – that is still referred to as
‘daltonism’.
His love of meteorology led him to consider the composition of the air and the nature of its
component gases. He concluded that the atmosphere is a mixture of gases and that the total
pressure it exerts is the sum of the ‘partial pressures’ that each individual gas exerts. The overall
pressure, he maintained, is due to the particles (what we would call atoms and molecules) of
these gases slamming against the walls of the container in which they are held.
Most famously, Dalton devised the first concrete atomic theory that organized a number of the
assumptions known at the time, starting with the Greek idea of indivisible atoms. He maintained
that the atoms of a given element are unique (particularly in mass) and combine with atoms of
another element in whole-number ratios. In chemical reactions, atoms are reshuffled from one
configuration to another. He went on to construct one of the first ever tables of atomic weights
but this was marred by inaccuracies that could have been easily corrected had he been more
open to valuable new ideas from the international scientific community. Despite these difficulties
his theory could be tested and its general assumptions held up well.
Given that Dalton had taken a concept that had been imprecisely discussed and largely
rejected for 2,000 years and fashioned it into a guiding paradigm that revolutionized all of
science, his colleagues were anxious to honour him. However, due to his Quaker beliefs he
refused many of these honours, including a doctorate degree from Oxford University that would
have required him to wear scarlet robes. Later, told that the robes were in fact green (he was
colour-blind, after all), he received the degree. When Dalton died, he could not stop 40,000 people
filing past his coffin and 100 coaches following his funeral cortège.
Glen E. Rodgers
1766
Born in Eaglesfield, England in a white bungalow that still stands
1776
Sent to Pardshaw Hall Quaker School
1781–93
Teaches at the Stramongate School in Kendal
1787
Begins to keep meteorological diaries
1793
Now at the New College in Manchester, publishes a paper on red-green colour blindness now
often known as ‘daltonism’
1801
Formulates Dalton’s Law of Partial Pressures
1803
Delivers a paper in which he first describes his atomic theory
1808
Publishes A New System of Chemical Philosophy, in which his atomic theory is presented in full
1810
Nominated for membership of the Royal Society but refuses the offer because Quakers resist
public recognition
1822
Renominated and elected to the Royal Society without his knowledge
1826
Receives the Royal Society’s first Royal Medal
1832
Initially refuses an honorary doctorate degree from Oxford University that would have required
him to wear scarlet robes. Persuaded that the robes were a dull green, he accepts the degree
1844
Dies and is accorded a civic funeral with full honours
In the simplest model for chemical bonding, called the Lewis model, atoms share or
transfer their highest energy electrons (called valence electrons) to obtain an octet – eight
electrons in their highest energy (or outermost) set of orbitals. One important exception is
hydrogen, which shares/transfers its one electron to obtain a duet – two electrons in its
outermost orbital. When applying the Lewis model, chemists use special symbols to
represent atoms and their valence electrons. For example, the Lewis symbols for hydrogen
and oxygen are as follows:
The one dot next to H represents hydrogen’s one valence electron and the six dots around
the O represent oxygen’s six valence electrons. The bonding between hydrogen and oxygen
to form water involves the sharing of the valence electrons, and we draw the Lewis symbol
for water as follows:
The shared electrons (those between two elements) count towards the octet (or duet) of
both atoms. So in this Lewis structure, each hydrogen atom has a duet and oxygen an octet.
3-SECOND NUCLEUS
In the Lewis model for chemical bonding, atoms bond to obtain octets – eight electrons in their valence
shell.
3-MINUTE VALENCE
The most powerful pieces of scientific knowledge are theories (or models). Theories explain not only what
happens in nature but also why it happens. The Lewis model for chemical bonding explains why, for
example, water is H2O and not some other combination of atoms. The Lewis model is simple, however,
and other more sophisticated models are even more powerful at predicting and explaining chemical
bonding.
RELATED TOPICS
See also
3-SECOND BIOGRAPHY
GILBERT N. LEWIS
1875–1946
American chemist and University of California, Berkeley chemistry professor who constructed the Lewis
model for chemical bonding
30-SECOND TEXT
Nivaldo Tro
The Lewis model shows how atoms share electrons to obtain octets.
Chemists use three different models to explain chemical bonding: the Lewis model,
valence bond theory and molecular orbital theory, each increasingly complex but also
increasingly powerful. The Lewis model requires nothing more than paper and pencil to
enable chemists to predict and explain a great deal of chemical behaviour. Valence bond
and molecular orbital theory, by contrast, both require more complex calculations, usually
on a computer. In valence bond theory, a chemical bond is modelled as the overlap between
half-filled atomic orbitals. As the orbitals overlap, the energy of the electrons in those
orbitals decreases, stabilizing the molecule relative to its constituent atoms. A molecular
orbital is to a molecule what an atomic orbital is to an atom. Each molecule has its own
unique set of molecular orbitals that depend on the constituent atoms and their arrangement
in space. If the overall energy of the electrons in the molecular orbitals is lower than in the
constituent atoms’ atomic orbitals, the resulting molecule is stable. Both valence bond
theory and molecular orbital theory can accurately predict details about molecular structure
including molecular geometries, bond lengths and bond strengths.
3-SECOND NUCLEUS
In the valence bond model, a chemical bond is the overlap between half-filled atomic orbitals. In
molecular orbital theory, atomic orbitals are completely replaced by molecular orbitals.
3-MINUTE VALENCE
The Lewis model for chemical bonding is practical and useful; however, it also has limits. We know, for
example, that electrons are not stationary dots that sit between atoms. Two more powerful bonding
models – valence bond theory and molecular orbital theory – take into account the quantum mechanical
nature of electrons and provide even more powerful predictions and explanations of chemical bonding.
RELATED TOPICS
See also
JOHN EDWARD JONES
1894–1954
English mathematician, physicist and pioneer of computational chemistry
LINUS PAULING
1901–94
American chemist who made significant contributions to valence bond theory
30-SECOND TEXT
Nivaldo Tro
Molecular orbital theory predicts that oxygen should be a magnetic liquid,

which it is. The simpler bonding theories fail to predict this property.
OPPOSITES ATTRACT
We know from previous entries that atoms can bond together by sharing electrons. But if
the bonding atoms are different (two different elements), then the sharing is often not equal
– one of the two atoms hogs the electron more than the other. The result is a polar bond,
one that has a positive end on one side and a negative end on the other. In a molecule, polar
bonds may add together to result in a polar molecule. Polar molecules interact strongly
with one another because the positive end of one molecule is attracted to the negative end
of its neighbour – just as the north pole of a magnet is attracted to the south pole of another
magnet. These attractions affect the properties of the substances that the molecules
compose. For example, polar substances tend to have higher melting and boiling points
than their nonpolar counterparts because the attraction between neighbouring molecules
makes the molecules more difficult to separate. Polar substances also tend not to mix well
with nonpolar substances. For example, water and oil do not mix because water is very
polar and oil is nonpolar. Water and ethyl alcohol (ethanol), by contrast, mix in all
proportions because they are both polar.
3-SECOND NUCLEUS
The often uneven distribution of electrons that can result when two different atoms bond together results
in a polar bond, which greatly affects a substance’s properties.
3-MINUTE VALENCE
The existence of liquid water on Earth’s surface can be attributed to polar bonds. Most small molecules
are gases at room temperature, but water is among the very few that is a liquid. Why? Because water has
highly polar bonds with hydrogen at one end and oxygen on the other. The small size of hydrogen allows
the molecules to get very close together and interact strongly. This strong interaction makes it difficult to
separate water molecules from one another.
RELATED TOPICS
See also
THE FORCES THAT HOLD MATTER TOGETHER
THE LIQUID STATE
JOHANNES DIDERIK VAN DER WAALS
1837–1923
Dutch physicist who was among the first to postulate forces between molecules
LINUS PAULING
1901–94
American chemist who quantified the polarity of chemical bonds
30-SECOND TEXT
Nivaldo Tro
A polar molecule has an asymmetrical charge distribution that causes an

attraction to other polar molecules.
STATES OF MATTER
STATES OF MATTER
GLOSSARY
amorphous solid A solid whose atoms or molecules are not arranged in an ordered,
repeating, three-dimensional array.
covalent bond The joining of atoms by the sharing of one or more electrons.
crystalline solid A solid whose atoms or molecules are arranged in a well-ordered,

repeating, three-dimensional array.
dipole force The attractive force that exists between two or more polar molecules due to an
asymmetric distribution of charge.
dispersion force The attractive force that exists between atoms and molecules due to
temporary dipoles that develop because of charge fluctuations.
homogeneous mixture A mixture containing two or more components that has the same
composition throughout.
intermolecular forces Attractive forces that exist between atoms and molecules.
ionic bond The joining of two atoms by the transfer of an electron from one to the other.
‘like dissolves like’ principle The idea that polar molecules mix well with other polar
molecules, but don’t mix well with nonpolar molecules. Mostly applicable to aqueous
solutions.
macroscopic properties of gases Properties such as temperature, volume, pressure and

number of moles of a sample of a gas.
osmotic pressure The pressure required to stop osmotic flow. Osmotic flow is the flow of
water through a semipermeable membrane from a more dilute solution to a more
concentrated one.
polar bond A chemical bond with asymmetric charge distribution.
polar molecule A molecule containing polar bonds that also has an asymmetric charge
distribution over the entire molecule.
polar solute A solute (component of a solution) that has an asymmetric charge

distribution. A nonpolar solute has a highly symmetrical charge distribution.
single liquid phase A liquid mixture with uniform composition.
solute The minority component of a solution.

solvent The majority component of a solution.
vapour pressure The pressure of the vapour of a liquid in equilibrium with its liquid.
Matter exists in three states: solid, liquid and gas. In the gas state, the particles that
compose matter are separated by large distances and do not interact with one another very
much. In the solid and liquid states, by contrast, the particles interact strongly, held
together by attractive forces. Some solids, such as a diamond, are held together by covalent
chemical bonds between atoms (which is what makes diamond so strong). Other solids,
such as table salt, are held together by ionic bonds between ions. Still other solids, such as
ice, and many liquids are held together by attractive forces that exist between molecules.
These forces are known as intermolecular forces. Intermolecular forces exist because the
electron distribution in a molecule can be either temporarily asymmetrical, resulting in the
dispersion force, or permanently asymmetrical, resulting in the dipole force. In either case,
the asymmetrical electron distribution causes part of the molecule to be positively charged
(either temporarily or permanently) and another part to be negatively charged. The positive
and negative ends of neighbouring molecules are then attracted to one another much like
opposite poles of a magnet are attracted to one another. These attractions must be overcome
for a substance to melt or boil.
3-SECOND NUCLEUS
Solid and liquid matter exist because the particles that compose them have strong attractions to one
another.
3-MINUTE VALENCE
Why are some substances solid at room temperature, while others are liquids or gases? Because the
particles that compose matter are attracted to one another in varying degrees. Strong attractions
between particles are responsible for solids at room temperature, moderately strong attractions result in
liquids and weak attractions result in gases. The higher the temperature, the stronger the attractions
between particles must be to maintain the liquid and solid state.
RELATED TOPICS
See also
OPPOSITES ATTRACT
THE LIQUID STATE
THE SOLID STATE
3-SECOND BIOGRAPHY
JOHANNES DIDERIK VAN DER WAALS
1837–1923
Dutch physicist who was among the first to postulate forces between molecules
30-SECOND TEXT
Nivaldo Tro
The strength of the intermolecular forces between water molecules in ice

determines its melting point.
THE GASEOUS STATE
Gases have the unique property – unlike solids and liquids – of always completely filling
the volume of their container. By the end of the eighteenth century, the relationships
between the volume, pressure and amount of gas had been empirically described. Hot-air
balloonists Jacques Charles (of Charles’ law fame) and Joseph Gay-Lussac not only set
new altitude records for ballooning, but also used these adventures to collect data on the
temperature-volume relationship of gases, which indicated that the volume occupied by a
gas increased with temperature. Robert Boyle demonstrated that the volume occupied by a
gas is inversely proportional to its pressure, a relationship that became known as Boyle’s
law. Amedeo Avogadro hypothesized that equal volumes of gas were occupied by equal
numbers of molecules as part of his theory that gases consisted of molecules that in turn
were composed of atoms. His theory was largely ignored at the time. Further progress in
understanding the origin of these relationships required the acceptance by chemists of the
theory of the particle nature of atoms and molecules. The current model to explain these
properties is kinetic-molecular theory.
3-SECOND NUCLEUS
Kinetic-molecular theory explains the macroscopic properties of gases based on the behaviour of gas
particles.
3-MINUTE VALENCE
Kinetic-molecular theory is based on three postulates. The sizes of the particles that comprise a gas are
negligibly small, so that gas particles occupy essentially none of the volume of a gas. Gas particles are in
constant motion and have an average kinetic energy proportional to the temperature of the gas.
Collisions between gas molecules are perfectly elastic in that energy can be transferred but not lost in the
collisions.
RELATED TOPICS
See also
ENTROPY & THE SECOND LAW OF THERMODYNAMICS
3-SECOND BIOGRAPHY
JAMES CLERK MAXWELL
1831–79
Scottish mathematician who, while best known for his work in electromagnetism, also worked on
developing a statistical means of explaining the properties of gases
30-SECOND TEXT
John B. Vincent
The properties of gases make both hot-air ballooning and scuba diving
possible.
THE LIQUID STATE
The molecules that compose a liquid are like dancers in a crowded night club. The dancers
have so much energy that they move around the floor constantly interacting with different
people. They are attracted to everyone else in the club and want to dance with everyone.
Similarly, molecules in liquids have attractive forces with all the other molecules around
them, but they have so much energy that they don’t stay still and are constantly moving
past one another. As a whole, the people in the dance club have the same shape as the club.
If they all moved from a square club to a circular one, their overall shape would change.
Similarly, as a whole, water molecules flow to assume the shape of their container. Not
every molecule in a liquid (or person in a dance club) has the same amount of energy.
Some have more, some have less. A few have a lot more energy – so much that they can
break free of their attraction to the other molecules in the liquid and fly out on their own as
a gas molecule (they essentially dance right out of the club). This is how liquids evaporate.
3-SECOND NUCLEUS
Liquids are made up of molecules with enough energy to flow past one another, but generally not enough
to overcome their mutual attraction entirely.
3-MINUTE VALENCE
Pour water into a glass – it fills to a certain level, and the shape of the water is the same as the inside of
the glass. If you pour the water into a square-shaped glass, it assumes that shape. If you leave the water
to stand for a few days, it slowly evaporates away. How do we explain this behaviour from a particulate
viewpoint?
RELATED TOPICS
See also
THE GASEOUS STATE
ROGER JOSEPH BOSCOVICH
1711–87
Ragusan (now Croatia) physicist who predicted that the states of matter depended on forces between
their particles
FRANÇOIS-MARIE RAOULT
1830–1901
French chemist who explored the properties of solutions
30-SECOND TEXT
Jeff C. Bryan
The molecules that compose the liquid state are in constant motion, not unlike
dancers in a crowded night club.
THE SOLID STATE
The particles that compose a solid are like the dancers in the nightclub from the previous
entry (on liquids), except that they have less energy relative to the strength of their
attractions. The dancers are still shaking, but they are not moving around each other
because they are strongly attracted to those currently surrounding them. Similarly, the
attractions between the particles in a solid are so strong compared to the energy they
possess that the particles don’t flow past one another as they do in a liquid. The particles
that compose a crystalline solid are not only stuck in one place, but also arranged in an
orderly fashion like bricks in a wall. In contrast, the particles that compose an amorphous
solid are arranged in a more haphazard way, like a pile of macaroni. Crystalline solids
(such as salt or ice) tend to be less flexible than amorphous solids (such as plastic or glass).
Although the particles that compose solids do not move past or around one another, they do
wiggle and shake. When heated, they get more energy. Eventually, when heated enough,
they start moving past one another and the solid melts. The amount of energy (temperature)
needed for melting depends on how strongly the molecules are attracted to each other.
3-SECOND NUCLEUS
Solids have a definite size and shape because the particles that compose them are stuck in place.
3-MINUTE VALENCE
Solids behave differently from liquids or gases. They have a fixed shape and size and don’t assume the
shape of their container like a liquid, nor are they compressible like a gas.
RELATED TOPICS
See also
THE LIQUID STATE
WILLIAM LAWRENCE BRAGG
1890–1971
Australian-born British physicist and winner of the 1915 Nobel Prize in Physics who discovered how to
peer in at the structures of solids
LINUS PAULING
1901–94
American winner of the 1954 Nobel Prize in Chemistry, who developed our understanding of how atoms
and molecules are attracted to each other
30-SECOND TEXT
Jeff C. Bryan
The molecules in the solid state are like dancers who are stuck in one place on
the dance floor.
ROBERT BOYLE
Robert Boyle, born in a castle in Lismore,

