ORGANIC CHEMISTRY FORM 3 CHEMISTRY NOTES

ORGANICCHEMISTRY I

Organic chemistry is the study of carbon compounds excluding the oxides of

carbon and carbonates.

Carbon forms a very large number of compounds. This is due to the fact that carbon:

(a)   Uses all its valence electrons to form four covalent bonds with carbon atoms and with
atoms of other elements.

(b)   Can form single, double and triple bonds with other carbon atoms.

(c)   Atoms can join each other to form long chains.

HYDROCARBONS.

Hydrocarbons are compounds which are made up of carbon and hydrogenatoms only.

They are classified into three groups depending on the type of bond that existsbetween
individual carbon atoms in a molecule. The groups are alkanes, alkenes and alkynes.

1. ALKANES
Alkanes are a group of hydrocarbons whose carbon atoms are linked by single covalent
bonds.

Hydrocarbons in which only single covalent bonds are present in the molecules are said to
be saturated.
Sources of Alkanes
Alkanes occur naturally as natural gas, biogas and in crude oil.

Crude oil is the major natural source of alkanes. It contains a range of alkanes which can be
separated into various components by fractional distillation. This is due to the fact that the
different alkanes have different boiling points. The fractions with short carbon chains have
low boiling points. As the boiling point of the fractions increase, the viscosity and the
intensity of colour of the fractions increase while flammability decreases.

Crude oil is separated into different components through fractional distillation. Each
component separates at different temperature at different parts of the fractionating column.
The different fractions have different uses.

Cracking of Alkanes

Long chain alkanes are broken up through a process called cracking of alkanes.

During the cracking process short chain alkanes, alkenes and hydrogen are produced.

The general equation for cracking is:

Long chain alkane Smaller chain alkane + Alkenes + Hydrogen For example, when propane
is irradiated with high energy radiation, the following reaction occurs.

There are two ways of cracking of alkanes; thermal cracking and catalytic cracking.

 Thermal cracking takes place at a very high temperature and only involves heating
the long chain alkanes.
 Catalytic cracking takes place at a relatively low temperature and involves heating
the long chain alkanes in the presence of a catalyst and at low pressure.

Nomenclature
Alkanes have names which end with the suffix, – ane; and a prefix numeral used to indicate
the number of carbon atoms in the chain. The first four members have their prefixes as
meth-, eth-, prop –but– with the next members being , pent- (5), hex- (6), and hept- (7).
The simplest alkane is methane where n = 1 and its formula is CH4.

In the skeletal formula, only bonds between carbon atoms are shown. The bonds are drawn
in a zig-zag manner. A straight section of a zig-zag line represents a covalent bond between
two carbon atoms in the structure.

A molecular formula shows the elements present in a compound and the proportions of their
atoms in the compounds.

A structural formula shows how the atoms of the different elements are arranged in the
compound.

The consecutive members of the alkane homologous series differ by a – CH2 unit, and
conform to the general formula CnH2n+2 where n is 1, 2, 3…

A homologous series is a group of compounds with similar chemical properties, chemical

formulae, and they exhibit a steady gradual change in physical properties.

The homologous series of alkanes has the following characteristics:

(i)    All members conform to a general molecular formula of CnH2n+2.

(ii)   All members show similar chemical properties.

(iii)   The physical properties of the members change gradually along the series.

(iv)  The general methods of preparation can be applied to any member of the series.

Isomerism in Alkanes
Isomersare compounds that have the same molecular formula but different structural
formulae.
The isomers of the same alkane differ in their physical properties such as boiling points,
melting points and density but their chemical reactions are similar.

If any hydrogen atom attached to an alkane chain is removed, an alkyl group is formed. The
suffix –ane in the alkane is replaced by –yl, for example:

Alkane Alkyl group

Methane, CH4 Methyl, CH3–

Ethane, CH3CH3 Ethyl, CH3CH2–

Butane, CH3CH2CH2CH3 Butyl, CH3CH2CH2CH2–

Methane, ethane, and propane  do not have isomers. Isomerism in alkanes starts from
butane.

