Which of the following reagent(s) is required for the conversion of Benzene to methyl benzoate?
(A) Br₂ / FeBr₃
(B) Mg, dry Ether
(C) CO₂, H₃O⁺
(D) Methanol, Conc. H₂SO₄
Choose the correct answer from the options given below:
Correct Answer :
(A), (B), (C) and (D)
Solution :
The correct option is (A), (B), (C) and (D).
To convert benzene into methyl benzoate, a multi-step synthetic pathway is required. Each of the given reagents plays a key role in a specific step of the overall transformation as described below:
Step 1: Bromination of Benzene
Benzene is reacted with bromine () in the presence of iron(III) bromide (), which acts as a Lewis acid catalyst. This electrophilic aromatic substitution reaction yields bromobenzene.
This step requires reagent (A) Br2 / FeBr3.
Step 2: Formation of the Grignard Reagent
Bromobenzene is treated with magnesium () metal in the presence of dry ether. This insertion reaction forms phenylmagnesium bromide, which is a nucleophilic Grignard reagent.
This step requires reagent (B) Mg, dry Ether.
Step 3: Carboxylation to form Benzoic Acid
The Grignard reagent is reacted with carbon dioxide () to form a carboxylate salt intermediate. Subsequent acidic workup with hydronium ions () protonates the intermediate to yield benzoic acid.
This step requires reagents (C) CO2, H3O+.
Step 4: Fischer Esterification to form Methyl Benzoate
Finally, benzoic acid is reacted with methanol () in the presence of concentrated sulfuric acid () acting as a catalyst and dehydrating agent. This esterification reaction yields the target compound, methyl benzoate.
This step requires reagents (D) Methanol, Conc. H2SO4.
Thus, all four sets of reagents (A, B, C, and D) are required to complete the conversion sequence from Benzene to methyl benzoate.
Access expert-curated educational resources and study materials—completely free.
Create, conduct, and manage professional online assessments with Mindyard. Perfect for teachers and institutes.
Copyright © 2026 Mindyard. All Rights Reserved.