Ireland in 1627, was the 14th child of Richard
Boyle, the Great Earl of Cork and one of the
richest men in Britain. Boyle’s father sent his
12-year-old son on a Grand Tour of Paris,
Geneva and Florence that kept him safe during
the Irish Rebellion of 1641. In Geneva, during a
fearsome, life-threatening thunderstorm, he
pledged to devote his life to promoting God’s
work on Earth. His ensuing religiosity
continued for the rest of his life.
He returned to London to live with his sister
Katherine (the ‘Lady Ranelagh’) in 1644 and
together they became early members of the
‘Invisible College’, so named because it did not
have a regular meeting place, which met to
discuss science – then still known as ‘natural philosophy’. In Stalbridge, Dorsetshire, convinced
that observations and experiments were the cornerstones on which scientific investigations had
to be built, he set up his first laboratory.
Boyle is properly regarded as a transitional figure between alchemy and chemistry. He was
responsible for dropping the ‘al-’ of alchemy and is best referred to as a ‘chymist’. Among many
other interests, he was devoted to chrysopoeia, the science of transmutating ‘base metals’ into
gold. Starting in 1654, he and his assistant Robert Hooke set up a laboratory in Lady Ranelagh’s
house in Oxford. Hooke built a ‘pneumatic engine’ or vacuum pump that Boyle used to establish
what is today known as Boyle’s Law, which states the inverse relationship between the volume of
a gas and the pressure exerted on it. His experiments lent great support to the idea that air was
composed of discrete, rapidly moving ‘corpuscles’ (what we would call atoms or molecules) that
collide with the walls of their container and exert a pressure that Boyle called ‘the spring of the
air’.
In his book The Sceptical Chymist (1661) he defined elements as ‘certain primitive and simple,
or perfectly unmingled bodies’. He argued that the Aristotelian view that the elements should be
confined to earth, air, fire and water was not supported by observations. His primary goal was to
transform alchemy to make it more scientific by framing good hypotheses based on sound
experimental methods reported with great accuracy and detail. In London, Boyle established
another laboratory and, among other endeavours, was active in the isolation and production of
the new element: phosphorus. He was also a prolific writer of more than 40 books on a variety of
topics including chemistry as well as philosophy, medicine and religion. Boyle died in 1691 one
week after his beloved sister.
Glen E. Rodgers
1627
Born in Lismore, Ireland
1639
Sent on a Grand Tour to Paris, Geneva and Florence
1644
Returns to England after his father’s death and stays with his sister Katherine, Lady Ranelagh in
London, where they are members of the ‘Invisible College’
1645
Moves into his father’s manor in Stalbridge in Dorsetshire, England, where he sets up his first
laboratory
1654
Moves to Oxford where he again lives with his sister. He and his assistant Robert Hooke establish
a laboratory. Hooke builds a ‘pneumatic engine’
1661
Publishes The Sceptical Chymist, in which he strongly expresses his corpuscular or atomic
hypothesis and provides a definition of an element
1662
Publishes the second edition of The Spring of the Air, in which he establishes Boyle’s Law
1668
Moves back to London, where he and Hooke again establish a laboratory. By now the ‘Invisible
College’ has become the ‘Royal Society of London for Improving Natural Knowledge’
1691
Dies in London one week after his sister
CERAMICS
Ceramics are among the most important materials in human civilization. They are solids
held together by networks of ionic or covalent bonds extending throughout the material.
They differ from metals in that the bonds are to some extent directional and so must be
broken in order for planes of atoms to slip past one another. As a result, ceramics cannot be
easily deformed, as metals can, but instead tend to be brittle and hard. Ceramics may be
made by mixing finely powdered minerals and heating them until their atoms are moving
fast enough to move into each other or until the minerals melt into a single liquid phase.
When cooled, the atoms in the resulting ceramic are often aligned in the neat rows of a
crystal. Glasses may be produced if the cooling is fast enough so that the atoms are frozen
in a snapshot of the chaotic liquid from which they were made. Many alumino-silicate
mineral ceramics consist of covalently bonded chains or sheets that can absorb water and
metal ions in between the layers. These include clays that swell considerably when they
take up water, as well as the mineral kaolinite, which is a primary component of fine china
or porcelain.
3-SECOND NUCLEUS
The technologically useful properties of ceramic materials depend on the 3D arrangement of their atoms
and the nature of the chemical bonds holding them together.
3-MINUTE VALENCE
The first ceramic figurines and pots were made more than 20,000 years ago, long before metal tools. Later
artisans used tough ceramics like porcelain, clear ceramics like glass and the cements that dominate
cityscapes today. Ceramic scientists continue to produce new technologically useful materials: recent
examples include silicon carbide cutting tools, boron-nitride lubricants, silicon computer chips and
bioglass-based medical implants made from silica and hydroxyapatite.
RELATED TOPICS
See also
THE SOLID STATE
HERMANN SEGER
1839–93
German chemist who pioneered the scientific study of ceramics using the periodic table
RUSTUM ROY
1924–2010
Indian-born scientist who developed the sol-gel method for preparing ceramics from liquid chemical
precursors
W. DAVID KINGERY
1926–2000
American material scientist who first applied solid state chemistry principles to ceramic synthesis and
processing
30-SECOND TEXT
Stephen Contakes
The structure and bonding in ceramic materials determine their many useful
properties.
SOLUTIONS
Solutions are homogeneous mixtures formed when one substance (a solute) dissolves in
another substance (a solvent). Ocean water, air and sugar water are common examples of
solutions. Aqueous solutions are those in which water is the solvent. Solutions show
different properties from the components that compose them. For instance, a salt-water
solution has a lower freezing temperature than pure water (which is one reason why
freshwater lakes freeze more easily than oceans). Similarly, a salt-water solution has a
higher boiling temperature, lower vapour pressure and higher osmotic pressure when
compared to pure water. Such solution characteristics are known as ‘colligative properties’.
They were first studied experimentally by Richard Watson, a Professor of Chemistry at
Cambridge University, who observed the freezing time of a series of 18 aqueous solutions
of various salts exposed to an unusually cold (-14°C/6.8°F) February atmosphere in
Cambridge. He realized that the primary factor determining the degree of lowering in the
freezing point of a solution is the number of solute particles (concentration) and not the
type of salt. Calcium chloride (CaCl2) is more effective in treating icy roads than sodium
chloride (NaCl) because it provides more solute particles (ions) when mixed with the icy
surface.
3-SECOND NUCLEUS
When the particles of one substance are dissolved in a second (the solvent), they interfere with the way
the solvent molecules interact, changing the properties of the solution.
3-MINUTE VALENCE
The nature of intermolecular forces in all states of matter partly determines whether one substance
dissolves in another. The ‘like dissolves like’ principle is helpful in determining solubility in water: polar
solutes tend to be most soluble in water (since water is polar). For example, salt is soluble in water but
grease (mostly nonpolar) is not.
RELATED TOPICS
See also
THE GASEOUS STATE
THE LIQUID STATE
DAVID BERNOULLI
1700–82
Swiss mathematician whose work Hydrodynamica provided the first qualitative discussion of aqueous
salt solutions
RICHARD WATSON
1737–1816
Professor of Chemistry at the University of Cambridge who first carried out experimental measurements
studying the properties of aqueous salt solutions
30-SECOND TEXT
Ali O. Sezer
Salt water solutions have a lower freezing point than pure water, which is why
salt is used to reduce snow and ice build-up on roads and pathways.
CHEMICAL REACTIONS & ENERGETICS
CHEMICAL REACTIONS & ENERGETICS
GLOSSARY
acid A substance that produces H+ ions in solution. Acids neutralize bases, producing
water as a product.
base A substance that produces OH- ions in solution. Bases neutralize acids, producing
water as a product.
catalyst A substance that increases the rate of a reaction without being consumed by the
reaction.
chemical energy The energy that can be obtained from a chemical reaction when the
reactants have greater potential energy than the products.
chemical reaction A process in which the atoms in one or more substances (the reactants)
rearrange to form different substances (the products).
electrolysis The use of electrical current to drive a chemical reaction that would not
happen spontaneously.
electrolyte A substance that produces an electrically conductive solution when dissolved in

water.
entropy A thermodynamic quantity related to the amount of energy dispersed into a

substance at a given temperature.
enzyme A protein that acts as a biological catalyst to increase the rate of a biochemical
reaction.
exothermic A reaction that emits energy into the surroundings.
filtration A process of separation in which a solid is separated from a liquid using a

filtration device such as a funnel and filter paper.
greenhouse gas An atmospheric gas that is transparent to visible light, but absorbs infrared
light. These atmosphere gases act like glass in a greenhouse, allowing light to enter but
preventing heat energy from escaping. The three most important greenhouse gases in
Earth’s atmosphere are water vapour, carbon dioxide and methane.
hydrocarbon An organic compound containing only carbon and hydrogen.
Kelvin scale An absolute scale used for measuring temperature. On the Kelvin scale, water
freezes at 273 K and boils at 373 K. The lowest possible temperature (at which point
molecular motion stops) is zero on the Kelvin scale.
kinetic energy The energy associated with the motion of an object or particle.
neutralization A chemical reaction between an acid and a base that typically produces
water and a salt.
oxide An oxygen-containing compound.
potential energy The energy associated with the position (within a field) or composition of
an object.
precipitation A reaction between two solutions in which a solid (or precipitate) forms.
reactant Any one of the substances that undergoes a chemical reaction. In a reaction,
reactants react to form products.
thermal energy The energy associated with the random thermal motion of atoms and
molecules.
thermodynamics The study of energy and its conversions from one form to another.
transition-metal oxides Compounds containing a transition metal and oxygen.
voltaic cell A chemical cell that employs a spontaneous chemical reaction to produce
electrical current.
CHEMICAL EQUATIONS
Chemists must move seamlessly between three related worlds: the macroscopic world that
exists in the lab within beakers, flasks and test tubes; the atomic and molecular world,
which we can’t see but are constantly trying to imagine and understand; and the symbolic
world, which is how we represent the atomic and molecular world on paper. A chemical
equation is a way to symbolically represent changes that occur in the atomic and molecular
world. These changes are called chemical reactions and they often (although not always)
result in significant changes in the macroscopic world. For example, the burning of natural
gas is a chemical reaction. In this reaction methane gas combines with oxygen to form
carbon dioxide and water. In the macroscopic world, we see the reaction as a blue flame on
our stove top. In the molecular world, methane molecules combine with oxygen molecules
and transform into carbon dioxide molecules and water molecules. In the symbolic world,
we represent the reaction with the following chemical equation:
CH4 + 2 O2 → CO2 + 2 H2O.
Chemical equations must be balanced: they must contain the same number of each type of
atom on either side of the equation. Why? Because in a chemical reaction, matter is
conserved. Atoms can’t just vanish or form out of nothing.
3-SECOND NUCLEUS
A chemical equation is a way to precisely represent a chemical reaction, a change in which the atoms that
compose one or more substances rearrange to form one or more different substances.
3-MINUTE VALENCE
Chemical reactions occur all around us all the time. For example, our cars are powered by chemical
reactions; cooking is a chemical reaction; and our bodies maintain a myriad of reactions that allow us to
think, move, eat and reproduce. Chemical equations not only represent the identities of the reactants and
products in a chemical reaction; they also give us quantitative relationships between the amounts that
react.
RELATED TOPICS
See also
COMBUSTION REACTIONS & ENERGY SOURCES
NEUTRALIZING: ACIDS & BASES
ROBERT BOYLE
1627–91
Anglo-Irish chemist who formulated some of the earliest ideas about chemical reactions
ANTOINE LAVOISIER
1743–94
French chemist who contributed significantly to our understanding of chemical reactions, especially
combustion
30-SECOND TEXT
Nivaldo Tro
We witness chemical reactions, such as the burning of natural gas, every day.
COMBUSTION REACTIONS & ENERGY SOURCES
The first chemical reaction that early humans used was burning or combustion. In a
combustion reaction, a substance combines with oxygen and most commonly produces
carbon dioxide, water and other oxide products. Combustion reactions are useful because
they emit heat as they occur – they are exothermic. Certain molecules, especially
hydrocarbons, have an inherently high potential energy that can be released through
combustion. For this reason, our society’s fuels are largely based on hydrocarbons. Natural
gas is primarily methane (CH4). Liquefied petroleum (LP) gas is a mixture of propane
(C3H8) and butane (C4H10). Petrol is a mixture of hydrocarbons, such as octane (C8H18),
containing five or more carbon atoms. Coal is also a major part of our energy equation: it is
mostly carbon and combines with oxygen to form carbon dioxide. Together these fuels are
known as fossil fuels because they originated from ancient plant and animal life. However,
the combustion of fossil fuels is not without problems. The most vexing problem is
probably the emission of carbon dioxide, a greenhouse gas that is affecting Earth’s climate.
Since the Industrial Revolution, atmospheric carbon dioxide levels have risen by about 38
per cent, and average global temperatures have risen by about 0.8°C (1.4°F).
3-SECOND NUCLEUS
Our society’s energy comes largely from the combustion of fossil fuels, which produce large amounts of
energy when burned.
3-MINUTE VALENCE
Energy is critical to a society’s standard of living. In general, as the standard of living rises, so does energy
consumption. Our current energy sources are dwindling, however, and creating environmental problems.
The shift to alternative energy sources – such as solar power or wind power – has been slow, but steady.
The main challenges of the alternative sources are their cost and their inherent intermittence.
RELATED TOPICS
See also
CHEMICAL EQUATIONS
HYDROCARBONS
3-SECOND BIOGRAPHY
ANTOINE LAVOISIER
1743–94
French chemist who contributed significantly to our understanding of chemical reactions, especially
combustion
30-SECOND TEXT
Nivaldo Tro
Combustion or burning is common in energy generation and industry.
NEUTRALIZING: ACIDS & BASES
Most of us experience acids by taste – they are sour. Citrus fruits, vinegar, carbonated
beverages, yoghurt and sour sweets all owe their tangy deliciousness to the acids they
contain. Chemists prefer not to taste their work and often define acids as chemicals that
produce the hydrogen ion (H+) when dissolved in water. If acids are a chemical yin, then
bases are the yang. Bases tend to taste bitter and produce hydroxide (OH–) in water, the
chemical opposite of H+. When an acid and base are mixed, the hydrogen ion combines
with the hydroxide ion to form HOH (water):
H+ + OH– → H2O.
This type of chemical reaction is called neutralization. If exactly equal amounts of H+ and
OH– are mixed, the resulting solution will contain neither (because all of the H+ and OH–
ions reacted to form water), and it won’t be acidic or basic. Our stomachs use hydrochloric
acid (HCl) to help digest our food. If we eat too much, especially acidic or fatty foods, our
stomachs can produce too much HCl, causing us to feel uncomfortable (sometimes called
‘sour stomach’). To neutralize the excess acid, we can take an antacid. Antacids are bases
like aluminium hydroxide (Al(OH)3), magnesium hydroxide (Mg(OH)2) and calcium
carbonate (CaCO3) that neutralize the excess stomach acid.
3-SECOND NUCLEUS
Acids produced H+ in water while bases produce OH–. An acid and a base react to produce water,
effectively neutralizing each other.
3-MINUTE VALENCE
The pH scale is used to measure the acidity or basicity of a solution. The lower the pH value, the higher
the concentration of H+, and the more acidic the solution. The higher the pH value, the higher the
concentration of OH–, and the more basic the solution. Pure water is neutral and has a pH of 7. Stomach
acid is pH 1.6, tomato juice 4.2, sea water 8.2 and milk of magnesia (Mg(OH)2) 10.4.
RELATED TOPICS
See also
OPPOSITES ATTRACT
SOLUTIONS
CHEMICAL EQUATIONS
SVANTE ARRHENIUS
1859–1927
Swedish winner of the Nobel Prize for Chemistry (1903), who first suggested the acid/base definitions
given here
JOHANNES BRØNSTED & MARTIN LOWRY
1879–1947 & 1874–1936
Danish and British chemists who defined acids and bases on how they react
30-SECOND TEXT
Jeff C. Bryan
Antacids contain bases that neutralize stomach acid, the cause of heartburn.
CREATING SOLIDS: PRECIPITATION REACTIONS
Two friends are out for a night on the town, both looking for love. One is drawn to an
incredibly attractive stranger. Once together, the friend and the stranger never separate,
because the attraction is so strong. They drop out of sight, losing touch with their old
friends. This scenario is similar to a particular type of chemical reaction called a
precipitation reaction. When two or more ions are mixed in water, they are initially
attracted to nearby water molecules. However, as they move around (due to thermal
energy), the ions encounter each other and are drawn together. If the attraction is strong
enough, the two ions will stick together and fall out of solution (form a solid). If the
attraction isn’t very strong, the ions don’t get together and just stay in solution. As
examples, when silver (Ag+) and chloride (Cl–) are mixed they stick together and form a
solid precipitate. However, sodium (Na+) is much less attractive to chloride, so they don’t
form a precipitate. The ‘bathtub ring’ that you sometimes see if you bathe in hard water is
due to a precipitation reaction between the ions in hard water and the ions in soap.
3-SECOND NUCLEUS
A precipitation reaction occurs when two ions are so strongly attracted to each other that they form a
solid.
3-MINUTE VALENCE
Precipitation reactions are particularly useful when something needs to be removed from a solution. For
example, water treatment plants can use precipitation reactions to remove undesirable contaminants
from our water. If a chemical reaction takes place in a solution, and the product is insoluble in that
solution, then it falls out of solution as a solid and can be isolated by filtration.
RELATED TOPICS
See also
OPPOSITES ATTRACT
THE SOLID STATE
CERAMICS
3-SECOND BIOGRAPHY
LINUS PAULING
1901–94
American winner of the 1954 Nobel Prize in Chemistry, who developed our understanding of how atoms
and molecules are attracted to each other. He was also a peace activist and won the 1962 Nobel Peace
Prize
30-SECOND TEXT
Jeff C. Bryan
In a precipitation, a solid forms when two liquid solutions are mixed.
USING CHEMISTRY TO GENERATE ELECTRICITY
Chemical reactions in which electrons migrate from one chemical substance to another are
called oxidation-reduction reactions. These types of reactions can be used to generate
electricity by arranging the chemical substances so that the substance gaining electrons
(being reduced and called the oxidizing agent) is not in physical contact with the substance
losing electrons (being oxidized and called the reducing agent). The electrons are then
forced to travel through an external circuit to get from the reducing agent to the oxidizing
agent. This arrangement is called a voltaic cell. Self-contained voltaic cells – either by
themselves or connected in series – function as batteries. They produce electricity. The lead
storage battery used to start a car engine is comprised of six voltaic cells containing lead
and lead oxide immersed in a solution of sulfuric acid (battery acid). Dry cell batteries,
such as those used in torches, use zinc and magnesium dioxide. Button batteries (used in
calculators or watches) also use zinc, but they have mercuric oxide or silver oxide
substituted as the oxidizing agent. Lithium ion batteries use lithium between planes of
graphite as the reducing agent and a lithium metal oxide as the oxidizing agent.
3-SECOND NUCLEUS
Loss of electrons is oxidation, while gain of electrons is reduction; reactions that involve transfer of
electrons between reactants are oxidation-reduction or redox reactions.
3-MINUTE VALENCE
Corrosion results from oxidation of metals exposed to oxidizing agents in the environment. When the
metal is iron, the process is rusting. Rust is hydrated forms of iron(III) oxide generated when iron is
exposed to moisture and oxygen. The rate of rusting depends on the acidity of the environment and the
presence of electrolytes to help carry electric current. Having a metal that is more easily oxidized (a
sacrificial electrode) in contact with iron can retard rusting.
RELATED TOPIC
See also
CHEMICAL EQUATIONS
MICHAEL FARADAY
1791–1867
English scientist who developed the system of oxidation numbers and coined many terms associated with
electrochemistry
WALTHER HERMANN NERNST