If any hydrogen atom attached to any middle carbon atom is replaced by an alkyl group, a
branched alkane is obtained.

Rules for naming of the branched alkanes

1. Identify the longest continuous carbon chain to determine the name of the parent
alkane. For example, in the structure,

The longest chain has four carbon atoms hence the parent name is butane.

2. Number the longest chain from the end of the chain that is near the branching. For
example, in the structure above, numbering should start from the left, thus:

The branching is therefore on carbon 2 of the longest chain and the substituent group is a
methyl.

3. In case there are two or more similar substituent groups in the chain, they are
indicated by the prefixes; di-, tri-, tetra-, … Comas are used to separate the
numbers for example, in the following:
There are two methyl groups attached to carbon number two of the longest chain hence, 2,
2 -dimethyl. When naming the Isomers of an alkane, the position of the substituent group is
written first followed by the name of the substituent group and finally the name of the
parent alkane. 

Examples

4. When the substituent groups are a halogen and an alkyl group, the halogen is
always placed before the alkyl group. For example;

Preparation of Alkanes
In the laboratory, alkanes are prepared by the reaction between sodalime (mixture of
sodium hydroxide and calcium oxide) and an appropriate alkanoate.

When a mixture of sodium ethanoate and soda lime (sodium hydroxide and calcium oxide) is
heated, methane gas is obtained.

Similarly, when a mixture of sodium propanoate, and soda lime is heated ethane gas is
obtained.

Physical Properties
 Methane is a non-poisonous, colourless gas.
 It is slightly soluble in water and hence can be collected over water. However, it is
quite soluble in organic solvents such as ethanol and tetrachloromethane. It is less
dense than air.

The general physical properties of the first ten alkanes

  The melting and boiling points of alkanes increase with increase in the number
of carbon atoms. An increase in number of carbon atoms results in an increase in
the strength of intermolecular (van der Waals forces).
 The first four straight chain alkanes are gases, the next six are liquids, and the rest
are solids. Density increases with an increase in molecular mass.
 Generally, the solubility of alkanes decreases as the molecular size increases.

Chemical Properties

Combustion

Methane burns in excess air with a pale blue flame to form carbon(IV) oxide and water.

CH4g)+ 2O2(g) → CO2(g) + 2H2O(l)

In a limited supply of air the flame is luminous due to incomplete combustion.

CH4(g) + O2(g) → CO(g) + 2H2O(l)

Other alkanes behave in a similar manner.

Substitution reactions

A substitution reaction is a reaction in which one atom or group of atoms in a

molecule is replaced by another.

Alkanes undergo substitution reactions with halogens in the presence of sunlight because
the halogen molecules are supplied with energy from light necessary to split them into
atoms. These free halogen atoms are very reactive hence they replace the hydrogen atoms
in the methane molecule.

All the alkanes undergo substitution with chlorine and bromine in the presence of sunlight.
When a substituent, like a halogen, is present in the alkane, the resulting
name must contain the halogen. The name of the halogen becomes the prefix, and the
parent alkane, the suffix. The name of the halogen is therefore written as:

Iodo– to represent iodine.

Bromo– to represent bromine.

Chloro– to represent chlorine.

Fluoro– to represent fluorine.

Chlorine reacts with methane in the presence of ultra violet light. Chlorine atoms repeatedly
substitute the hydrogen atoms in the methane molecule until all the hydrogen atoms have
been replaced as shown below.

If bromine is used, it likewise substitutes hydrogen but the reaction is slow. The mixture of
bromine and methane gets decolourised when left in sunlight. The equation for the reaction
of methane and bromine is:

CH4(g) + Br2(g) → CH3 Br(g) + HBr.

Uses of Alkanes
1. Gaseous alkanes such as methane, propane, butane are used in homes as fuels.
2. They are used in the manufacture of carbon black which is a component of printers’
ink, and paint.
3. They are used in the manufacture of methanol, methanal, and chloromethane
which are useful industrial chemicals.
4. As a source of hydrogen during the cracking process.

