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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:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8204/13th_html_m36b9760c.gif

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:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8204/13th_html_721aa7c7.gif

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

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8204/13th_html_m122b86c9.gif

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:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8204/13th_html_1466dda1.gif

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:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8204/13th_html_2b99005c.gif

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. https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_6eccc78a.gif

b. https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_615145f0.gif

c. https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_67a45048.jpg

d. https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_m1f2abc8.jpg

e. https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_7912f1ef.jpg

f.

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_c2545a6.gif

g.

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_m7e0d0778.gif

Answer:

(a)

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_65974dfc.gif

IUPAC name: 2-Methylbut-2-ene

(b) https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_m28e8f111.gif

IUPAC name: Pen-1-ene-3-yne

(c) https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_67a45048.jpg  can be written as:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_m47c17e0.gif

IUPAC name: 1, 3-Butadiene or Buta-1,3-diene

(d)

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_m1f2abc8.jpg

IUPAC name: 4-Phenyl but-1-ene

(e) https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_m271ee.jpg

IUPAC name: 2-Methyl phenol

(f)

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_700e61ff.gif

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

(g)

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/8197/13th_html_m6d5a4157.gif

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:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4029/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_190042e1.gif

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4029/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_m42faeee8.gif

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4029/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_m1c7bd249.gif

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:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4029/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_m6a919120.gif

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4029/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_374a460a.gif

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4029/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_4882706b.gif

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:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4030/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_1d5e472c.jpg

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

(ii) 3, 4-Dimethylhept-3-ene undergoes ozonolysis as:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4030/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_m4322b8c2.jpg

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:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4030/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_33a44c55.jpg

The IUPAC name of Product (I)is pentan-3-one and Product (II)is methanal.

(iv) 1-Phenylbut-1-ene undergoes ozonolysis as:

https://img-nm.mnimgs.com/img/study_content/curr/1/11/13/206/4030/NCERT_SOLUTION_1-10-08_Vidushi_11_Chemistry_13_25_SJT_html_m69d02ca3.jpg

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