1864–1941
German chemist who developed the equation for the relationship between concentration and voltage
30-SECOND TEXT
John B. Vincent
Batteries use chemical reactions that involve the transfer of electrons to

produce electricity.
REACTION RATES & CHEMICAL KINETICS
Chemical reactions occur at a variety of speeds or rates. Chemical explosions occur rapidly,
with the creation of large volumes of hot gas. Many chemicals are stable, however; they
react so slowly that they can be placed in a bottle. Fortunately, the rates (or speeds) at
which chemical reactions occur can be controlled – and studying these processes is the
field of chemical kinetics. One way to increase the rate of a reaction is by increasing the
temperature. For this reason, the reactions that cook food happen faster the higher the
temperature. Increasing the concentration of the reactant substances or surface area also
increases the rates of chemical reactions. You can hold an iron nail in your hand, but if it is
ground to a fine powder (greatly increasing its surface area) the iron can burst into flames
in air. The concentration of many chemicals in your body must be carefully regulated for
you to remain healthy. Your body accomplishes this by regulating the rates of a wide range
of chemical reactions. The rates of slow reactions are accelerated by proteins called
enzymes; these biological molecules are catalysts (substances that change the rate of a
chemical reaction without being consumed by the reaction).
3-SECOND NUCLEUS
The rate of a chemical reaction is the speed at which the reaction occurs and depends on reactant
concentration, temperature and whether or not a catalyst is present.
3-MINUTE VALENCE
Although nitrogen and oxygen gas are stable, at the temperature of a car engine they react to produce
nitric oxide gas (NO), an air pollutant that is a cause of acid rain and smog. NO is removed from a car’s
exhaust gas by a catalytic converter. In the converter, the exhaust passes over a honeycomb-like structure
of alumina impregnated with solid transition-metal oxides that catalyse the conversion of NO back to O2
and N2.
RELATED TOPICS
See also
CHEMICAL EQUATIONS
USING CHEMISTRY TO GENERATE ELECTRICITY
JACOBUS HENRICUS VAN ’T HOFF
1852–1911
Dutch chemist who won the first Nobel Prize in Chemistry in part for determining graphical methods to
establish that reaction rates depend on the concentrations of the reactants
HENRY TAUBE
1915–2005
American chemist who won the 1983 Nobel Prize in Chemistry for relating rates of chemical reactions to
electronic structure
30-SECOND TEXT
John B. Vincent
Controlling how fast a chemical reaction occurs allows us to reduce pollution

and create new molecules.
HUMPHRY DAVY
Humphry Davy, ‘full of mischief, with a

penchant for explosions … a born chemist’,
spent his youth fishing, hunting, reading,
storytelling and writing poetry. As a teenager
he loved fireworks and other explosive
chemical reactions. He was apprenticed to a
surgeon and apothecary, but reluctantly gave
this up to become director of Thomas
Beddoes’s Pneumatic Institute in Bristol. This
clinic, established to study the effect of gases
on improving human health, gave Davy the
opportunity to prepare, characterize and purify
nitrous oxide – which earlier researchers had
thought caused the plague. Davy was not
convinced and took a small whiff for himself.
Noting that he did not meet his demise, he
soon discovered that this sweet-smelling gas
was thoroughly intoxicating. Fellow partakers
giggled and laughed out loud, and Davy called it ‘laughing gas’.
In Bristol, Davy became friends with a broad cross-section of intellectuals. His good looks,
personal charm, and storytelling abilities, combined with his startling discoveries, made him a
rising star. Although it soon became clear that Beddoes’s clinic would be short-lived, Davy had
matured into an excellent chemist. Luckily he soon found an electrifying new field of study
occasioned by Alessandro Volta’s invention of a chemical battery, known then as a Voltaic pile.
Characteristically, one of the first things he did was to build his own pile and shock himself to
gauge its effectiveness!
In 1801, Davy was invited to be a lecturer at the newly minted Royal Institution in London.
Here he quickly produced a series of immensely popular lectures augmented by striking
demonstrations. He was an extremely handsome young man with a gift for working audiences, so
he attracted huge crowds that included many of the young ladies of that day. One such admirer
admitted that ‘those eyes were made for something besides poring over crucibles.’ Active in the
electrolysis of metal oxides, he discovered six elements (sodium, potassium, magnesium,
calcium, strontium and barium) in two years (1807–08) and became the leading chemist of his
day.
His penchant for self-experimentation caused debilitating injuries that resulted in his hiring of
Michael Faraday as his assistant. Davy often claimed that Faraday was his most important
‘discovery’. In 1812 Davy was knighted, married and embarked on a Grand Tour of Europe. Upon
his return he invented the coal miner’s safety lamp that saved many lives. He was essentially an
invalid for the last third of his life and died shortly after his 50th birthday. Nevertheless, during
his short and exciting lifetime, he was one of the best practitioners of and spokesmen for the new
science of chemistry.
Glen E. Rodgers
1778
Born in Penzance, in southwestern England
1795
Apprenticed to a surgeon and apothecary
1797
Studies chemistry by reading in French the recently guillotined Antoine Lavoisier’s Traité
élémentaire de chimie
1798
Becomes the director of Thomas Beddoes’ Pneumatic Institute in Bristol
1799
Prepares and imbibes nitrous oxide, which he nicknames ‘laughing gas’
1800
Publishes Researches, Chemical and Philosophical; chiefly concerning nitrous oxide or
dephlogisticated nitrous air, and its respiration
1800
The news of Alessandro Volta’s 1796 discovery of a chemical battery, known as the ‘Voltaic Pile’,
comes to England
1801
Invited to be a lecturer at the newly formed Royal Institution in London
1802
Appointed professor of chemistry at the Royal Institution; soon builds a giant Voltaic pile in the
basement
1807-1808
Using his Voltaic pile, discovers six elements (sodium, potassium, magnesium, calcium, strontium
and barium) in two years
1810
‘Discovers’ and launches Michael Faraday on a stellar chemistry career
1812
Knighted, marries, retires and with his new wife and Faraday, tours the continent visiting major
laboratories
1815
Invents the coal miner’s safety lamp
1829
After a lengthy period of debilitation, dies in Geneva, Switzerland
ENERGY & THE FIRST LAW OF THERMODYNAMICS
The universe has a quantity we call energy. Objects can possess it and can transfer it to
other objects, but it can neither be created nor destroyed. The total amount of energy that
exists is constant. This principle is known as the first law of thermodynamics. (A more
nuanced treatment includes mass/energy as the constant, but we simplify a bit here.) We
formally define energy as the capacity that an object has to exert a force on another object
across a distance. For example, a moving car has energy because it has the capacity to
strike another object and exert a force on it over a distance. Energy can come in many
different forms. The moving car has kinetic energy, the energy associated with its motion.
All substances above zero kelvin have thermal energy, a type of kinetic energy associated
with the random, temperature-dependent motion of the particles that compose the
substance. The higher the temperature, the greater the thermal energy. The book you are
holding contains potential energy, the energy associated with an object’s position.
Chemical substances have chemical energy, a type of potential energy associated with the
positions of all of their electrons and protons. Energy can be transferred or exchanged but,
according to the first law, it can never be created or destroyed.
3-SECOND NUCLEUS
Energy can be transferred or exchanged but, according to the first law of thermodynamics, it can never be
created or destroyed.
3-MINUTE VALENCE
The first law of thermodynamics implies that energy cannot be made out of nothing. Any human attempt
to create energy out of thin air has failed. The law has not, of course, prevented humans from trying. But
as far as we know, the spontaneous creation of energy is impossible. In other words, when it comes to
energy, you can’t win – you can’t get something for nothing.
RELATED TOPICS
See also
ENTROPY & THE THIRD LAW OF THERMODYNAMICS
ENTROPY & SPONTANEOUS PROCESSES
3-SECOND BIOGRAPHY
RUDOLF CLAUSIUS
1822–88
German physicist who formulated one of the earliest versions of the first law of thermodynamics
30-SECOND TEXT
Nivaldo Tro
A steam engine is powered by the energy transferred from burning fuel.
We have seen that in energy transactions, you can’t win – you can’t get energy out of
nothing. But it gets worse – you can’t even break even. In our universe, energy always
spreads out or randomizes itself as much as possible. The second law of thermodynamics
describes this pervasive tendency: in any spontaneous process, a quantity called entropy
(which you can think of as a measure of energy randomization or energy dispersion)
always increases. You have no doubt experienced the second law every time you hold a
warm drink. The thermal energy in the drink disperses itself into the surroundings – the
drink spontaneously cools down (and the air surrounding the drink warms up a bit).
Imagine a universe in which the hot drink gets hotter (and the surroundings slightly cooler)
as energy transfers from the surroundings into the drink! Not possible according to the
second law. The second law implies that, in any energy transaction, some energy must be
dispersed if the transaction is to occur at all. In other words, nature always takes a heat tax.
For example, recharging a battery will always take more energy than the amount of energy
you can use as you discharge the battery. Such is the second law – when it comes to energy,
you can’t break even.
3-SECOND NUCLEUS
For all spontaneous processes entropy increases.
3-MINUTE VALENCE
The second law of thermodynamics implies that a perpetual motion machine – one that keeps on moving
forever without the need for energy input – is impossible. With each cycle of the machine’s motion, some
energy must be dispersed in order for the motion to occur at all. As a result, the energy of the machine
must necessarily decrease over time, and it must eventually stop moving.
RELATED TOPICS
See also
NICOLAS LÉONARD SADI CARNOT
1796–1832
French physicist instrumental in the development of thermodynamics
RUDOLF CLAUSIUS
1822–88
German physicist who was instrumental in formulating the second law of thermodynamics
30-SECOND TEXT
Nivaldo Tro
A perpetual motion machine cannot exist according to the second law of

thermodynamics.
According to the first law of thermodynamics, you can’t win – you can’t get something for
nothing. According to the second law, you can’t break even – every energy transaction
necessarily results in a loss to the surroundings. According to the third law of
thermodynamics, you can’t get out of the game. In the case of thermodynamics ‘getting out
of the game’ means getting to the lowest possible temperature, zero kelvin or absolute zero.
Absolute zero is the temperature at which atomic and molecular motion essentially stops.
The third law of thermodynamics states that the entropy of a perfect crystal is zero at zero
kelvin. This law has two implications. The first one is that entropy, unlike other
thermodynamic quantities, can be measured on an absolute scale. All perfect crystals have
zero entropy at zero kelvin. As the temperature rises, energy is dispersed into the crystal
and its temperature and entropy increases. The second implication is that absolute zero can
never be reached in a finite number of steps. It would take an infinite number of cooling
steps to arrive at the absolute zero of temperature, so it can never be achieved.
3-SECOND NUCLEUS
The absolute entropy of a perfect crystal at zero kelvin is zero.
3-MINUTE VALENCE
Entropy is a measure of the energy dispersed into a system per unit temperature. For this reason,
dispersing the same amount of energy into a system at a colder temperature produces greater entropy
than dispersing that energy into a warmer system. As we will see in the next entry, this is the reason that
ice melts above its melting point but not below it.
RELATED TOPICS
See also
3-SECOND BIOGRAPHY
WALTHER HERMANN NERNST
1864–1941
German chemist who formulated the third law of thermodynamics and received the 1920 Nobel Prize in
Chemistry for his work
30-SECOND TEXT
Nivaldo Tro
The third law of thermodynamics, as formulated by Walther Nernst, implies
that the absolute zero of temperature cannot be reached.
The criteria for determining whether any process will happen is simple: will the process
result in an increase in entropy? Consider the freezing of water. Water freezes
spontaneously below 0°C (32°F). Why? When water freezes, the water molecules become
more organized, and the energy they contain becomes less randomized - their entropy
decreases. How then is this process ever spontaneous? Because when water freezes it gives
off heat (energy is dispersed) and the resulting entropy increase in the surroundings is
temperature-dependent. We can understand this with a simple analogy. If you give a poor
person £1,000, you significantly increase his or her net worth. But if you give a rich person
the same £1,000, the impact is negligible. Similarly, if you disperse a given amount of
energy into cold surroundings, you significantly increase its entropy, but if you disperse the
same amount of energy into warm surroundings, the increase is less. When the freezing of
water occurs below 0°C, the heat emitted into the surroundings is enough to increase the
entropy of the surroundings so much that it more than compensates for the decrease in
entropy of the water molecules themselves, resulting in an overall increase in entropy of
the universe and therefore a spontaneous process.
3-SECOND NUCLEUS
A process is spontaneous if it increases the entropy (energy dispersion) of the universe.
3-MINUTE VALENCE
Processes that result in a decrease in entropy are not impossible, they just don’t happen spontaneously.
Iron spontaneously reacts with oxygen to form iron oxide (rust). This process causes an increase in the
entropy of the universe. However, iron oxide can be turned back into iron. In fact, the manufacture of iron
metal from iron oxide depends on it.
RELATED TOPICS
See also
JOSIAH WILLARD GIBBS
1839–1903
American physicist who developed the main criteria for the spontaneity of a process
LUDWIG EDUARD BOLTZMANN

1844–1906
Austrian physicist who developed a statistical description of the second law of thermodynamics
30-SECOND TEXT
Nivaldo Tro
When ice melts at a temperature above its melting point, the entropy of the
universe increases.
INORGANIC CHEMISTRY
INORGANIC CHEMISTRY
GLOSSARY
allotropes Two or more forms of the same element, but with different structures (and
therefore different properties).
catalytic properties To have the ability to act as a catalyst (a substance that increases the
rate of chemical reaction without being consumed by the reaction).
CFCs Chlorofluorocarbons. These compounds were common in air conditioning and

refrigeration, but are now banned due to their harmful effect on the Earth’s ozone layer.
colour wheel A circle or wheel that contains different colours and shows how they are
related. You can use a colour wheel to predict the colour of an object based on what colours
the object absorbs.
complementary colours Two colours opposite each other on a colour wheel.

