INTRODUCTION - Chapter 13 - Hydrocarbons - Ncert Solutions class 11 - Chemistry
Updated On 26-08-2025 By Lithanya
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Question 13.1:
How do you account for the formation of ethane during chlorination of methane?
Answer:
Chlorination of methane proceeds via a free radical chain mechanism. The whole reaction takes place in the given three steps.
Step 1: Initiation:
The reaction begins with the homolytic cleavage of Cl – Cl bond as:

Step 2: Propagation:
In the second step, chlorine free radicals attack methane molecules and break down the C–H bond to generate methyl radicals as:

These methyl radicals react with other chlorine free radicals to form methyl chloride along with the liberation of a chlorine free radical.

Hence, methyl free radicals and chlorine free radicals set up a chain reaction. While HCl and CH3Cl are the major products formed, other higher halogenated compounds are also formed as:

Step 3: Termination:
Formation of ethane is a result of the termination of chain reactions taking place as a result of the consumption of reactants as:

Hence, by this process, ethane is obtained as a by-product of chlorination of methane.
Question 13.2:
Write IUPAC names of the following compounds:
a. 
b. 
c. 
d.
e.
f.

g.

Answer:
(a)

IUPAC name: 2-Methylbut-2-ene
(b)
IUPAC name: Pen-1-ene-3-yne
(c)
can be written as:

IUPAC name: 1, 3-Butadiene or Buta-1,3-diene
(d)

IUPAC name: 4-Phenyl but-1-ene
(e) 
IUPAC name: 2-Methyl phenol
(f)

IUPAC name: 5-(2-Methylpropyl)-decane
(g)

IUPAC name: 4-Ethyldeca-1, 5, 8-triene
Question 13.3:
For the following compounds, write structural formulas and IUPAC names for all possible isomers having the number of double or triple bond as indicated:
(a) C4H8 (one double bond)
(b) C5H8 (one triple bond)
Answer:
(a) The following structural isomers are possible for C4H8 with one double bond:



The IUPAC name of
Compound (I) is But-1-ene,
Compound (II) is But-2-ene, and
Compound (III) is 2-Methylprop-1-ene.
(b) The following structural isomers are possible for C5C8 with one triple bond:



The IUPAC name of
Compound (I) is Pent-1-yne,
Compound (II) is Pent-2-yne, and
Compound (III) is 3-Methylbut-1-yne.
Question 13.4:
Write IUPAC names of the products obtained by the ozonolysis of the following compounds:
(i) Pent-2-ene (ii) 3,4-Dimethyl-hept-3-ene
(iii) 2-Ethylbut-1-ene (iv) 1-Phenylbut-1-ene
Answer:
(i) Pent-2-ene undergoes ozonolysis as:

The IUPAC name of Product (I) is ethanal and Product (II)is propanal.
(ii) 3, 4-Dimethylhept-3-ene undergoes ozonolysis as:

The IUPAC name of Product (I)is butan-2-one and Product (II)is Pentan-2-one.
(iii) 2-Ethylbut-1-ene undergoes ozonolysis as:

The IUPAC name of Product (I)is pentan-3-one and Product (II)is methanal.
(iv) 1-Phenylbut-1-ene undergoes ozonolysis as:

The IUPAC name of Product (I)is benzaldehyde and Product (II)is propanal.
