Lecture-3-Chemical Bonds and Functional Groups
Lecture-3-Chemical Bonds and Functional Groups
Lecture-3-Chemical Bonds and Functional Groups
BIO 111
Mr. Derrick Banda MSc, BSc
LECTURE 3:CHEMICAL BONDS AND
FUNCTIONAL GROUPS IN BIOMOLECULES
Introduction to Chemical Bonds
• Chemical Bonding refers to connections between two or more atoms,
molecules, or ions to give rise to a chemical compound.
• These chemical bonds are what keep the atoms together in the
resulting compound.
• Only the electrons present in the outer shell, also known as the valence electrons take part in
the formation of chemical bonds.
• Generally, the valency of an element is either equal to the number of dots in the corresponding
Lewis symbol or 8 minus the number of dots (or valence electrons).
Types of Chemical Bonds
• The type of chemical bonds formed vary in strength and properties.
• There are 4 primary types of chemical bonds which are formed by
atoms or molecules to yield compounds. These types of chemical
bonds include:
1. Ionic Bonds
2. Covalent Bonds
3. Hydrogen Bonds
4. Van der waals interaction
• These types of bonds in chemical bonding are formed from the loss,
gain, or sharing of electrons between two atoms/molecules.
Types of Chemical Bonds
• The type of chemical bonds formed vary in strength and properties.
• There are different types of chemical bonding possible between atoms
which make the molecules. Types of bonding that are considered to
exist in molecules are categorized as shown below.
• These types of bonds in chemical bonding are formed from the loss,
gain, or sharing of electrons between two atoms or molecules.
Introduction to Chemical Bonds
• Valance electrons are the electrons that form the outermost
shell of an atom.
Introduction to Chemical Bonds
• A common atom contains a nucleus composed of protons
and neutrons, with electrons in certain energy levels
revolving around the nucleus.
• The other atom develops a positive charge and is called the cation. The ionic
bond gains strength from the difference in charge between the two atoms,
i.e. the greater the charge disparity between the cation and the anion, the
stronger the ionic bond.
Formation of Sodium Chloride (NaCl)
• The atomic number of Sodium is 11 and its electronic configuration is 2, 8, 1. It has one
electron excess to the nearest stable electronic configuration of a noble gas - Neon. So sodium
has a tendency to lose one electron from its outermost shell and acquire a stable electronic
configuration forming sodium cation (Na+).
• Electron atomic number of chlorine is 17 and its electronic configuration is 2, 8, 7. It has one
electron less to the nearest stable electronic configuration of a noble gas - Argon. So chlorine
has a tendency to gain one electron to acquire a stable electronic configuration forming
chloride anion (Cl−).
• When an atom of sodium combines with an atom of chlorine, an electron is transferred from
sodium atom to chlorine atom forming sodium chloride molecule thus both the atoms achieve
stable octet electronic configuration.
Formation of Magnesium Chloride (MgCl2)
• The atomic number of Magnesium is 12 and the electronic configuration is 2,
8, 2. It has two electron excess to the nearest stable electronic configuration
of a noble gas - Neon. So magnesium has a tendency to lose two electrons
from its outermost shell and acquire a stable electronic configuration forming
magnesium cation (Mg2+).
• As explained earlier two chlorine atoms will gain two electrons lost by the
magnesium atom forming magnesium chloride molecule (MgCl2)
Covalent Bonds
• A covalent bond indicates the sharing of electrons between atoms.
Compounds that contain carbon (also called organic compounds)
commonly exhibit this type of chemical bonding.
• The pair of electrons which are shared by the two atoms now extend
around the nuclei of atoms, leading to the creation of a molecule.
Single and multiple Covalent Bonds
• The number of pairs of electrons shared between two atoms
determines the type of the covalent bond formed between them.
• When more than one pair of electrons are shared between atoms
multiple covalent bonds form. These can be double or triple
bonds depending on the number of pairs of electrons shared
Formation of single bond in hydrogen (H2) molecule
• Hydrogen molecule is formed by two hydrogen atoms. Each having one
valence electron (1s1), it is contributed to the shared pair and both
atoms acquire stable completely filled electronic configuration.
• The double covalent bond that occurs between the two carbon atoms
in ethane can also be represented by a structural formula and with a
molecular model as shown above.
Formation of triple bond in nitrogen (N2) molecule
• Nitrogen molecule is formed by two nitrogen atoms. Each nitrogen
atom has five valence electrons (2, 5). These two atoms achieve a stable
completely filled electronic configuration (octet) by sharing three pair
of electrons. Hence a triple bond is formed in between the two atoms.