Complementary colours have high contrasts between one another.
complex (transition metal complex) A compound or ion consisting of a transition metal

linked to one or more ligands.
concatenated atoms Atoms that have been linked to form a chain structure.
crystal field theory (also ligand field theory) A bonding theory in inorganic chemistry in
which ligands donate an electron pair to a central metal ion.
diffraction grating A surface engraved with a series of closely spaced lines that reflects
different wavelengths of light at different angles. Diffraction gratings can split white light
up into its constituent colours.
electromagnetic spectrum The range of frequencies of electromagnetic radiation bounded

by radio waves at low frequencies and gamma rays at high frequencies.
fuel cell An electrochemical cell that produces electrical current from the continuous input
of a fuel.
fullerenes Carbon molecules that have spherical, tubular or other similar structures.
graphene A form of carbon consisting of a sheet of carbon atoms one atom thick.
graphite A form of carbon composed of carbon atoms bound together in sheets, which are
stacked on top of one another.
ligand A molecule or ion that donates an electron pair to a central metal ion in transition
metal complex.
metalloid An element that falls along the boundary between metals and non-metals on the
periodic table. Metalloids have properties intermediate between metals and non-metals.
oxidation state The charge an atom would have in a chemical compound if all of the
bonding electrons were assigned to the more electron negative atom (the atom that most
strongly attracts electrons).
photosynthesis The process by which plants convert carbon dioxide, water and sunlight
into glucose and oxygen.
prism A clear optical element that is usually triangular in shape and can bend light of
different wavelengths by different amounts. When white light travels through a prism, it is
broken up into its constituent colours.
reactant Any one of the substances that undergoes a chemical reaction. In a reaction,
reactants react to form products.
silicate Compound containing silicon, oxygen and sometimes various metal atoms.
Silicates form network covalent structures with high melting points.
stratosphere An atmospheric layer that begins about 10 km (just over 6 miles) above the
Earth’s surface and is sandwiched between the troposphere below and the mesosphere
above.
substrate The molecule on which an enzyme (a biological catalyst) acts.
transition metals Those metals found in the large centre block of the periodic table (the d-
block). Transition metals (in contrast to main group metals) tend to have properties that are
less predictable based on their exact position on the periodic table.
valence electrons The highest energy electrons (and therefore the most important in
bonding) in an atom.
Zintl ions Ionic clusters of main group elements.

THE UNIQUENESS PRINCIPLE
The periodic table contains a dividing line that is never marked. The invisible line occurs
between the table’s second and third rows, where boron meets aluminium; carbon meets
silicon; and so on until fluorine meets chlorine. Elements above the line cannot form bonds
to as many atoms as those below the line, being strictly limited to a total of eight ‘valence’
or bonding-level electrons. Thus, while oxygen forms the mono- and dioxides with itself
(that is, O2 and O3), sulfur, selenium and tellurium form mono-, di- and trioxides, of which
SO, SO2 and SO3 are examples. Similarly, nitrogen forms the trichloride NCl3 while
phosphorous, arsenic and antimony form both tri- and pentachlorides such as PCl3 and
PCl5. However, unlike later elements, the non-metals of the second row are small enough
to form strong multiple bonds, a quality that enables them to form compact molecules
where a heavier element would form an extended structure of linked atoms. Carbon, for
instance, forms the triple and doubly bonded oxides CO and CO2, while its heavier
counterparts – silicon, germanium, tin and lead – react with oxygen to form three-
dimensional solid networks held together exclusively by single bonds.
3-SECOND NUCLEUS
Elements in the periodic table’s second row behave differently from heavier elements because they form
strong multiple bonds and are limited to eight valence electrons.
3-MINUTE VALENCE
One consequence of the uniqueness principle is that planetary atmospheres largely consist of first- and
second-row elements. Earth’s atmosphere is comprised mostly of nitrogen and oxygen; Mars’s
atmosphere mostly of CO2; and those of the gas giants are mostly hydrogen, helium, CH4 and NH3. In
contrast, the planetary crusts of planets such as Earth and Mars contain large amounts of silicate
minerals, many of which contain chains, sheets and 3D networks held together by silicon-oxygen single
bonds.
RELATED TOPICS
See also
PERIODIC PATTERNS
CARBON: IT’S NOT JUST FOR PENCILS
VICTOR GOLDSCHMIDT
1888–1947
Swiss crystal chemist who classified elements by their dominant geologic locations
THOM DUNNING
1943–
American chemist who explained first-row anomalies in terms of recoupled pair bonds
30-SECOND TEXT
Stephen Contakes
The second-row elements are unique – they are very different from the
elements that lie below them in the periodic table.
COLOUR
When white light passes through a prism, the light is dispersed into a spectrum of colours.
The colours range from red at the lowest frequencies through orange, yellow, green, blue
and finally violet at the highest. Substances that absorb all frequencies of visible light
appear black, while substances that reflect all frequencies of visible light appear white.
Coloured objects appear to an observer to have a colour because they absorb certain
frequencies (or wavelengths) of visible light while reflecting or transmitting (allowing to
pass) others. The precise colour a substance has depends on which frequencies are
absorbed. In general, a substance will appear to have a colour complementary to the one
absorbed (and opposite it on a colour wheel). For example, a substance that appears yellow
absorbs violet light (the complement of yellow). Transition metal complexes are often
deeply coloured because they strongly absorb certain frequencies of light in the visible
region. These complexes often have unfilled outer-level orbitals that can receive an
electron excited by specific frequencies of visible light. The colour absorbed depends on
the separations between the d-orbitals, which in turn depend on the ligands attached to the
metal.
3-SECOND NUCLEUS
Coloured objects appear to have colour because they absorb some frequencies of visible light and reflect
or transmit the others.
3-MINUTE VALENCE
Our eyes can detect a narrow range of frequencies in the electromagnetic spectrum. This range of
frequencies is responsible for all of the colours that we see. Our brains have evolved to use colour as a
way to help distinguish one substance from another. Modern spectrometers, which precisely measure the
frequencies absorbed by substances, are among the most powerful scientific tools in substance
identification.
RELATED TOPICS
See also
CLUSTER CHEMISTRY
TRANSITION METAL CATALYSTS
ALFRED WERNER
1866–1919
Swiss chemist who won the 1913 Nobel Prize in Chemistry for predicting the three-dimensional structure
of many transition metal complexes before modern structural methods
JOHN HASBROUCK VAN VLECK

1899–1980
American physicist who won the 1977 Nobel Prize in Physics and was instrumental in the development of
crystal field theory, the precursor to ligand field theory
30-SECOND TEXT
John B. Vincent
White light separates into its component colours when passed through a prism.
CLUSTER CHEMISTRY
In some molecules, ions and materials the electrons that hold the atoms together are shared
between a group of clustered atoms. For instance, some metals and metalloids can be
reduced to liquid-soluble fragments of metal while many transition metals form clusters
when combined with chlorine, sulfur or carbon monoxide under the right conditions. Some
of the latter clusters catalyze commercially important reactions, although none has yet
found industrial use. Sometimes clusters exist as discrete units; in other cases they are
linked together in a network. Solid MoCl2, for example, consists of octahedral clusters of
Mo6Cl84+ bridged by intervening Cl- ions. However, when heated in the presence of
additional chloride, the connections are broken to give discrete Mo6Cl142- units. The ratio
of electrons to atoms in a cluster affects its shape. When clusters have just enough
electrons to hold together, they form as compact a shape as possible – that of the smallest
polyhedron that can accommodate all the core atoms. In contrast, clusters with more
electrons tend to open up and take on the shape of larger polyhedra with unoccupied
vertices, giving clusters that sometimes look like a molecular nest or a web.
3-SECOND NUCLEUS
Cluster compounds form when atoms and ions share electrons and bunch together in a polyhedral shape.
3-MINUTE VALENCE
Many of the most important reactions for life on Earth are facilitated by metal-containing clusters located
within proteins. For example, clusters containing iron and sulfur facilitate the movement of electrons
through many biological systems, including the respiratory chain our cells use to harvest energy by
converting oxygen to water. In photosynthesis plants reverse this process, harvesting even more energy
from sunlight to produce oxygen at a cluster containing four manganese ions and one calcium ion.
RELATED TOPICS
See also
NANOTECHNOLOGY
WILLIAM N. LIPSCOMB
1919–2011
American chemist who pioneered study of the structure and bonding in borane clusters
KENNETH WADE
1932–2014
British chemist who developed ‘Wade’s Rules’ for predicting cluster compounds’ shapes and stability
30-SECOND TEXT
Stephen Contakes
Cluster compounds have polyhedral shapes and unique properties.

TRANSITION METAL CATALYSTS
Many industrial chemicals are produced by combining small organic molecules or

substrates with catalysts composed of transition metals (such as cobalt, chromium or iron)
which are themselves bound to small molecules called ligands. In these processes the
metals speed up reactions between the substrates by acting as platforms where substrates
can bind and then break into smaller molecular fragments, rearrange how their atoms are
bound together and form new bonds with other substrates. The new molecules and
fragments that result can then be released from the metal to yield the reaction products and
regenerate the original metal complex. In fact, from the viewpoint of the metal the entire
process involves a cyclic series of reactions or ‘catalytic cycle’ in which the metal complex
adds reactants and spits out products. Some metal catalysts do not even need to bind their
substrates, but instead function by pushing electrons around. For instance, some biological
iron clusters facilitate the movement of electrons between reactants, alternatively gaining
an electron from one substrate and passing it to another. Other complexes can harvest
energy from light and use it to push electrons into or out of molecules, generating unstable
intermediates that then quickly react with other nearby molecules.
3-SECOND NUCLEUS
Transition metal compounds facilitate chemical reactions between small molecules that bind to the
metal, rearrange and get released as new products.
3-MINUTE VALENCE
Many biological and industrial processes involve transition metals acting as catalysts, substances that
speed up chemical reactions without being changed themselves. Without metal catalysts we could not
use the oxygen we breathe or produce enough food to sustain current population levels. Perhaps we
wouldn’t even be around today, because one hypothesis about the origin of life involves catalysis by iron
minerals.
RELATED TOPICS
See also
COLOUR
AMINO ACIDS & PROTEINS
HUMPHRY DAVY
1779–1829
British chemist who discovered that platinum was useful as a heterogeneous catalyst
KARL ZIEGLER & GIULIO NATTA

1898–1973 & 1903–79
German and Italian chemists who developed a catalyst for making commercial plastics with specific
properties
30-SECOND TEXT
Stephen Contakes
Transition metal compounds can act as catalysts in chemical reactions.

MARIO J. MOLINA
Born to a Mexican family of highly educated

professionals, Mario J. Molina is a Nobel Prize-winning
chemist whose work on the detrimental effects of
chlorofluorocarbons (CFCs) – a class of industrial
chemicals commonly used in refrigeration, aerosol cans
and plastic manufacturing – on the stratospheric ozone
layer provides an excellent example of how fundamental
research can have tremendous practical implications,
greatly improving the quality of life on Earth. His
research findings, published in the journal Nature in
1974, led to an international ban on CFC emissions into
the atmosphere (the 1985 Vienna Convention and the
Montreal Amendment).
Encouraged by his aunt Esther Molina, also a chemist,
Mario developed a strong fascination with natural
sciences, which became stronger when he observed the
living organisms in a drop of pond water with his first microscope. This thrilling experience drew
him to acquire chemistry sets and to build his own laboratory in an unused bathroom of his
family home. Recognizing how excited he was about chemistry, Molina’s parents briefly sent him
to a Swiss boarding school at the age of 11 to learn German, a language then quite useful for a
successful career in chemistry.
After studying chemical engineering at the Autonomous National University of Mexico, Molina
spent more than two years in Germany and France strengthening his engineering and
mathematics knowledge before completing his doctoral degree under the supervision of
Professor George Pimentel at the University of California, Berkeley.
In 1973, Molina joined Professor Rowland’s group as a postdoctoral researcher at the
University of California, Irvine, where he discovered that CFCs break down in the stratosphere,
producing elemental chlorine, which destroys the ozone layer that protects living things on Earth
from the Sun’s dangerous rays. Molina and Rowland met with fierce opposition from industrial
producers of CFCs until the British Antarctic Survey detected a large and growing gap in the ozone
layer in 1985. Molina, now a full-time researcher at the Jet Propulsion Laboratory at the
California Institute of Technology, further demonstrated that polar ice crystals in the
stratosphere amplified the destructive effect of CFCs on the ozone layer. By the end of 1985, most
of the CFC-producing countries signed the Vienna Convention, which was soon amended by the
Montreal Protocol, to end CFC emissions into the atmosphere. Mario Molina received the 1995
Nobel Prize in Chemistry for ‘contributing to our salvation from a potential global environmental
catastrophe’.
Ali O. Sezer
19 March 1943
Born in Mexico City, Mexico
1972
Receives his PhD in chemistry from the University of California, Berkeley
1973
Joins Professor Rowland’s research group at the University of California, Irvine
1974
Co-authors a paper in the journal Nature highlighting the damaging effects of CFCs to the ozone
layer in the stratosphere
1982
Moves to the Jet Propulsion Laboratory at the California Institute of Technology to carry out
experiments on the effect of CFCs on the ozone layer
1985
Demonstrates that ice crystals in the polar stratosphere amplify the ozone destruction capability
of CFCs
1989
Moves to Massachusetts Institute of Technology to continue his research in atmospheric sciences
1995
Receives the Nobel Prize in Chemistry for ‘contributing to our salvation from a potential global
environmental catastrophe’
2005
Moves to the University of California, San Diego, and the Centre of Atmospheric Sciences at
Scripps Institution of Oceanography
2013
Receives the Presidential Award of Freedom from President Obama
The major common allotropes of carbon include shiny, transparent and super-hard diamond
and soft black graphite. Graphene (isolated in 2010 by Andre Geim) is a one-atom-thick
sheet of carbon atoms densely packed into a chicken-wire-shaped structure. Graphite is
many sheets of these graphene layers stacked together. Since these layers are only weakly
bound to each other they are readily rubbed off onto paper and therefore used in pencils. In
1985, Harry Kroto discovered a new form of carbon (C60) when he and his colleagues
Richard Smalley and Robert Curl simulated chemical reactions that might occur in the
atmosphere of red giant stars. C60 is one of a larger family of carbon forms known as
fullerenes. Fullerenes are molecules in the form of hollow spheres, ellipsoids or cylinders.
Since C60 looks much like the famous geodesic domes of R. Buckminster Fuller, it was
dubbed ‘buckminsterfullerene’. Spherical or ellipsoidal fullerenes are fondly known as
‘buckyballs’. Graphene layers can also wrap around and form cylindrical tubes called
‘nanotubes’ or ‘buckytubes’. Fullerenes are flexible, strong and stable, with an ever-
increasing number of practical uses – for example, as catalysts, in energy generation and
storage devices, as MRI and X-ray contrast agents and in flexible electronics.
3-SECOND NUCLEUS
Carbon allotropes include diamond, graphite and fullerenes. Fullerenes, named after Buckminster Fuller,
come in the form of hollow spheroids (‘buckyballs’) and nanotubes (‘buckytubes’).
3-MINUTE VALENCE
Carbon is a unique element. Not only is it the central element on which all life is based, but in its
elemental state it also exists in several fascinating and useful allotropes (different molecular forms of a
given element).
RELATED TOPICS
See also
R. BUCKMINSTER FULLER
1895–1983
American inventor, architect and author who popularized the geodesic dome
HARRY KROTO
1939–2016
English chemist, winner of the 1996 Nobel Prize in Chemistry for discovering fullerenes
30-SECOND TEXT
Glen E. Rodgers
Carbon comes in many forms including familiar graphite and new forms such
as graphene.
NANOTECHNOLOGY
Nanotechnology is the study of matter where the basic structure has at least one of its
dimensions less than or equal to 100 nanometres (1 nanometre is one-billionth of a metre.)
This would therefore include almost all of chemistry, since most molecules meet such a
requirement. However, what is different about nanochemistry is that it uses bottom-up
molecular routes to reach the larger domains, coupling molecule to molecule to make larger
structures. This is in contrast to the traditional top-down approaches in which large
structures are cut into smaller pieces. The bottom-up route permits the precision of
chemical synthesis to affect larger materials properties. As an example of this bottom-up
approach, different molecules that are about 0.1 nanometre in size can be attached together
using synthetic chemical techniques to make tiny structures such as nanocars. A single
nanocar is 2 nm x 3 nm in size with four wheels, fully rotating axles, chassis and light-
activated motors. These nanocars may be able to perform work, such as bringing in
molecules or atoms through selective voltage pulse commands to further construct larger
entities or to deliver drugs to cells. Molecularly built nanocars are so small that 25,000 of
them lined up end to end would only span a distance the diameter of a human hair.
3-SECOND NUCLEUS
Nanotechnology is the science of building tiny structures from the molecular size up.
3-MINUTE VALENCE
Nanochemistry can also be used to construct nanoparticles of precise size and shape with unique
catalytic properties for processes such as converting hydrogen and oxygen to water in a fuel cell to
generate electricity. Other nanoparticles can be used to split water, using sunlight, to the requisite
hydrogen and oxygen needed by the fuel cell. Combined, such a system could potentially supply the
world’s energy needs in a far cleaner manner than using fossil fuels – as we do today.
RELATED TOPICS
See also
CLUSTER CHEMISTRY
RICHARD FEYNMAN
1918–88
American physicist who first suggested building molecular structures one atom at a time; he won the 1965
Nobel Prize in Physics
RICHARD SMALLEY
1943–2005
American chemist and foundational figure in nanotechnology who was awarded a share of the 1996 Nobel
Prize in Chemistry
30-SECOND TEXT
James Tour
Molecular machines such as nanocars have the potential to perform vital tasks
in medicine and energy supply.
ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
GLOSSARY
aldehydes A family of organic compounds containing a terminal C=O functional group.
aldosterone A hormone responsible for the regulation of sodium and potassium.
alkaloids Organic bases found in plants; often poisonous.
amines Organic compounds containing a nitrogen atom bonded to one or more carbon
atoms.
aromatic ring A flat, ring-shaped chain of carbon atoms containing alternating single and
double bonds.
carbonyl The C=O functional group.
carboxylic acid An organic compound containing the–COOH functional group.
covalent bond The joining of atoms by the sharing of one or more electrons.
cross-linked structure A common structure in polymers in which long chain-like

molecules form bonds between the neighbouring chains.
cyclic structures Any structure containing one or more rings of atoms bonded together.
distillation A process by which a mixture of compounds with differing boiling points can
be separated by heating the mixture and recondensing the gases that vaporize.
ester An organic compound containing the –COO –functional group.
functional group A characteristic atom or group of atoms present in a family of organic

compounds that give the compounds certain characteristics.
homologous series A series of organic compounds that differ in length by one carbon
atom.
hydrocarbon An organic compound containing only carbon and hydrogen.
hydroxyl group An –OH group characteristic of the organic family of alcohols.
isomers Two molecules with the same chemical formula but different structures.
ketone A family of organic compounds that contain the C=O functional group sandwiched
between two other carbon atoms.
linear structure A chemical structure in which the atoms that compose the structure fall
on a continuous line.
macromolecule A very large molecule, such as a polymer, typically containing thousands
of atoms.
molar mass The mass of one mole of an element or compound.
monomer Repeating unit in a polymer.
organic compounds Compounds that contain carbon bonded to hydrogen, nitrogen,

oxygen or sulfur.
paraffin wax A soft, flammable solid composed of a mix of long chain hydrocarbons.
progesterone A female sex hormone with the formula C21H30O2 that plays a role in the
menstrual cycle and pregnancy.
testosterone A male sex hormone with the formula C19H28O2.

