ALKANES
The alkanes are a homologous series of saturated aliphatic hydrocarbons with a general molecular formula of CnH2n+2. The are the only saturated hydrocarbons because they contain only single bonds. The are found mainly in petroleum. The carbon atoms in the alkanes exhibit sp3 hybridization. There is a gradual change in the physical properties of the members from the gaseous state (for the lighter members) to the liquid state and then the solid state for the heavier compounds.
The first ten members of the series are.
1. methane CH4
2. Ethane C2H6
3. Propane C3H8
4. Butane C4H10
5. Pentane C5H12
6. Hexane C6H14
7. Heptane C7H16
8. Octane C8H18
9. Nonane C9H20
10. Decane C10H22
Chemical properties
The alkanes undergo only two reactions, combustion and substitution reactions
1. Combustion Reaction: - this is a general property for all hydrocarbons. The alkanes burn in air or oxygen to yield Carbon (iv) oxide and water.
CH4(g) + O2(g) → CO2(g) + H2O(g)
2. Substitution Reaction: - Substitution reaction is the only other reactions that the alkanes can undergo because they are saturated.
A Substitution reaction is a reaction where one element (atom) replaces one or more of the hydrogen atoms in an alkane molecule.
METHANE: - This is the first and the simplest member of the alkane family. It has a molecular formula of CH4 and a structural formula of
H
׀
H − C − H
׀
H
It is found naturally in swamps or swampy areas when vegetations and dead organic matter decompose. It is also one of the major components in natural gas
Laboratory Preparation
Methane is prepared in the laboratory by the action of sodium ethanoate on soda- lime. (soda-lime is sodium hydroxide that has been slaked with lime CaO).
Soda- lime is preferred to caustic soda because
1. It is not Deliquescent and
2. It does not attack glass.
Laboratory Preparation of methane
CH3COONa(S) + NaOH(s) → Na2CO3(s) + CH4(g)
Physical properties
i. It is a colourless gas.
ii. It is less dense than air.
iii. It is insoluble in water.
Chemical properties
I. Combustion: - methane burns with a pale blue flame in air or oxygen
CH4(g) + O2(g) → CO2(g) + H2O(l)
2. Substitution reaction: - Methane combines with Chlorine to produce various products.
The reaction is faster in the presence of light (photochemical reaction) and it occurs in stages.
I. CH4(g) + Cl2(g) → CH3Cl + HCl
Mono chloromethane
II. CH3Cl + Cl2(g) → CH2Cl2 + HCl
dichloromethane
III. CH2Cl2 + Cl2(g) → CHCl3 + HCl
trichloromethane
IV. CHCl3 + Cl2(g) → CCl4 + HCl
tetrachloromethane
Uses of Methane
I. It is used mainly as fuel sometimes mixed with other fuels
2. It is used to make hydrogen
3. It is used to make carbon black
4. When refined it is can be used as a rocket fuel
OBJECTIVE QUESTIONS
1. What is the IUPAC name of the compound with this structure
H H H H| | | |
H— C — C — C — C — H
| | | |
H | H H
|
H —C—H
|
H
a. 3-methylbutane
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