Review Questions: Alkanes

 
 2. ALKENES

Alkenes are hydrocarbons which contain at least one double bond between two carbon
atoms in a molecule . The first member of the series is ethene C2H4. because at least two
carbon atoms are necessary for a double bond to be formed.

The First members of the alkene series

Each alkene differs from the next one by a –CH2. group, and conforms to the general
formula CnH2n where n represents the number of carbon atoms in a molecule (n =
2, 3, 4, 5…).

The presence of a double bond in alkenes results in unsaturation. The double bond in
alkenes is easily broken to accommodate more atoms. The C = C double bond determines
the chemical properties of alkenes.

A functional group is an atom or group of atoms which is responsible for the characteristic
reactions of a compound.

Nomenclature
The longest straight chain in alkenes is that which contains the C– C double bond. All
alkenes have names ending with – ene. To name them, a prefix indicating the number of
carbon atoms in the longest straight chain is followed by the suffix – ene.

Naming of alkenes is based on the following rules:

1. To determine the parent name of the alkene identify the longest carbon chain
containing the double bond.

2. 2.    Number the carbon atoms in the longest carbon chain starting from the end
nearer to the double bond. The double bond should be given the lowest possible
number.

In the two cases, the double bond is between carbon 1 and carbon 2. In naming the lower
position is used.
 3. Indicate the positions of the substituent groups by showing the position of the
carbon atom to which they are attached. For example:

The structure should be:

Examples

Isomerism in Alkenes
Alkenes show branching, and positional isomerism.

Branching isomerismoccurs when a substituent group is attached to one of the carbon atoms
in the longest chain containing the double bond.

For example, the branched isomer of but-1-ene is:

Pentene has two branched isomers:

Positional isomerism occurs when the position of the double bond in an alkene

changes. For example:

Laboratory preparation of alkenes.

Alkenes can be prepared by dehydrating their corresponding alkanols using

concentrated sulphuric acid or aluminum oxide.

For example, ethene can be prepared by dehydrating ethanol using concentrated sulphuric
acid or aluminium oxide. The mixture of ethanol and concentrated sulphuric acid or
aluminum oxide must be heated to a temperature of 170°C.

1. Dehydratingethanol with concentrated sulphuric acid.

The ratio of ethanol to concentrated sulphuric acid is 1:2 respectively.

Discussion Questions.
 1. Write an equation for the reaction between ethanol and concentrated
sulphuric acid.

The removal of water molecules from ethanol is a dehydration process. Conc. sulphuric acid
is a dehydrating agent.

2. What is the purpose of the broken porcelain in the reaction flask?

Broken porcelain or sand is used to prevent bumping which may result in cracking of the
flask.

3. Why was sodium hydroxide solution used in the experiment?

The gas produced is passed through sodium hydroxide to remove sulphur(IV) oxide and
carbon(IV) oxide which are formed when concentrated sulphuric acid and ethanol
decompose respectively due to heat.

4. What property of ethene gas enables one to use the above method of
collecting it?

Ethene is slightly soluble in water hence is collected over water.

5. Why is it preferable to use a sand bath instead of heating the round-

bottomed flask directly.

To prevent bumping which may result in cracking of the flask.

6. Explain how aluminium oxide is used to prepare ethene.

The aluminium oxide acts both as a catalyst as well as a dehydrating agent.

Physical Properties
 Ethene is a colourless and oduorless gas.
 It is slightly soluble in water hence is collected over water.
 The solubility of alkenes decreases with increase in molecular mass.Ethene is very
soluble in organic solvents such as methylbenzene, and tetrachloromethane.
  The melting point, and boiling points of alkenes generally increase with increase
in the number of carbon atoms due to an increase in inter-molecular forces,
hence, high boiling and melting points.

Chemical Properties
Alkenes are more reactive than alkanes due to the presence of the double bond. The double
bond is the reactive site of alkenes.

(i) Combustion
All alkanes burn in air with a yellow sooty flame because they are unsaturated. They
have a higher carbon to hydrogen ratio than alkanes.