ORGANIC CHEMISTRY & VITALISM
Early chemists divided compounds into two distinct types: organic and inorganic. Organic
compounds were isolated from living organisms and tended to be quite fragile. For
example, sugar is an organic compound (isolated from sugar cane or the sugar beet). If you
heat sugar in a pan, it quickly decomposes. Inorganic compounds came from the Earth and
tended to be more durable. For example, table salt is an inorganic compound (isolated from
salt mines or from oceans). If you heat salt in a pan, the salt does not decompose – you
simply get hot salt. Furthering the divide, early chemists were able to synthesize inorganic
compounds in the laboratory, but not organic compounds. This divide fitted well with an
eighteenth-century belief called vitalism, which suggested that all living organisms
contained a vital force that separated them from non-living things. The vital force allowed
living organisms to synthesize organic compounds, but a chemist could not synthesize an
organic compound in a beaker because no vital force was present. Vitalism died a slow
death in the middle of the nineteenth century because chemists began to synthesize organic
compounds from inorganic ones. Today, hundreds of thousands of organic compounds have
been synthesized, including many compounds central to life itself.
3-SECOND NUCLEUS
Vitalism, the belief that living things contained some unique force not contained in non-living things, was
proved false and abandoned in the nineteenth century.
3-MINUTE VALENCE
The downfall of vitalism is significant because it meant that living things could be studied from a chemical
point of view. The reactions that happen in living organisms are not qualitatively different from those that
happen outside of living organisms. The revolution that has occurred in biology over the last half-century
is largely due to understanding life from a molecular perspective.
RELATED TOPICS
See also
HYDROCARBONS
ALCOHOLS
ALDEHYDES, KETONES & ESTERS
GEORG ERNST STAHL
1659–1734
German chemist and advocate of vitalism
FREDERICH WÖHLER
1800–82
German chemist who, in 1828, synthesized urea, an organic compound, from inorganic starting materials
30-SECOND TEXT
Nivaldo Tro
Urea (centre) was one of the first organic compounds synthesized from
inorganic compounds.
HYDROCARBONS
Hydrocarbons, the principle constituents of petroleum and natural gas, are organic
compounds of hydrogen and carbon. Because carbon can bond, not only to other atoms like
hydrogen, but also to itself (a process called ‘catenation’), there are many naturally
occurring and synthetically produced hydrocarbon compounds. Hydrocarbons have had an
unmatched influence on the economic, social and environmental development of modern
society. They are a convenient source of energy and the starting materials to make many
common products such as polymers, textiles and pharmaceuticals. Hydrocarbons in all
physical forms find their way into our lives every day – in gas (natural gas), liquid (petrol)
and solid (paraffin wax) forms. They are, in general, classified as ‘saturated’ (only single
covalent bonds are present), ‘unsaturated’ (at least one double or triple covalent bond exists
between carbon atoms) or ‘aromatic’ (at least one aromatic ring is present). Long chains of
hydrocarbons can form linear, cross-linked or cyclic structures, with the number of carbon
atoms ranging from one (methane) to thousands. Hydrocarbons have high potential energy,
which can be released upon combustion – generating energy convenient for applications
such as transportation and heating.
3-SECOND NUCLEUS
Petrol, a potpourri of many hydrocarbons, packs a large amount of energy in a small volume, which
makes it a convenient source of fuel for transportation.
3-MINUTE VALENCE
Hydrocarbon-based ‘fossil fuels’ provide more than 80 per cent of the world’s energy – mainly as coal,
petroleum and natural gas. They are the most convenient and economical sources of energy for most
practical applications. However, hydrocarbons are non-renewable, with limited resources globally. The
search for alternative and renewable sources of energy will reduce the global dependence on fossil fuels
and help reduce their adverse impact on the environment.
RELATED TOPICS
See also
JAMES YOUNG
1811–83
Scottish chemist known as the father of the petrochemical industry who first distilled paraffin, a saturated
hydrocarbon, from petroleum
EDWIN L. DRAKE
1819–80
An American railroad conductor credited with drilling the first modern oil well, near Titusville,
Pennsylvania
30-SECOND TEXT
Ali O. Sezer
Petroleum is separated into its hydrocarbon components due to the differences

in the boiling points of those components.
ALCOHOLS
Isopropanol (C3H7OH), a popular antiseptic known as rubbing alcohol, and ethanol

(C2H5OH), the intoxicating component of alcoholic drinks, belong to a very important
class of organic compounds called alcohols. Alcohols contain the hydroxyl (–OH)
functional group. The smaller alcohols are clear, volatile and flammable liquids with a
biting odour. The alcohol family contains a homologous series of compounds from
hydrocarbons in which a hydrogen atom is replaced by an –OH group. Methanol, ethanol
and propanol are the first three members of this series. The –OH functional group is
directly bonded to a carbon atom, which is also connected to one (primary alcohol), two
(secondary alcohol) or three (tertiary alcohol) other carbon atoms. Ethanol and isopropanol
are examples of primary and secondary alcohols, respectively. The –OH group makes
alcohols highly polar, and the smaller ones are all miscible with water – meaning that they
form homogenous solutions with water in all proportions. Water-solubility decreases
noticeably as the number of carbon atoms (molecular mass) increases. Today alcohols find
a wide range of uses, from perfume-making through food and pharmaceutical products to
medical applications.
3-SECOND NUCLEUS
Beyond being the intoxicating component of alcoholic drinks, alcohols have an important place in organic
chemistry – with many applications benefitting human life.
3-MINUTE VALENCE
Polyalcohols, also known as sugar alcohols, are alcohols with more than one –OH group in their
molecular structure. These white, water-soluble solid compounds are industrially important – they are
used as thickeners and sweeteners. Sorbitol, erythritol, xylitol and maltitol are popular polyalcohols
commonly used in hard candy and artificial sweeteners. They do not get completely absorbed into the
bloodstream so they are incapable of rapidly raising blood sugar.
RELATED TOPICS
See also
OPPOSITES ATTRACT
HYDROCARBONS
JOHANN TOBIAS LOWITZ
1757–1804
German-born Russian chemist who first obtained pure ethanol by filtering distilled ethanol through
activated carbon
ARCHIBALD SCOTT COUPER

1831–92
Scottish chemist who first published the structural formula of ethanol, one of the first structural formulas
determined
30-SECOND TEXT
Ali O. Sezer
Alcohols are a common family of organic compounds that includes substances

such as ethanol (the alcohol in alcoholic beverages).
The pleasant odour and flavour of fresh almonds and peppermint are mainly due to
benzaldehyde and menthone, two naturally occurring compounds whose molecule contains
the carbonyl functional group (–C=O). Benzaldehyde is an example of a family of organic
compounds called aldehydes. In an aldehyde, the –C=O group is at the end of a carbon
chain. Menthone is an example of a family of organic compounds called ketones. In a
ketone, the carbonyl group is in the middle of the carbon chain. Another common family of
organic compounds is the ester family. In an ester, an oxygen atom interrupts the bonding
of the carbonyl group to the carbon chain (–CO2C–). Benzyl acetate, a component in the
smell of strawberries, pears and jasmine, is an ester. Small aldehydes and ketones (those
with low molar masses), such as formaldehyde (an important industrial solvent) and
acetone (nail-polish remover), have a strongly pungent odour. But aldehydes with
increasing molar masses generally have more pleasant and fruity odours. Aldehydes,
ketones and esters are commonly found naturally and manufactured industrially as odours
and flavours in food and pharmaceutical products. Many solvents used in adhesives, paints,
perfumes, plastics and fabrics also contain aldehydes, ketones and esters.
3-SECOND NUCLEUS
Aldehydes, ketones and esters are naturally occurring organic compounds responsible for the pleasant
odours and flavours of many natural and synthetic products.
3-MINUTE VALENCE
Aldehydes, ketones and esters are found abundantly in living organisms. Humans and animals store
energy as esters known as fats and oils. Testosterone and progesterone (the male and female sex
hormones, respectively), aldosterone (which regulates blood sodium level) and pheromone (which is
released by animals to trigger a social response) are all ketones. Retinal (retinaldehyde) is an aldehyde
forming the basis of vision. Acetaldehyde causes the ‘hangover’ feeling after alcohol is metabolized in the
liver.
RELATED TOPICS
See also
ALCOHOLS
CARBOXYLIC ACIDS & AMINES
LEOPOLD GMELIN
1788–1853
German chemist who first introduced the terms ‘ester’ and ‘ketone’
JUSTUS VON LIEBIG

1803–73
German chemist considered the father of organic chemistry, who first used the term ‘aldehyde’
30-SECOND TEXT
Ali O. Sezer
Many of the odours you smell every day come from the naturally occurring
families of aldehydes, ketones and esters.
Carboxylic acids and amines are important and familiar families of organic compounds.
Carboxylic acids are organic acids and can be identified by their –COOH functional group.
Like all acids, carboxylic acids taste sour. Acetic acid, the active component of vinegar, is a
carboxylic acid. The word vinegar originates from the French for wine (vin) and sour
(aigre). When wine is left exposed to air, the ethanol oxidizes to form carboxylic acid,
ruining the wine. Citric acid is another carboxylic acid; it is responsible for the sour taste of
lemons and limes. Amines are organic bases and contain a nitrogen atom bonded to one or
more carbon atoms. Many amines have an unpleasant odour. When living things die, their
proteins are broken down into amines, which evaporate into the air. For example, the smell
of rotting fish is due to trimethylamine, and that of decaying animal flesh to caderverine,
both foul-smelling amines. Some plant-based amines, known as alkaloids, have the ability
to alter sensory pathways. Caffeine, nicotine and cocaine are all alkaloids that stimulate the
central nervous system, resulting in feelings of increased alertness and energy. Other
alkaloids, such as morphine and codeine, have the opposite effect: they depress the central
nervous system. Morphine is a powerful depressant used to treat extreme pain.
3-SECOND NUCLEUS
Carboxylic acids and amines are naturally occurring acids and bases, respectively.
3-MINUTE VALENCE
The reaction between a carboxylic acid and an amine is an acid-base reaction that links the two
molecules together and forms water as a byproduct. This reaction is important in biochemistry because it
is responsible for the linking of amino acids – which are molecules that have a carboxylic acid group on
one side and an amine group on the other – to form proteins, the workhorse molecules in living
organisms.
RELATED TOPICS
See also
ALCOHOLS
3-SECOND BIOGRAPHY
HERMANN KOLBE
1818–84
German chemist who greatly contributed to the development of organic chemistry and was the first to
synthesize acetic acid
30-SECOND TEXT
Nivaldo Tro
Acetic acid (top) is responsible for the smell of vinegar. Trimethylamine

(bottom) is responsible for the foul smell of rotten fish.
FRIEDRICH WÖHLER
Friedrich Wöhler is known not only for his pioneering

research in chemistry but also for his model teaching
laboratories that revolutionized how experimental
chemistry is taught around the world today. His interest
in chemistry and mineralogy developed in the early years
of his education in Frankfurt, Germany. Although Wöhler
went on to receive a medical degree from the University
of Heidelberg, his real interest was always in chemistry.
Leopold Gmelin, one of the best-known chemists of the
nineteenth century, was Wöhler’s instructor at
Heidelberg. He quickly realized that Wöhler was too
advanced for his courses and sent him to study with Jons
Jacob Berzelius, the world-famous Swedish chemist who
is considered to be one of the fathers of modern
chemistry.
Wöhler spent a year studying mineralogy with
Berzelius. He not only received the best available education but also developed a life-long
friendship with his tutor. Wöhler later translated much of Berzelius’s work into German, including
his well-known Textbook of Chemistry. Wöhler himself wrote a number of textbooks on organic
and inorganic chemistry later in his career, including Outlines of Organic Chemistry in 1840.
Wöhler returned to Germany in 1825, and took a position at the newly founded Berlin
Gewerbeschule (trade school), where he conducted ground-breaking research that won him
international fame. In 1827 he isolated pure aluminium for the first time from its compounds. The
following year, he announced his second discovery in a famous letter to Berzelius, where he
explained how he had synthetically isolated urea in the laboratory without the need of a living
kidney, and that this compound had the same chemical composition as another compound called
ammonium cyanate. This discovery was significant, as researchers then believed that a ‘vital
force’ in living things was necessary to make organic compounds.
Two years after Wöhler’s letter, Berzelius explained these discoveries and coined the term
isomerism, a tremendously important concept in modern chemistry. From 1832 until his death in
1882, Wöhler served as a chemistry professor at the University of Göttingen, where he developed,
in parallel with Justus Freiherr von Liebig at the University of Giessen, today’s widely adopted
laboratory-based methods of science teaching. Wöhler is also credited with having inaugurated
the tradition of establishing scientific research groups in which students can also carry out
research activities.
Ali O. Sezer
31 July 1800
Born in Eschersheim, Germany
1823
Receives a medical degree from the University of Heidelberg, Germany
1827
Prepares the first pure sample of aluminium from its compounds
1828
Discovers how to make urea synthetically in the laboratory and isolates the elements beryllium
and yttrium
1832
Starts working as a chemistry professor at the University of Göttingen, Germany
1834
Elected foreign member of the Royal Swedish Academy of Sciences
1854
Elected foreign member of the Royal Society of London
1855
Elected member of the Royal Academy of Berlin
1862
Produces calcium carbide and acetylene gas
1872
Awarded the Copley Medal by the Royal Society of London
23 September 1882
Dies in Göttingen, Germany
CHEMISTRY COPYING NATURE
The Pacific yew tree is rather unremarkable. It grows in the Pacific Northwest to heights of
about 10–15 m (30–50 ft) and has flat, green needles and red berries. However, its bark
contains the miracle drug Taxol, now used to treat ovarian, lung, breast and colon cancer.
The biological action of the yew tree has been known since Greek times, and Native
Americans used the tree for medicinal purposes. Because of this known history, researchers
in the 1960s included the tree in large-scale screening for cancer-fighting agents. The
positive results eventually led researchers to isolate the active ingredient Taxol. But the
amount of Taxol needed to treat a single cancer patient required the harvesting of several
trees that were around 100 years old, creating environmental problems. As often happens
with natural products, however, researchers came up with another way to obtain the
compound: Taxol is now synthesized from a precursor found in the needles of the
European yew tree. Because the trees don’t have to be cut down to harvest the needles, this
route is sustainable. Today, millions of cancer patients have benefitted from this natural
product. The story of Taxol is representative of the field of natural products research, an
active area that produces many novel and useful compounds.
3-SECOND NUCLEUS
Plants, animals and microbes are sources of valuable and often healing chemical compounds.
3-MINUTE VALENCE
Natural products researchers scour living organisms for the useful chemicals they might contain. For
example, penicillin (an antibiotic) was extracted from microbes, and the early form of aspirin was
extracted from the bark of the willow tree. Often chemists later find ways to synthesize these compounds
in the laboratory, but the myriad of compounds in nature often shows us the way.
30-SECOND TEXT
Nivaldo Tro
RELATED TOPICS
See also
BIOTECH DRUG SYNTHESIS
MONROE ELIOT WALL
1916–2002
American chemist credited with the co-discovery of Taxol
MANSUKH C. WANI
1925–
Indian American chemist credited with the co-discovery of Taxol
The yew tree is the source of the cancer-fighting agent Taxol.

