3.3. Organic Chemistry I-2
3.3. Organic Chemistry I-2
3.3. Organic Chemistry I-2
ORGANIC CHEMISTRY I
(HYDROCARBONS)
By the end of this chapter, the learner should be able to:
(a) Define organic chemistry.
(b) Define hydrocarbons and classify them according to their structure and bonding.
(c) Write molecular and structural formulae of alkanes, alkenes and alkynes.
(d) Name and draw the structures of alkanes, alkenes and alkynes.
(e) Define an isomer, name and draw the structures of the isomers of hydrocarbons
with up to five carbon atoms in their molecules.
(f) Describe the general methods of preparing different hydrocarbons.
(g) Explain the gradual change in properties among the members of a homologous
series.
(h) State some uses of hydrocarbons.
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
hydrogen atoms only.
They are classified into three groups depending on the type of bond that exists
between 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
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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.
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.
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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.
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Isomerism in Alkanes
Isomers are 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, Butyl,
CH3CH2CH2CH3 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,
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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
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.
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.
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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:
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.
Sand
Alkaline
Gas G
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.
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.
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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.
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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.
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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 alkenes 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)
(a) Halogenation
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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:
(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.
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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.
Where n = 2, 3, 4, 5..
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+).
When ethyl hydrogen sulphate is added to water, and warmed, the product formed is
ethanol.
Uses of Alkenes
1. In the manufacture of plastics.
2. In the manufacture of ethanol through hydrolysis reactions.
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Ca(0H)2
Cl H
Step 3
L + H20 1 mole HCL K C C
Gas J H H
Step 1 Step 2
R
1 mole H2
Step 4
3. ALKYNES
Alkynes are hydrocarbons which contain a carbon – carbon triple bond (–
C≡C–) in the molecule.
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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.
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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.
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:
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.
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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.
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.
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.
3. Draw the open structure of the compound with the following molecular
structure: C6H10
4. The reaction between bromine vapour and ethyne is faster than with
ethene. Explain.
5. The relative formula mass of a hydrocarbon is 58. Draw and name two
possible structures of the hydrocarbon (C=12.0; H=1.0
6. Alkanes, alkenes and alkynes can be obtained from crude oil. Draw the
structure of the second member of the alkyne homologous series.
7. Draw and name the structure of the compound formed when one Mole
of ethyne reacts with one mole of hydrogen bromide.
8. Draw the structures of the alkynes whose molecular formula is C 4H6
9. Study the flowchart below and answer the questions that follow:
water
C2H2 X
HCl
Process Z
Polyvinylchloride
(b) Give the uses of the four hydrocarbons named in (a) above.
(c) Explain with the help of a suitable diagram, the principles used in
separating hydrocarbons in crude oil.
2. What do you understand by the following terms:
(a) Catalytic cracking.
(b) Thermal cracking.
3. Study the following reaction scheme and answer the questions that
follow:
(a) Name:
(i) Colourless gas A.
(ii) Product B.
(iii) Gas D.
(iv) Liquid E.
(b) Write balanced equations for each of the reactions forming the
products in (a).
(c) Name the type of reactions taking place in Step I and II.
(d) State the importance of the reaction taking place in Step II.
4. Explain why an organic compound with formula C 3H6 burns with a more
sooty flame than C3H8
5. Butane and bromine react as shown below:
CH3,CH2.CH2CH3 + Br2 → CH3CH2.CH2Br + HBr
(a) Name the type of reaction taking place in the equation above.
(b) State the condition under which the above reaction takes place.
Explain.
6. A hydrocarbon Q, was found to decolourise potassium manganate(VII)
solution. When two moles of Q are burnt completely, six moles of
carbon(IV) oxide and six moles of water were formed.
(a) Write the structural formula of Q.
(b) Name the homologous series to which Q belongs.
(c) Name one industrial source of Q.
7. The diagram below shows the combustion of ethane gas.
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