Since alkenes burn with a sooty flame, they are not preferred for use as fuels.

C2H4(g) + 3O2(g) → 2CO2(g) + 2H2O(l)

(ii) Addition reactions

Ethene undergoes addition reactions because of the double bond. An addition reaction is
one in which one molecule adds to another to form a single product.

(a) Halogenation
This is the addition of halogen atoms across a double bond. Chlorine and bromine are
decolourised immediately when ethene is added. Equations for the reactions are:

(iii)   When bromine is dissolved in water, and reacted with ethene, the following reaction
takes place:

Bromine water is decolourised. This is a test for alkenes.

(b) Hydrohalogenation
Addition of hydrogen halides such as hydrogen bromide, and hydrogen chloride is as shown:

(c) Hydrogenation
Hydrogen gas reacts with ethene at high temperature in the presence of palladium or nickel
catalyst to form ethane.

When hydrogen gas is passed through liquid vegetable and animal oil heated to a
temperature of 180°C, in the presence of a nickel catalyst, solid fat is formed. Therefore this
process of hydrogenation is used in the manufacture of margarine to make the oils solid.

(ii) Self-addition reaction (polymerisation)

Ethene molecules have the ability to react with each other to form a larger molecule which
has a higher molecular mass. Each molecule of ethene is known as a monomer. When
many monomers are joined together, they form a polymer. The following equation shows
how a polymer is formed:

The process in which several monomers combine to form a polymer is referred to

as polymerisation.

When ethene molecules join with each other this way, they form a polymer known as
polyethene. This polymerisation process can be represented by a general equation;

Where n = 2, 3, 4, 5..

(iii) Addition reactions with oxidising agents

(a) Potassium manganate(VII), KMnO4

When ethene is bubbled into acidified potassium manganate(VII) solution, the colour of
the solution turns from purple to colourless.The manganate(VII) is an oxidising agent
and it adds oxygen at the double bond. The manganate(VII) ion is reduced to
manganese(II) ions and water.

This is also another test for alkenes. The equation is:

(b) Acidified potassium chromate(VI) (K4Cr2O7)

When the potassium dichromate(VI) is used in the reaction the orange colour of the
chromate(VI) changes to green. Potassium chromate(VI) acts as an oxidising agent adding
oxygen at the double bond. The chromate(VI) ions are reduced to chromium(III)
ions(Cr3+).

(c) Reaction with concentrated sulphuric acid

Ethene reacts with concentrated sulphuric acid at room temperature to form ethyl hydrogen
sulphate.

When ethyl hydrogen sulphate is added to water, and warmed, the product formed is
ethanol.

Ethyl hydrogen sulphate is hydrolysed to ethanol. This process is referred to as hydrolysis.

Hydrolysis is the reaction of a compound with water such that the hydroxyl group
of the water remains intact.

Generally, the hydrogen atom is added first to ethene molecule to break the double bond,
then the hydroxyl group is added.

Tests for Alkenes

The addition reactions of alkenes with bromine water, acidified potassium manganate (VII)
or acidified potassium(VI) dichromate can be used to test for the presence of a double bond.
Uses of Alkenes
1. In the manufacture of plastics.
2. In the manufacture of ethanol through hydrolysis reactions.
3. In the ripening of fruits (ethene).
4. In the manufacture of detergents.
5. In the laboratory preparation of ethan –1,2 –diol (glycol) which is used as in
coolant (especially as an engine coolant).

Review Questions: Alkenes

3. ALKYNES
Alkynes are hydrocarbons which contain a carbon – carbon triple bond (–C≡C–) in the
molecule.

Each alkyne differs from the next by a –CH2 group and conforms to the general formula,
CnH2n-2, where ‘n’ represents the number of carbon atoms in a molecule, (n = 2,
3, 4…).

The first alkyne member is n = 2 because at least two carbon atoms are necessary for the
formation of a triple bond. The presence of the triple bond results in unsaturation.

Nomenclature
All alkynes have names ending in –yne.