POLYMERS
Polymers permeate most of human life. It is hard to imagine society without them, given
the significant role natural and synthetic polymers play – from medicine to food packaging,
and from clothing to housewares. German chemist Hermann Staudinger first demonstrated
the existence of macromolecules (polymers) as large, chain-like molecules of smaller
repeating units called monomers. Humans have known natural polymers, such as cotton
and rubber, for thousands of years. But their chemical structure was long subject to debate
until Staudinger proved the macromolecular structure of natural rubber – a Nobel Prize-
winning discovery in 1953. The term polymer is derived from the Greek poly meros,
meaning many parts. Many molecules can act as monomers, making it possible to create a
wide range of polymeric materials with desired characteristics. Polyethylene, for example –
one of the most common plastic materials found in packaging bags and bottles – is a chain-
like molecule consisting of an ethylene monomer backbone. Polymers can have high
molecular mass as monomers can link in a variety of ways to grow into very large
molecules. Some are light, hard, strong and flexible; others exhibit unique chemical,
thermal, electrical and optical characteristics.
3-SECOND NUCLEUS
Polymers, chain-like macromolecules consisting of chemically linked repeating units (monomers), play an
unmatched role providing convenience in many aspects of human life.
3-MINUTE VALENCE
Polymers are in general known as electrical insulators. However, some organic polymers – consisting of
monomer units linked by alternating single and double bonds in the carbon backbone – exhibit a low,
inherent electrical conductivity, which can significantly be improved by chemically mixing in electron-
donating and/or -receiving agents, a process called doping. Doped polymers, such as organic light
emitting diodes (OLED), have revolutionized the electronics industry.
RELATED TOPICS
See also
HYDROCARBONS
HERMANN STAUDINGER
1881–1965
German chemist who won the 1953 Nobel Prize in Chemistry for discovering the macromolecular
structure of natural rubber
HIDEKI SHIRAKAWA
1936–
Japanese chemist who won the 2000 Nobel Prize in Chemistry for co-discovering the existence of
conductive polymers
30-SECOND TEXT
Ali O. Sezer
Polymers are chain-like molecules that compose a range of substances such as

plastics.
BIOCHEMISTRY
BIOCHEMISTRY
GLOSSARY
acid group A functional group consisting of –COOH.
adenosine triphosphate A biomolecule with the formula C10H16N5O13P3 that is used as a

main vessel for energy transport in living organisms.
alkanes Hydrocarbons with the general formula CnH2n+2.
amine group In an amino acid, the -NH2 group.
amino acids The individual units that, when linked together in a specified order, form
proteins. Amino acids have a central carbon atom, an amine group, an acid group and a
side chain (that varies in structure from one amino acid to another).
base pair The two parts of nucleic acids that uniquely pair together to form the double
helix in DNA and allow precise copying. In DNA, adenine pairs with thymine and guanine
pairs with cytosine.
carboxylic acid group The –COOH group in organic and biochemical compounds. The
group is polar and acidic.
cellulose A complex carbohydrate composed of repeating glucose units. Cellulose is the

main structural material in plants.
DNA Deoxyribonucleic acid, a biomolecule composed of repeating units (called

nucleotides) responsible for carrying the genetic information in all known living
organisms.
disaccharides A class of sugars composed of two monosaccharides linked together.
esters A class of organic compounds consisting of a –COO– group sandwiched between

two or more carbon atoms.
flash photolysis A technique to study light-activated chemical reactions in which a flash of

light is used to initiate the chemical event which is then monitored as a function of time.
genome The complete set of genetic material of an organism.
glucose A carbohydrate with the formula C6H12O6 that circulates in the blood of animals
and humans.
hormones Biochemical compounds that are transported in the blood to targets where they
stimulate and regulate biochemical processes.
modular polymers Polymers that can be built up one unit (or monomer) at a time.
monosaccharides A carbohydrate composed of three to eight carbon atoms and one
aldehyde or ketone group.
nonpolar A substance composed of molecules with uniform charge distribution. Nonpolar

substances generally do not mix well with water.
nucleotide The individual unit that, when linked with other nucleotides, forms a nucleic
acid (such as DNA). Each nucleotide contains a phosphate group, a sugar and a base.
polar A substance composed of molecules with an asymmetric charge distribution.
polynucleotide A chain of nucleotides bonded together found in hereditary molecules such

as DNA and RNA.
recombinant DNA Synthetic DNA that contains genetic material from different sources.
ribonucleotide The monomer that, when linked to other ribonucleotides, forms RNA.
sucrose A carbohydrate with the formula C12H22O11.
triglyceride A type of fat that has a three-carbon backbone with three fatty acids attached
(one to each carbon atom).
CARBOHYDRATES
Carbohydrates are so named because their general formula is a multiple of one carbon atom
and one water molecule, (CH2O)n. Structurally, the carbon atoms are arranged in a ring
(that can interconvert into a straight chain) and have multiple hydroxyl (OH) groups
attached, making simple carbohydrates polar and therefore soluble in water. The ability to
dissolve in water is important to one of the main functions of carbohydrates: storing and
transporting energy for living organisms. The carbohydrate glucose (C6H12O6) is typical. It
must be easily transported in the blood to places in the body where energy is being used.
Carbohydrates such as glucose (which are also called monosaccharides, meaning one
sugar) can link together to form disaccharides, such as sucrose (C12H22O11), which is table
sugar. They can also link together to form long, chain-like molecules called complex
carbohydrates such as starch, glycogen and cellulose. Starch (think potatoes) is the main
energy storage medium for plants, and glycogen is used by animals as a compact way to
store glucose in the muscles. Cellulose is the most common organic substance on Earth. It
is more rigid than the other complex carbohydrates and is the main structural component in
plants.
3-SECOND NUCLEUS
Carbohydrates are multi-carbon aldehydes or ketones with many OH groups attached; they act as short-
term energy stores and the main structural components of plants.
3-MINUTE VALENCE
Carbohydrates are common in the foods we eat. Monosaccharides can pass directly through our intestinal
wall and enter the bloodstream as ready sources of energy. Disaccharides and complex carbohydrates,
however, must be broken down into monosaccharides before they can pass into the bloodstream. Our
bodies can break down sugars and starches, but we lack the enzyme to break down cellulose (also known
as dietary fibre), which is why cellulose passes through the digestive tract, giving bulk to stools and
preventing constipation.
RELATED TOPICS
See also
LIPIDS
ANDREAS MARGGRAF
1709–82
German chemist who first isolated glucose from raisins
EMIL HERMANN FISCHER

1852–1919
German chemist and winner of the 1902 Nobel Prize in Chemistry for his pioneering work on sugars
30-SECOND TEXT
Nivaldo Tro
Carbohydrates include simple sugars such as glucose (top) and complex

carbohydrates such as cellulose (bottom).
LIPIDS
Lipids are the only biomolecule defined by what they are not: lipids are not able to dissolve
in water. This insolubility enables lipids to form thin, oily membranes and to clump
together into oily droplets that serve as high-density stores of metabolic energy. In fact,
many lipids contain a large, burnable hydrocarbon group similar to the alkanes in gasoline.
In fatty acids (a type of lipid), for instance, a long hydrocarbon chain is attached to a single
polar carboxylic acid group. In tryglycerides (another type of lipid) three long hydrocarbon
chains are attached to a short three-carbon head. This highly nonpolar structure causes
tryglycerides to glob together into oily ‘fat’ droplets. Another type of lipid has only two
long hydrocarbon chains attached to a more polar head (a three-carbon unit containing a
phosphate group). The result is a rod-like molecule with a charged water-loving ‘head’ and
oily tail. These form sheets with the tails lined up in oily sheets on the one side and the
‘heads’ all facing to the other. To keep the oily surface of the tails out of water, two sheets
line up to give a bilayer membrane, with the tails on the inside and the heads forming the
water-facing surfaces. These bilayer membranes are the fundamental barriers that
encapsulate living cells.
3-SECOND NUCLEUS
Lipids’ insolubility in water enables them to form extended membranes that enclose biological solutions
and to function as particularly dense stores of metabolic energy.
3-MINUTE VALENCE
Even though they cannot be built up into modular polymers in the same way that other biomolecules can,
lipids perform many varied biological functions. Lipid membranes act as barriers between the insides and
outsides of cells while triglyceride ‘fats’ function as long-term energy stores in plants and animals. Other
lipids called hormones act as biological messengers, being secreted by glands and carried to target cells
where they trigger a physiological response.
RELATED TOPICS
See also
HYDROCARBONS
MICHEL CHEVREUL
1786–1889
French chemist who was a pioneer in studying the chemistry of soaps, fats and oils
CHARLES ERNEST OVERTON

1865–1933
British biologist who first proposed that lipids might act as a cell membrane
30-SECOND TEXT
Stephen Contakes
One of the many functions of lipids is to encapsulate cells by forming a bilayer.

Proteins are chain-like biomolecules that carry out a bewildering array of functions. Some,
like the collagen in your skin, serve as structural supports. Others, like the motor protein
myosin, enable muscles to relax and contract. Others adopt compact ‘globular’ shapes and
can store or transport smaller molecules around, control cellular metabolism by speeding
up particular chemical reactions or even recognize and bind other molecules. Some
proteins, like insulin, act as intercellular signals, while others regulate bodily processes by
chemically modifying other proteins to adjust how they function. Yet proteins are
comprised of only 20 basic building blocks called amino acids, so named because they all
contain a central carbon atom bonded to an amine group and an acid group. The central
carbon is also bonded to a third variable group called a side chain, which may be polar,
nonpolar, small, large, acidic, or basic. Amino acids can string together to form long
polymers whose properties can vary widely based on the exact sequence of these side
chains. Interactions between the side chains at different points along the polymer with each
other and with surrounding water causes the protein to wriggle and fold into specific
shapes, which in turn determine the functions they can perform.
3-SECOND NUCLEUS
Amino acids can be strung together into protein chains that fold into a diverse array of shapes and carry
out many biological functions.
3-MINUTE VALENCE
When you take a breath the oxygen you breathe becomes bound to a protein called haemoglobin in your
red blood cells, which transports the oxygen to your muscles and other tissues where it is used to ‘burn’
fats and carbohydrates in interconnected sequences of protein-catalyzed reactions. These generate the
energy your body needs to move, synthesize other biomolecules and produce the electrical signals
needed for nerve cells to function.
RELATED TOPICS
See also
GERARDUS JOHANNES MULDER
1802–80
Dutch chemist who first described the composition of proteins
JOHN KENDREW & MAX PERUTZ

1917–97 & 1914–2002
British biochemist and Austrian-born molecular biologist who determined the first 3D structures of
proteins
30-SECOND TEXT
Stephen Contakes
Some proteins fold into globular shapes (centre), while others have more
linear structures (bottom).
ANNA J. HARRISON
Anna Jane Harrison was an American chemist

and educator who believed in the importance
of improving science education and increasing
public awareness of science. Born to a family of
farmers in Benton City, Missouri, Harrison took
an interest in chemistry from as early as
elementary school and by high school this had
turned to fascination. She received all her
advanced degrees from the University of
Missouri-Columbia, including two BA degrees
(in chemistry and education) and a PhD in
physical chemistry. After five years of teaching
at the Sophie Newcomb College of Tulane
University in New Orleans, she took a position
as a chemistry professor at Mount Holyoke
College in Massachusetts, where she taught
until her retirement in 1979. She continued to
teach even after her retirement, at the US Naval
Academy in Annapolis, Maryland.
At Mount Holyoke College, Harrison had a
chance to work with renowned chemistry
professor Emma Perry Carr on the
spectroscopic study of molecular structure.
She carried out research using a technique
called flash photolysis to study chemical reactions by monitoring the dissociation and
association of different molecular compounds. Her research activities also included work carried
out with the A. J. Griner Company of Kansas City on field kits for the detection of toxic smoke for
soldiers in the Second World War.
Harrison is perhaps better known today for her skills in science education. She is credited with
helping change the chemistry profession from being a male-dominated profession to one that is
more welcoming of diversity in gender, race and ethnicity. More than 100 years after its
foundation, the American Chemical Society elected Harrison as its first female president in 1978.
Harrison had a natural talent for making complicated concepts clear and comprehensible to her
students. Her approach to education included helping students acquire better knowledge of how
to make good public policy decisions related to science. In the 1970s, Harrison became an
outspoken advocate of improved communication of science to the public, particularly to public
officials. She served on many advisory boards including the National Science Board, and travelled
to different parts of the world sharing her experience in public education of science.
Ali O. Sezer
23 December 1912
Born in Benton City, Missouri
1933
Receives a BA degree in chemistry from the University of Missouri-Columbia
1935
Receives a BA degree in education from the same institution
1937
Receives an MA degree in chemistry, again from the University of Missouri-Columbia
1940
Receives a PhD degree in physical chemistry, once again from the University of Missouri-Columbia
1945
Joins the chemistry department at Mount Holyoke College in Massachusetts
1960
Receives the Citation of the University of Missouri College of Arts and Sciences
1969
Receives the Manufacturing Chemists Association Award in College Chemistry Teaching
1978
Becomes the first female president of the American Chemical Society
1982
Receives the Chemical Education Award from the American Chemical Society
1983
Serves as the president of the American Association for the Advancement of Science
1989
Co-authors a textbook with Edwin S. Weaver entitled Chemistry: A Search to Understand
8 August 1998
Dies in Holyoke, Massachusetts
THE BIOLOGICAL BLUEPRINT: NUCLEIC ACIDS
DNA is a long, chain-like molecule containing units called nucleotides. Each nucleotide
unit contains a negatively charged phosphate group attached to a carbohydrate ring, which
is itself attached to a wedge-like nitrogen-containing group called a base. Bases come in
four varieties, all of which are flat and nonpolar on top and bottom, but have specific
patterns of polar nitrogen, oxygen and hydrogen atoms along their edges. These patterns
allow bases to recognize ‘complementary’ bases, namely those which have the right pattern
of polar groups to interact strongly, giving a base pair. Therefore, when deoxyribonucleic
acids’ sugar-phosphate groups are linked together into long polynucleotide chains, the
bases along the chain can generate another polynucleotide strand with a sequence of bases
complementary to the first. Some base sequences in DNA encode instructions for making
proteins. These, along with nearby base sequences that tell the cell’s machinery when to
make those proteins, make up the units of heredity called genes. However, nucleic acids
aren’t only used to store and transmit genetic information. The cell’s main energy currency,
adenosine triphosphate (ATP), is a ribonucleotide in which the phosphate has been replaced
by a chain of three linked phosphate groups.
3-SECOND NUCLEUS
Nucleic acids form chains of alternating phosphates and carbohydrates with attached wedge-like
nitrogen-containing bases, the sequence of which encodes biological information.
3-MINUTE VALENCE
Life’s information-bearing molecule is deoxyribonucleic acid or DNA. DNA contains within it the chemical
code for protein synthesis and is passed from parent to offspring, which is why you have characteristics
similar to your parents. In 2003, scientists successfully mapped the entire human genome, a chemical
code containing about 3 billion units (base pairs).
RELATED TOPICS
See also
CARBOHYDRATES
OSWALD AVERY
1877–1955
Canadian-born medical researcher who demonstrated that DNA is genetic material
JAMES WATSON & FRANCIS CRICK

1928– & 1916–2004
American and British molecular biologists who determined DNA’s double-helical structure
30-SECOND TEXT
Stephen Contakes
DNA has a double helical structure in which complementary bases connect

along the middle.
BIOTECH DRUG SYNTHESIS
Before 1922, diabetes was fatal. Then a 14-year-old diabetes patient on the verge of death
was given insulin (a protein that regulates blood sugar) derived from animal sources. The
patient recovered – and survived. Soon insulin (harvested mostly from pigs) became
available for widespread use, changing diabetes into a manageable long-term disease.
However, some patients did not tolerate pig insulin very well. In the 1980s a company
called Genentech figured out a way to synthesize human insulin by inserting the gene for
human insulin into the DNA of bacterial cells. When the bacteria reproduced, they copied
the human insulin gene and passed it on to their offspring. Furthermore, as the genetically
modified bacteria synthesized the proteins they needed to survive and reproduce, they also
synthesized human insulin. The insulin was harvested from the bacterial cultures, purified
and administered to diabetics. Today diabetics take human insulin, synthesized in this way.
The DNA instructions for making desired proteins can also be inserted into the DNA of
plants or animals. For example, in 2015 the FDA approved a drug to treat Wolman disease,
a rare but fatal disease caused by a deficiency of an enzyme called LAL. The drug is
harvested from the eggs of chickens that have been genetically modified to produce LAL.
3-SECOND NUCLEUS
Human proteins can be synthesized by inserting the human gene for the desired protein into bacterial,
plant or animal cells. As these cells grow and divide, they synthesize the desired protein.
3-MINUTE VALENCE
Genetic engineering – the process of modifying an organism’s genome for a particular purpose – has been
used, not only to produce life-saving medicines but also to produce animals or plants with desirable
characteristics. Genetic modification of soybeans, tomatoes and rice has resulted in crops with more
resilience and higher nutritional value. In spite of rigorous scientific testing, the controversy surrounding
some of these products has resulted in increased scrutiny of their safety.
RELATED TOPICS
See also
FREDERICK BANTING
1891–1941
Canadian physician who was awarded the 1923 Nobel Prize in Medicine for his discovery of insulin
FREDERICK SANGER
1918–2013
British biochemist who was awarded the Nobel Prize in Chemistry in 1958 for his determination of the
structure of insulin
PAUL BERG
1926–
American biochemist awarded the 1980 Nobel Prize in Chemistry for his work on recombinant DNA
technology
30-SECOND TEXT
Nivaldo Tro
Human insulin is synthesized by the genetic modification of bacteria.

