Q6 / 75 · JEE Main 2026 (04 April Shift 2) · Chemistry
Match the LIST-I with LIST-II
List-I (Reaction) List-II (Mechanism) A. Williamson Synthesis I. Electrophilic addition B. Friedel Craft Reaction II. Free radical substitution C. Bromination of vinyl benzene III. Nucleophilic substitution D. Chlorination of toluene in light IV. Electrophilic substitution
Choose the correct answer from the options given below:
| List-I (Reaction) | List-II (Mechanism) |
|---|---|
| A. Williamson Synthesis | I. Electrophilic addition |
| B. Friedel Craft Reaction | II. Free radical substitution |
| C. Bromination of vinyl benzene | III. Nucleophilic substitution |
| D. Chlorination of toluene in light | IV. Electrophilic substitution |
Choose the correct answer from the options given below:
- AA-III, B-I, C-II, D-IV
- BA-III, B-IV, C-II, D-I
- Correct answerCA-III, B-IV, C-I, D-II
- DA-I, B-III, C-IV, D-II
Solution
Williamson synthesis involves the reaction of an alkyl halide with a sodium alkoxide to form an ether, which proceeds via a nucleophilic substitution ($S_N2$) mechanism. Thus, A matches with III.
Friedel-Crafts reaction involves the alkylation or acylation of an aromatic ring in the presence of a Lewis acid catalyst, which proceeds via an electrophilic substitution mechanism. Thus, B matches with IV.
Bromination of vinyl benzene (styrene) involves the addition of bromine across the carbon-carbon double bond, which proceeds via an electrophilic addition mechanism. Thus, C matches with I.
Chlorination of toluene in the presence of sunlight (or UV light) involves the substitution of hydrogen atoms in the methyl group by chlorine, which proceeds via a free radical substitution mechanism. Thus, D matches with II.
The correct matching is A-III, B-IV, C-I, D-II.
Answer: A-III, B-IV, C-I, D-II
Friedel-Crafts reaction involves the alkylation or acylation of an aromatic ring in the presence of a Lewis acid catalyst, which proceeds via an electrophilic substitution mechanism. Thus, B matches with IV.
Bromination of vinyl benzene (styrene) involves the addition of bromine across the carbon-carbon double bond, which proceeds via an electrophilic addition mechanism. Thus, C matches with I.
Chlorination of toluene in the presence of sunlight (or UV light) involves the substitution of hydrogen atoms in the methyl group by chlorine, which proceeds via a free radical substitution mechanism. Thus, D matches with II.
The correct matching is A-III, B-IV, C-I, D-II.
Answer: A-III, B-IV, C-I, D-II
Hence, the correct answer is option: 'C'.