Polarity and Covalent Bonds
• Covalent bonds can be either be Polar or Non-Polar in nature.
• Polarity is the competing forces between two atoms for the electrons.
• The more strongly an atom attracts the electrons in its bonds, the larger its
electronegativity.
• Metals on left side of periodic table attract electrons weakly, thus lower EN.
• Halogens and other reactive nonmetals on right side of periodic table
attract electrons strongly, higher electronegativities
Electronegativity and Bond Polarity
• One way to figure out what type of bond a molecule has is by determining
the difference of the electronegativity values of the molecules.
• This occurs when the electronegativities of the two atoms are not equal,
causing the more electronegative atom to “steal” the electrons from the
other atom.
Polar Covalent Bonds in Water (H2O) molecule
• In a water molecule (above), the bond connecting the oxygen to each
hydrogen is a polar bond.
• The hydrogen bonds help the proteins and nucleic acids form and
maintain specific shapes.
Hydrophobic and Hydrophilic interactions
• Hydrophobic and hydrophilic interactions are two major
intermolecular forces between hydrophobic nonpolar and hydrophilic
polar sites of macromolecules or materials surfaces in solvents.
• A hydrophobic substance is one that has a weak or no affinity to
water. Examples of hydrophobic substances include oils, fats, and other
greasy substances.
• A hydrophilic substance is one that has a strong affinity toward
water. Examples of hydrophilic substances include sugars, salts, vinegar,
and many amino acids.
• Hydrophobic interactions are relatively stronger than other weak
intermolecular forces (i.e., Van der Waals interactions or Hydrogen
bonds).
Hydrophobic interactions
• Hydrophobic interactions describe the relations between water
and hydrophobes (low water-soluble molecules). Hydrophobes are nonpolar
molecules and usually have a long chain of carbons that do not interact with
water molecules.
• The mixing of fat and water is a good example of this particular interaction.
Biological Importance of Hydrophobic Interactions
• Hydrophobic Interactions are important for the folding of proteins. This is
important in keeping a protein stable and biologically active, because it
allows the protein to decrease in surface area and reduce the undesirable
interactions with water.
• Besides from proteins, there are many other biological substances that rely
on hydrophobic interactions for its survival and functions, like the
phospholipid bilayer membranes in every cell of your body.
Hydrophilic interactions
• A hydrophobic substance is one that has a weak or no affinity to water.
Examples of hydrophobic substances include oils, fats, and other greasy
substances.
• A hydrophilic substance is one that has a strong affinity toward water.
Examples of hydrophilic substances include sugars, salts, vinegar, and
many amino acids.
• The forces are named for the Dutch physicist Johannes Diderik van
der Waals, who in 1873 first postulated these intermolecular forces
in developing a theory to account for the properties of real gases.
• Van der Waals attractions can occur between any two or more
molecules and are dependent on slight fluctuations of the electron
densities, which are not always symmetrical around an atom.
• Therefore, the O-H and O-C bonds in the hydroxyl group will be polar covalent
bonds. The figure above shows the partial charges δ+ and δ- associated with
hydroxyl group.
Importance of Hydroxyl R-OH group
• Alcohols are organic compounds in which the hydroxyl functional
group (-OH) is bound to a carbon atom.
Aldehyde Ketone
• Aldehydes differ from ketones in that the carbonyl is placed at the end
of the carbon skeleton rather than between two carbon atoms of the
backbone.
Ketones RC(=O)R’
• When a carbonyl functional group is placed within a molecule, it is known as
a ketone. Ketones are organic compounds with the structure RC(=O)R’,
where R and R’ can be a variety of carbon-containing substituents.
Carboxyl R-COOH
• Carboxylic acid is a combination of a carbonyl group and a hydroxyl
group attached to the same carbon, resulting in new characteristics.
Structure
• The carboxyl group can ionize, which means it can act as an acid and
release the hydrogen atom from the hydroxyl group as a free proton
(H+).
Carboxylate RCOO-
• A carboxylate ion is the conjugate base of a carboxylic acid.
Structure
• Carboxylate ions are the conjugate bases of carboxylic acids, ie. the
deprotonated carboxylic acid. Carboxylate ions can be shown in text
as: RCOO-.
Carboxylate RCOO-
• A carboxylate ion is the conjugate base of a carboxylic acid.
Phosphate R-PO4
• A phosphate group is an phosphorus atom covalently bound to 4
oxygen atoms and contains one P=O bond and three P-O− bonds.
Structure