NUCLEAR CHEMISTRY
NUCLEAR CHEMISTRY
GLOSSARY
alpha particle A type of particle given off in one type of radioactive decay. An alpha
particle contains 2 protons and 2 neutrons and is symbolized as .
amu A unit of mass used for subatomic particles. 1 amu = 1.66 x 10-27 kg.
beta particle A type of particle given off in one type of radioactive decay. A beta particle
is an electron and is symbolized as .
chemical reaction A process in which the atoms in one or more substances (the reactants)
rearrange to form different substances (the products).
critical mass In nuclear fission, the minimum mass of fissile material needed to maintain a
self-sustaining nuclear reaction.
Einstein’s equation E=mc2 An equation that relates mass to energy, which means that the
two are interconvertible.
electron A subatomic particle with a negative charge and a mass of 0.00055 amu.
gamma ray A high energy photon given off in one type of radioactive decay and often in
conjunction with other types. A gamma ray is symbolized as .
gene A strand of DNA that codes for a single protein.
isotope An atom that has the same number of protons as another atom, but a different
number of neutrons.
metabolism The process by which living organisms convert certain compounds into the
energy needed to survive and reproduce.
neutron A subatomic particle with no charge and a mass of 1 amu.
nuclear fission A nuclear reaction in which a large nucleus splits into smaller fragments
and releases energy.
plutonium A synthetic chemical element with atomic number 94 used in nuclear

chemistry, especially nuclear power and atomic bombs.
proton A subatomic particle with a positive charge and a mass of 1 amu.
radioactivity The emission of small energetic particles from the nuclei of certain unstable
isotopes.
radiocarbon dating A method of determining the age of previously living material by
measuring the C-14 content in the material.
radiopharmaceutical Pharmaceutical agents that are radioactive and used in the diagnosis
and treatment of disease.
tracers A chemical compound where one or more atoms have been replaced with a
radioactive isotope that allows a scientist to trace where the atom goes in a particular
process.
uranium A radioactive chemical element with atomic number 92 used in nuclear

chemistry, especially nuclear power and atomic bombs.
X-rays A form of electromagnetic radiation with wavelengths slightly longer than gamma
rays and used to image bones and organs.
RADIOACTIVITY
As a scientific poet once wrote ‘Atoms … fly to bits with utmost facility’.
Counterintuitively, some atoms spontaneously fall apart to produce rays and particles that
can penetrate through various materials, including metals and our own bodies. Antoine
Becquerel and Pierre and Marie Curie, working in Paris in the last decade of the nineteenth
century, were the first to recognize this phenomenon in uranium minerals. Madame Curie
called this ‘radioactivity’ (from the Latin radius, meaning ‘ray’) and soon found two
mysterious, previously unknown elements (‘radium’ and ‘polonium’) that emitted more
intense ‘radiation’ than uranium itself. Initially radioactivity was thought to exist in two
types, designated logically enough by Ernest Rutherford as alpha and beta. (Gamma rays
were discovered several years later.) Positively charged alpha particles, soon found to be
energetic helium nuclei, He2+, had less ability to penetrate various substances. Negatively
charged beta particles, soon found to be energetic electrons, were much lighter and able to
penetrate a variety of materials well. Gamma rays, the most penetrating of all, were high-
energy electromagnetic radiation. Most remarkably, it is now clear that certain types of
atoms spontaneously ‘decay’ and spit out tiny charged particles and highly intense
radiation.
3-SECOND NUCLEUS
Some atoms spontaneously ‘decay’, producing alpha and beta particles and gamma rays that can
penetrate through various materials. This is called radioactivity.
3-MINUTE VALENCE
Radioactive elements can be used as ‘tracers’ to follow the pathway of a chemical reaction or monitor
concentrations of elements in research, environmental, agricultural and medical settings. Radioactive
elements are also used to establish the ages of various objects including once-living systems (carbon-14),
early humanoids (potassium-40) and the Moon, Earth and various rocks and minerals (uranium and
thorium isotopes).
RELATED TOPICS
See also
SPLITTING THE ATOM
3-SECOND BIOGRAPHY
WILLIAM RAMSAY
1852–1916
Scottish chemist who wrote the 1902 poem ‘The Death Knell of an Atom’, which contains the following
stanza ‘So the atoms, in turn, we now clearly discern,/Fly to bits with the utmost facility;/ They wend on
their way, and in splitting, display/An absolute lack of stability.’
30-SECOND TEXT
Glen E. Rodgers
When atoms emit radiation they change their identity.

SPLITTING THE ATOM
In 1938 Otto Hahn shot neutrons at uranium atoms and was amazed to discover that they
appeared to split roughly in half. He had discovered nuclear fission, whereby a large
nucleus splits to form two smaller nuclei and several more neutrons. If a ‘critical mass’ of a
sufficiently pure isotope of uranium or plutonium is present, these additional neutrons can
go on to hit other fissionable nuclei and cause a chain reaction which, as calculated using
Einstein’s equation E=mc2, releases inordinate amounts of energy, far in excess of that
obtained from conventional chemical reactions. This energy can be harnessed to create
electricity (nuclear energy) or to create explosions (nuclear bombs). The uranium-based
bomb dropped on Hiroshima, Japan, on August 6, 1945, was called ‘Little Boy’. In this
‘gun-type’ assembly, the critical mass was obtained by firing a uranium ‘bullet’ into a
hollow cylinder of uranium. The plutonium-based bomb dropped on Nagasaki, Japan, on
August 9, 1945, was called ‘Fat Man’. In this implosion-type assembly, the critical mass
was obtained using a lens assembly that fired small bits of plutonium all towards the centre
of the bomb.
3-SECOND NUCLEUS
Firing neutrons into critical masses of fissionable materials splits the atoms apart and produces
additional neutrons; the resulting chain reaction releases large amounts of energy.
3-MINUTE VALENCE
Why don’t atomic nuclei, particularly those containing dozens of positively charged and therefore
mutually repulsive protons, just burst apart? It turns out that some do. Large nuclei of certain types of
atoms of uranium or plutonium atoms act like wobbly drops of liquid tenuously held together by a
nuclear surface tension that can be easily disrupted.
RELATED TOPICS
See also
INSIDE THE ATOM
OTTO HAHN
MARIE CURIE
1867–1934
Polish-born French chemist who developed the theory of radioactivity
OTTO HAHN
1879–1968
German winner of the 1944 Nobel Prize in Chemistry, who discovered nuclear fission
30-SECOND TEXT
Glen E. Rodgers
In nuclear fission, a neutron causes an unstable nucleus to split, releasing

large amounts of energy.
NUCLEAR WEIGHT LOSS
When an atom splits, either in a nuclear power plant or during the detonation of a nuclear
weapon, a tremendous amount of energy is released. Where does all of this energy come
from? The answer lies in Einstein’s remarkably simple equation that relates energy and
matter: E=mc2 – energy equals mass times the speed of light squared. This equation states
that energy and matter are really two different forms of the same thing. In other words, if
energy is being released (created), then matter must disappear. That’s exactly what happens
during nuclear fission. A large nucleus splits into two smaller ones, a little bit of the total
mass is destroyed – and lots of energy is produced. Does this mean one or two protons or
neutrons get vaporized? No, the fascinating part of this is that all of the protons and
neutrons lose a little bit of their mass. However remarkable it may seem, this means that
protons and neutrons do not always have the same mass. A proton in a uranium nucleus
weighs more than a proton in an iron nucleus. After splitting, the same total number of
protons and neutrons exist; they all weigh just a bit less. This is not a recommended weight
loss programme for humans.
3-SECOND NUCLEUS
Protons and neutrons each lose a tiny bit of mass when nuclear fission occurs. This mass is converted into
energy.
3-MINUTE VALENCE
If matter and energy are two sides of the same coin, then is it appropriate to imagine protons and
neutrons as hard spheres? Is it better to think of them as little balls of energy? Because matter and energy
are interconvertible, perhaps it doesn’t really matter. This is another indication that the subatomic
universe is a very strange place.
RELATED TOPICS
See also
INSIDE THE ATOM
RADIOACTIVITY
SPLITTING THE ATOM
LISE MEITNER
1878–1968
Austrian physicist who performed the first mass/energy calculations on nuclear fission
ALBERT EINSTEIN
1879–1955
German-born physicist who provided mathematical equivalence to mass and energy
30-SECOND TEXT
Jeff C. Bryan
When an atom splits through nuclear fission, some of its mass is converted into
energy.
THE EFFECT OF RADIATION ON LIFE
The types of radiation discussed in this chapter are rather unusual in that they have the
power to knock electrons loose from atoms and molecules. As the radiation travels through
matter, it transfers some of its energy to the molecules it passes by, much like a bullet fired
into a pile of pea gravel. Since electrons bind atoms together in molecules, this subatomic
violence can lead to broken chemical bonds. If enough radiation damage occurs in a single
cell, a large number of molecules get broken and the cell could die. If it’s less damaged, it
can repair itself. However, if the cell’s DNA is damaged, the cell could change (or mutate)
in ways that cause it to grow abnormally (because DNA directs how cells grow). These
mutations and abnormal cell growth can lead to cancer. This sounds bad, especially since
humans, like all living things and the planet, are naturally radioactive. Fortunately, we’ve
evolved with rather efficient cell repair mechanisms. It appears that below a certain
threshold, radiation produces no negative health effects. Some set this threshold at 100
mSv (millisieverts, a unit of dose). For reference, the global average annual dose for
natural and anthropogenic radiation is 2.8 mSv.
3-SECOND NUCLEUS
Radiation can break chemical bonds in living things, possibly leading to cell death or cancer.
3-MINUTE VALENCE
Radiation damage to DNA typically takes place indirectly. The most common chemical in living things is
water, making it the odds-on favourite to have one of its electrons knocked loose. This forms H2O+, which
falls apart into H+ and HO·. HO· is known as hydroxyl radical, and is very reactive. If it bumps into a DNA
molecule, it will likely disrupt a chemical bond in the DNA.
RELATED TOPICS
See also
HERMANN J. MÜLLER
1890–1967
American biologist and winner of the 1946 Nobel Prize in Medicine who first observed changes in genes
after exposure to X-rays
L. HAROLD GRAY
1905–65
English physicist and radiobiologist who pioneered studies of radiation effects on living things
30-SECOND TEXT
Jeff C. Bryan
DNA can be damaged by ionizing radiation.

OTTO HAHN
Otto Hahn was often ill as a child, managing to survive

both diphtheria and severe pneumonia. He never
regarded himself as a good student, but both his health
and grades improved dramatically in his early teens. At
about the same time, he and a friend started performing
simple chemical reactions with materials they could find
around the house. This interest intensified when he took
an evening course on the chemistry of dyes. He went on
to study chemistry at the universities of Marburg and
Munich.
After earning his PhD, and a year of military service,
Hahn returned to Marburg for a position assisting with
lectures. Hahn was interested in working in Germany’s
chemical industry, and learned of a position that
involved international travel. His potential employer
wanted Hahn to spend some time in England before they
would consider him, so Hahn’s advisor arranged for him
to work with William Ramsay in London.
Ramsay gave Hahn a couple of radioactivity puzzles to
research, and, although they were outside of Hahn’s area
of expertise (organic chemistry), he excelled in solving
both. Ramsay was so impressed that he convinced Hahn he should pursue an academic career in
nuclear science. Hahn was interested, but felt he needed more depth in this new field. After a year
in London, he went to Montreal to spend a year working with Ernest Rutherford.
Ramsay then helped Hahn get a position at the University of Berlin; arriving shortly after Hahn,
was Austrian physicist Lise Meitner. Hahn and Meitner worked together for more than 30 years
and were immensely productive in identifying many of the decay products of uranium and
thorium, including the element protactinium. Meitner had to leave Germany in 1938, and shortly
after that Hahn, working with Fritz Strassmann, observed nuclear fission. They didn’t understand
what they were seeing, so they wrote to Meitner about it. Meitner and her nephew Otto Frisch
figured out it was nuclear fission. Hahn and Strassmann published their observations in January
1939, and Meitner and Frisch their interpretation a month later.
This discovery shook the scientific community, and eventually led to the Manhattan Project
(the research project in the United States that produced the first nuclear weapons) as well as the
development of nuclear power plants. During the Second World War, Hahn continued his work
identifying the many products of fission. After the war, he discontinued his research and served as
president of the Max Planck Society until 1960.
Jeff C. Bryan
8 March 1879
Born in Frankfurt, Germany
1901
Earns a doctorate in organic chemistry at the University of Marburg
1904–5
Works with William Ramsay at University College, London
1905–6
Works with Ernest Rutherford at McGill University in Montreal, Canada
1907
Qualifies as a university lecturer at the University of Berlin
1914–18
Serves as a chemical warfare specialist in the German army
1918
Discovers protactinium and nuclear isomerism with Lise Meitner
1928
Appointed director of the Kaiser Wilhelm Institute
1938
Observes nuclear fission, with Fritz Strassmann
1944
Awarded the Nobel Prize in Chemistry for the discovery of fission
1966
Shares the Enrico Fermi Award with Lise Meitner and Fritz Strassmann for the discovery of fission
28 July 1968
Dies in Göttingen, West Germany
NUCLEAR MEDICINE
Nuclear medicine involves the injection of a radioactive material (a radiopharmaceutical)

into a patient to diagnose or treat a disease. An example is 18F-fluorodeoxyglucose (FDG),
a radioactive sugar molecule. In our bodies, sugars tend to go to sites of metabolism. They
also collect in cancerous tumours, because cancer is a sugar hog. Once the
radiopharmaceutical is allowed to localize, radiation detectors can be positioned around the
patient to generate three-dimensional images of the organs where the radiopharmaceutical
has accumulated. The data collected from a nuclear medicine scan typically tells us more
about how well the organ is functioning (physiology) than what it looks like (anatomy). By
changing the chemical nature (size, shape, charge) of the radiopharmaceutical, we can
obtain images from any organ in the body and determine how well it’s working. Nuclear
medicine scans make patients more radioactive. But remember that we are all naturally
radioactive; nuclear medicine simply adds more that concentrates in part of the body. The
radiation dose is typically low enough not to have any measurable adverse effects, and the
benefits of diagnosing or treating a disease you already have outweighs any nearly
negligible risk that the radiation might pose.
3-SECOND NUCLEUS
Nuclear medicine uses radiopharmaceuticals to examine physiology and to treat diseases.
3-MINUTE VALENCE
As we gain a better understanding of human physiology, radiopharmaceuticals are becoming so
sophisticated they can generate images and perform therapy at the cellular and molecular level. Imagine
being able to kill cancer when it is so small that it can’t even be located by conventional means. We may
soon be able to detect and treat cancer before any outward symptoms are apparent.
RELATED TOPICS
See also
RADIOACTIVITY
GEORGE DE HEVESY
1885–1966
Hungarian-born winner of the 1943 Nobel Prize in Chemistry who first recognized that radioactive
isotopes could be used to study complex chemical processes such as metabolism
HAL ANGER
1920–2005
American electrical engineer and biophysicist who invented the cameras that are still widely used in
nuclear medicine
30-SECOND TEXT
Jeff C. Bryan
Radioactive substances can be used to image internal organs.