To name them, a prefix indicating the number of carbon atoms in the longest straight chain
is followed by the suffix –yne.
The longest continuous carbon chain must contain the carbon-carbon triple bonds. This
chain is numbered such that the carbon atoms having the triple bond have the lowest
possible value as shown in the examples below.

Isomerism in Alkynes
Alkynes show branching isomerism, and positional isomerism.

(a) Branching Isomerism

This occurs when a substituent group is attached to the longest chain containing the carbon
– carbon triple bond.

For example the branched isomer of pent-l-yne is:

(b) Positional Isomerism

The position of the triple bond in an alkyne molecule can change. This results in the
formation of two or more compounds with the same molecular formula but different
structural formula.

For example:

Ethyne and propyne do not show positional isomerism.

Laboratory Preparation of Ethyne

 Calcium carbide reacts with water at room temperature to form ethyne and calcium
hydroxide.

CaC2(s) + 2H2O(l) → C2H2(g) + Ca(OH)2(aq)

 A layer of sand is placed at the base of the flask because the reaction is highly
exothermic. The sand absorbs the excess heat and therefore prevents the flask
from breaking.
  The flask must be dry before the start of the experiment to avoid formation of
the gas before the set-up is complete.

Physical Properties
Ethyne is a colourless gas and has a pleasant smell when pure. It is slightly soluble in water,
and therefore can be collected over water. The solubility of alkynes is higher in non-polar
solvents. The table below gives some properties of alkynes.

Alkynes with lower molecular mass are gases at room temperature. While those with a
higher molecular mass are solids.

Chemical Properties
Ethyne burns in air, and also undergoes addition reactions.

(a) Combustion
Ethyne like any other hydrocarbon will burn in air to form an oxide of carbon, and water.
This reaction is usually accompanied by production of a lot of heat, therefore, it is preferably
used in oxy-acetylene flames.

In a limited supply of air, ethyne undergoes incomplete combustion to form a mixture of

carbon and carbon(II) oxide. The yellow sooty flame observed is due to
the unburnt carbon.

In excess air, ethyne burns completely to form carbon(IV) oxide and water.

(b) Addition Reactions

Addition reactions in alkynes are faster than in alkenes due to the presence of the triple
bond.

(i) Reaction with hydrogen (hydrogenation)

Ethyne reacts with hydrogen in the presence of a nickel catalyst to form first ethene, then
ethane.

(ii) Reaction with halogens (halogenation)

When ethyne reacts with red-brown bromine vapour, the bromine vapour is

decolourised. The decolourisation process is faster in ethyne than in ethene. The bromine
atoms are added to the carbon-carbon triple bond to form 1, 1, 2, 2,-tetrabromoethane.
This reaction takes place at room temperature and it is a two-step reaction. Thus:

Pure chlorine reacts with ethyne with a violent explosion forming carbon, and hydrogen
chloride.

C2H2 + Cl2(g) → 2C(s) + 2HCl(g)

When diluted with an inert gas, chlorine reacts with ethyne to from 1, 1, 2, 2-
tetrachloroethane in a two step reaction.

(iii) Reaction with hydrogen halides (Hydrohalogenation)

Ethyne does not react with all the hydrogen halides. Hydrogen iodide reacts readily at room
temperature, hydrogen bromide reacts when warmed while hydrogen chloride reacts slowly.

(ii) Hydrogen bromide reacts with ethyne to produce 1,1–dibromoethane (CH3CHBr2)

(iii) The reaction between hydrogen chloride gas is slow.

Test for Alkynes

The test for an alkynes is similar to the tests for alkenes in which the oxidising agents are
decolourised. However, the reaction is faster in alkynes than in alkenes.
Uses of Alkynes
1. They are used in the industrial manufacture of compounds such as adhesives, and
plastics.
2. In the manufacture of synthetic fibres such as rayon.
3. In the production of important chemical reagents and solvents, in which it is used
as a starting material.
4. They are used in the oxy-acetylene flame which is used for welding, and cutting
metals.

Review Questions: Alkynes