ENJOYMENT OF WINE
RESOURCES
BOOKS
Cathedrals of Science: The Personalities and Rivalries that Made Modern Chemistry
Patrick Coffey
(Oxford University Press, 2008)
Chemistry: A Molecular Approach
Nivaldo J. Tro
(Pearson, ed. 4, 2017)
Chemistry in Focus: A Molecular View of our World
Nivaldo J. Tro
(Cengage, ed. 6, 2016)
Chemistry: Structure and Properties
Nivaldo J. Tro
The Disappearing Spoon: And Other True Tales of Madness, Love, and the History of the World from the
Periodic Table of the Elements
Sam Kean
(Little, Brown and Co, 2010)
The Elements: A Visual Exploration of Every Known Atom in the Universe
Theodore Gray
(Black Dog and Leventhal, 2009)
Inorganic Chemistry
Gary Miessler, Paul Fischer and Donald Tarr
Napoleon’s Buttons: 17 Molecules that Changed History
Penny Le Couteur and Jay Burreson
(Penguin, 2003)
Organic Chemistry
Paula Yurkanis Bruice
The Periodic Table: Its Story and Its Significance
Eric Scerri
(Oxford University Press, 2007)
Physical Chemistry
Peter Atkins and Julio de Paula
(Oxford University Press, ed. 9, 2010)
Stuff Matters
Mark Miodownik (Penguin, 2013)
Uncle Tungsten: Memories of a Chemical Boyhood
Oliver Sacks
(Alfred A. Knopf, 2001)
WEBSITES
Mark Winter, WebElementsTM, https://www.webelements.com/
Nobelprize.org, All Nobel Prizes in Chemistry, https://www.nobelprize.org/nobel_prizes/chemistry/laureates/
NOTES ON CONTRIBUTORS
EDITOR
Nivaldo Tro is a Professor of Chemistry at Westmont College in Santa Barbara, California. He received
his B.S. in Chemistry from Westmont College and his Ph.D. in Chemistry from Stanford University. He
then went on to the University of California at Berkeley, where he did postdoctoral research on ultrafast
reaction dynamics in solution. Professor Tro has authored over 20 journal articles and has been awarded
grants from the American Chemical Society, the Petroleum Research Fund, Research Corporation, and
the National Science Foundation to study the dynamics of various processes occurring in thin adlayer
films adsorbed on dielectric surfaces. He has been honoured as Westmont’s outstanding teacher of the
year three times and has also received the college’s outstanding researcher of the year award. Professor
Tro is best known for his chemistry textbooks, which are used at more than 600 colleges and
universities around the world. About one third of all college students taking chemistry today use a
textbook written by Professor Tro.
CONTRIBUTORS
Jeff C. Bryan earned an A.B. in Chemistry from the University of California, Berkeley and a Ph.D. in
Chemistry from the University of Washington. He is a Professor in the Chemistry faculty of the
University of Wisconsin–La Crosse, where he teaches nuclear and general chemistry courses, and his
scholarship focuses on making nuclear science more accessible to students with limited science and
maths backgrounds. He has written a textbook titled Introduction to Nuclear Science, and co-authored a
lab manual titled Experiments in Nuclear Science.
Stephen Contakes is Associate Professor of Chemistry at Westmont College in Santa Barbara,
California, where he teaches courses in inorganic, analytical, and physical chemistry. With a
background in synthetic organometallic and bioinorganic chemistry, his research interests involve the
preparation of redox-active hydrogen bonded assemblies and photoactive nanoparticle catalysts for use
in pollutant remediation.
Dr. Glen E. Rodgers is a Professor emeritus of Chemistry at Allegheny College in Meadville,
Pennsylvania. Educated at Tufts University and Cornell University, he taught for five years at
Muskingum College in Ohio and 30 years at Allegheny. He taught introductory chemistry on several
levels, plus inorganic chemistry, and numerous interdisciplinary courses with colleagues in other
faculties. He is the author of the third edition (2012) of the popular sophomore-level textbook
Descriptive Inorganic, Coordination, and Solid-State Chemistry (Cengage Learning, International
Edition 2011). Dr. Rodgers and his wife have led science travel tours around the world, taking students
to key locations in the history of science.
Ali O. Sezer is a Professor of Physical Chemistry at California University of Pennsylvania. After
graduating from Yildiz Technical University in Istanbul, Turkey, Sezer went to the U.S.A. to pursue an
advanced degree in chemical and materials engineering. Dr. Sezer’s research interests are in the area of
conducting polymers; particularly nano composites of these polymers with transition metal oxides for
electronics, optical, medical, bio-sensing and corrosion protection applications. He believes in ‘hands-
on’ undergraduate teaching, especially involving students in cutting edge research activities.
James M. Tour is a Professor of Chemistry, Professor of Computer Science and Professor of Materials
Science and NanoEngineering at Rice University in Texas. Tour’s scientific research areas include
nanoelectronics, graphene electronics, green carbon research for enhanced oil recovery and
environmentally friendly oil and gas extraction, carbon supercapacitors and synthesis of single-
molecule nanomachines which includes molecular motors and nanocars. He has also developed
strategies for retarding chemical terrorist attacks. For pre-college education, Tour developed the
NanoKids concept for K–12 education in nanoscale science. Tour has over 600 research publications
and over 120 patents.
Dr. John B. Vincent received a B.S. in Chemistry and Mathematics from Murray State University and
a Ph.D. in Chemistry from Indiana University. He was a NIH postdoctoral fellow at The University of
Virginia before joining the faculty of The University of Alabama, where he is currently Professor of
Chemistry. His research interests are in bioinorganic chemistry, with a particular focus on the nutritional
biochemistry of chromium(III). Dr. Vincent is author or coauthor of over 130 peer-reviewed
publications, over 15 book chapters, 8 books, and 9 patents. Dr. Vincent is currently co-editor-in-chief
of Biological Trace Element Research.
INDEX
A
acids 64, 102, 112, 122, 128, 132
acohol 36, 108, 110
adehyde 102, 110
akali metals 12
akaloids 112
alotrope 84, 96
auminium 86, 114, 115
amines 102, 112
amino acids 128
antacid 64
antibiotics 116
antimony 86
arsenic 86
atomic number 12, 18, 26
atomic theory 12, 14, 30, 31
atomic weights 31
atoms 6, 7, 9, 12, 13, 14, 16, 18, 20, 22, 24, 28, 31, 32, 34, 36, 40, 42, 44, 51, 52, 60,
66, 78, 84, 86, 88, 90, 98, 102, 108, 118, 138, 142, 146
B
barium 72, 73
bases 64, 102, 112, 132
batteries 68, 72, 76
big bang, the 20
blood 8, 108, 110, 124, 128, 134
bonds, bonding 7, 9, 12, 13, 14, 24, 28, 32, 34, 36, 40, 41, 42, 52, 84, 85, 86, 90, 92,
102, 103, 106, 108, 110, 112, 118, 128, 146
covalent bonds and bonding 12, 28, 40, 42, 52, 102, 106
crystal field theory 84
ionic bonds and bonding 12, 28, 40, 42, 52
polar bond 36, 41, 108, 124
valence bond 34, 85
boron 86
Boyle, Robert 44, 50, 60
Boyle’s law 44, 50
Sceptical Chymist (1661) 50, 51
brain 8, 88
C
calcium 72, 73, 90
calcium chloride 54
cancer 8, 9, 116, 146, 150
carbohydrates 124, 132
carbon 20, 86, 96, 102, 106, 108, 110, 112, 118, 124
fullerenes 84, 96
graphene 84
carbon dioxide 60, 62, 86
carbon monoxide 90
carboxylic acid 102, 112, 122
cars 60, 68, 70, 74
nanocars 98
catalyst 58, 70, 84, 92, 96
catalytic cycle 92
cell growth 146
cellulose 124
centromere 40
cesium 12
CFCs 84, 94, 95
chemical reactions 9, 31, 92, 138
chloride 66, 90
chlorine 28, 86, 90, 95
chromium 92
chromosome 40, 41
Clausius, Rudolf 74, 76
coal 62, 106
coal miner’s safety lamp 72, 73
cobalt 92
codeine 112
collagen 128
colour 30, 31, 84, 85, 88
colour wheel 84
complementary colours 84
compounds 7, 9, 28
crystal 40, 52, 78
crystalline structure 40, 48
crystal field theory 84
Curie, Marie 140, 142
Curie, Pierre 140
D
Dalton, John 14, 30
Davy, Humphry 72, 92
diabetes 134
diamond 42, 96
dipole force 40, 42
disaccharide 124
dispersion force 40, 42
DNA 8, 122, 132, 146
E
Earth 26, 62, 86, 90, 95, 104, 140
Einstein, Albert 138, 142, 144
E=mc2 138, 142, 144
electricity 68, 84, 98
electrolysis 73
electrolyte 58
electromagnetism 44
electron 12, 16, 18, 22, 24, 28, 32, 34, 36, 42, 68, 85, 88, 90, 92, 138, 146
electron cloud 13
electronics 96
elements 7, 12, 18, 20, 26, 31, 36, 51, 86, 96, 140
energy 74, 76, 92, 96, 106, 124, 126
entropy 58, 76, 78, 80
enzyme 58, 134
ester 102, 110, 122
F
Faraday, Michael 68, 72, 73
fluorine 86
fossil fuels 62, 98, 106
coal 62, 106
gasoline 106
paraffin wax 106
G
gases 8, 9, 31, 36, 41, 42, 44, 70, 102, 106
genes 132
genetic engineering 134
genome, genomic instability 40, 122, 132, 134
germanium 86
Gmelin, Leopold 110, 115
gold 16
graphene 8, 84, 96
graphite 96
greenhouse gas 62
CFCs 84, 94, 95
H
haemoglobin 128
Hahn, Otto 142, 148
Harrison, Anna J. 130
heat 80
Heisenberg, Werner 22
Heisenberg’s Uncertainty Principle 12, 22
helium 13, 18, 20, 86, 140
Hooke, Robert 50, 51
hydrocarbon 62, 106, 126
hydrochloric acid 64
hydrogen 20, 28, 32, 36, 64, 86, 98, 103, 106, 132
hydroxide 64
I
insulin 128, 134
ions 6, 12, 28, 42, 64, 66, 84, 85, 90
iron 20, 80, 90, 92, 144
iron oxide 80
isomerism 103, 115
isotope 12, 18, 138, 142
K
kelvin scale 74, 78
ketones 103, 110
kinetic energy 44, 58, 74
kinetic molecular theory 44
kinetochore 40
krypton 13
L
Lavoisier, Antoine 60, 62, 72
lead 68, 86
Lewis, Gilbert N. 32
Lewis model 32, 34
ligands 84, 88, 92
light 84, 88, 92
‘like dissolves like’ principle 41, 54
liquids 9, 36, 42, 44, 46
lithium 12
M
magnesium 68, 72, 73
magnet 34, 36, 42
Manhattan Project 149
mass number 12, 18
mass of the atom 12, 18, 31
matter particulate model 6, 7
Meitner, Lise 144, 148, 149
metals 13, 26, 90
alkali metals 26
molecular compound 12
molecules 6, 7, 8, 9, 28, 31, 34, 36, 42, 44, 46, 51, 62, 66, 70, 78, 80, 84, 85, 90, 92,
98, 102, 118, 131, 132, 146
Molina, Mario 94
monosaccharides 122, 124
morphine 112
myosin 128
N
negative charge 12, 16, 28, 36, 40, 42, 85, 132, 138, 140
neon 13
neutralization 64
neutrons 12, 13, 16, 18, 138, 142, 144
nicotine 112
nitrogen 70, 86, 102, 103, 112, 132
nitrous oxide 72
Nobel Prize
in Chemistry
1901 van’t Hoff, Jacobus Henricus 70
1902 Emil Hermann Fischer 124
1913 Alfred Werner 88
1920 Walther Hermann Nernst 78
1943 George de Hevesy 150
1944 Otto Hahn 142, 148
1953 Hermann Staudinger 118
1954 Linus Pauling 48, 66
1958 Frederick Sanger 134
1980 Paul Berg 134
1983 Henry Taube 70
1995 Mario J. Molina 94, 95
1996 Harry Kroto, Richard Smalley 96, 98
2000 Hideki Shirakawa 118
in Medicine
1923 Frederick Banting 134
1946 Hermann J. Muller 146
Peace Prize
1962 Linus Pauling 66
in Physics
1915 Bragg, William Lawrence 48
1926 Jean Perrin 14
1965 Richard Feynman 98
noble gases 13, 26
nonpolar 36, 41, 122, 126, 128, 132
nuclear bomb 142, 144, 149
nuclear fission 138, 142, 144, 148, 149
nuclear fusion 13, 20
nuclear model 13, 16
nucleic acids 132
nucleosynthesis 13, 20
nuclei 13, 16, 18, 22, 24, 140, 142, 144
O
orbital theory 34
osmotic pressure 41
oxidation 68, 84
oxides 58, 62, 64, 70, 73, 80
oxygen 20, 28, 32, 34, 36, 60, 62, 70, 80, 86, 90, 92, 98, 103, 110, 128, 132
P
particle 7, 9, 12, 13, 14, 16, 18, 20, 22, 31, 42, 44, 54
Pauling, Linus 28, 34, 36, 48, 66
penicillin 116
periodic table 18, 19, 26, 27, 86, 87
phosphorus 51, 86
photosynthesis 90
plastics 48, 92, 95, 110
platinum 92
plutonium 142
polar
bond 36, 41, 108, 124
molecule 36, 40, 41, 123, 128, 132
solute 41, 54
pollution 70
polonium 140
polymers 102, 106, 118, 122, 126, 128
porcelain 52
positive charge 13, 16, 28, 36, 40, 42, 138, 140, 142
potassium 12, 72, 73
potential energy 58, 62, 74, 106
precipitation 66
probability 22, 24
progesterone 110
proteins 90, 122, 128, 132, 134
proton 12, 13, 16, 18, 138, 142, 144
Q
quantum mechanics 13, 22, 24, 34
R
radioactivity 13, 140
radium 140
radon 13
Ramsay, William 140, 148, 149
redox reactions 68
reduction 68
Royal Society 30, 50, 114
rubber 118
rubidium 12
Rutherford, Ernest 16, 140, 148 149
S
salt 28, 42, 48, 54, 104
Schrödinger, Erwin 13, 22, 24
Schrödinger’s Cat thought experiment 13, 22
selenium 86
silicon 52, 86
silver 66
sodium 12, 18, 28, 72, 73
sodium chloride 54
sodium chlorine 28
solids 9, 26, 40, 42, 44, 48, 66
solution 54, 66
stars 20, 96
Strassmann, Fritz 148, 149
sugars 28, 104, 124, 150
artificial sweeteners 108
glucose 124
sucrose 124
sulfur 86, 90, 103
Sun 22, 24, 95
sunlight 90, 98
supernova 20
T
tellurium 86
telomere 41
testosterone 110
thermodynamics
first law 74
second law 76, 80
third law 78
thorium 140
tin 86
transition metals 58, 70, 84, 88, 90, 92
U
uranium 20, 140, 142, 144
urea 104, 114, 115
V
vacuum 51
valence electrons 13, 32, 85, 86
valence bond 34
van der Waals, Johannes Diderik
36, 42
velocity 13, 22
Volta, Alessandro 726, 48, 52, 54, 60, 62, 64, 66
W
water, (also ice) 14, 28, 32, 36, 42, 4, 78, 80, 90, 98, 108, 124, 126, 128, 146
Wöhler, Frederich 104, 114
X
X-rays 96, 146
xenon 13
Z
zinc 68
Zintl ions 85
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30-SECOND

Atoms, Molecules & Compounds

Chemical Reactions & Energetics

A tour of this book

classical physics Physics before the advent of quantum mechanics.

Heisenberg’s Uncertainty Principle The quantum mechanical principle that certain

molecular compound A compound, usually composed of two or more non-metals, that

neutron A subatomic particle with no charge and a mass of 1 amu.

nucleosynthesis The process by which elements form within stars.

proton A subatomic particle with a positive charge and a mass of 1 amu.

Schrödinger’s Cat thought experiment A thought experiment involving the application

velocity A measure of how fast (and in what direction) an object is moving.

Mendeleev formulated one of the first periodic tables, which organizes

Water is a molecular compound, composed of two hydrogen atoms bonded to

John Dalton was born into a poor, staunchly

Molecular orbital theory predicts that oxygen should be a magnetic liquid,

A polar molecule has an asymmetrical charge distribution that causes an

crystalline solid A solid whose atoms or molecules are arranged in a well-ordered,

macroscopic properties of gases Properties such as temperature, volume, pressure and

polar bond A chemical bond with asymmetric charge distribution.

polar solute A solute (component of a solution) that has an asymmetric charge

single liquid phase A liquid mixture with uniform composition.

solute The minority component of a solution.

the 30-second chemistry

The strength of the intermolecular forces between water molecules in ice

the 30-second chemistry

the 30-second chemistry

the 30-second chemistry

Robert Boyle, born in a castle in Lismore,

the 30-second chemistry

the 30-second chemistry

electrolyte A substance that produces an electrically conductive solution when dissolved in

entropy A thermodynamic quantity related to the amount of energy dispersed into a

exothermic A reaction that emits energy into the surroundings.

filtration A process of separation in which a solid is separated from a liquid using a

hydrocarbon An organic compound containing only carbon and hydrogen.

oxide An oxygen-containing compound.

transition-metal oxides Compounds containing a transition metal and oxygen.

WALTHER HERMANN NERNST

Batteries use chemical reactions that involve the transfer of electrons to

Controlling how fast a chemical reaction occurs allows us to reduce pollution

Humphry Davy, ‘full of mischief, with a

A perpetual motion machine cannot exist according to the second law of

LUDWIG EDUARD BOLTZMANN

CFCs Chlorofluorocarbons. These compounds were common in air conditioning and

complementary colours Two colours opposite each other on a colour wheel.

complex (transition metal complex) A compound or ion consisting of a transition metal

electromagnetic spectrum The range of frequencies of electromagnetic radiation bounded

substrate The molecule on which an enzyme (a biological catalyst) acts.

Zintl ions Ionic clusters of main group elements.

JOHN HASBROUCK VAN VLECK

Cluster compounds have polyhedral shapes and unique properties.

Many industrial chemicals are produced by combining small organic molecules or

KARL ZIEGLER & GIULIO NATTA

Transition metal compounds can act as catalysts in chemical reactions.

Born to a Mexican family of highly educated

aldehydes A family of organic compounds containing a terminal C=O functional group.

aldosterone A hormone responsible for the regulation of sodium and potassium.

alkaloids Organic bases found in plants; often poisonous.