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Question: From the above reactions, the number of reactions that produces benzaldehyde is A. ![](https://www...

From the above reactions, the number of reactions that produces benzaldehyde is
A.
B.
C.
D.

Explanation

Solution

Benzaldehyde is an organic compound consisting of a benzene ring with a formal substituent. The molecular formula C6H5CHO{{C}_{6}}{{H}_{5}}CHO. It is a colorless liquid having an almond-like odor. It can be extracted from a number of other natural sources. Synthetic benzaldehyde is the flavoring agent which is used to flavor cakes and other baked goods.

Complete step by step answer:
All the reactions given above gives benzaldehyde as their product let’s discuss all the reaction one by one
A. This is the example of Gatterman-Koch formylation reaction. In this reaction benzene is treated with COCO and HClHCl under high pressure in the presence of anhydrous AlCl3,CuClAlC{{l}_{3}},CuCl and formed benzaldehyde.

B. This reaction is simply hydrolysis and hydrolysis of benzoyl chloride with water will form benzaldehyde as a product.

C. Reaction shown in option C is a rosenmund reduction. This reaction explains how acyl chlorides are selectively reduced into aldehydes. The Rosenmund reaction is a hydrogenation process where molecular hydrogen reacts with the acyl chloride where palladium or barium sulfate acts as a catalyst in this reaction which enhances the rate of reaction.

D. This reaction is generally a reduction reaction in which partial reduction of methyl benzoate with DIBAL-H in the presence of toluene gives benzaldehyde. Where DIBAL-H is diisobutylaluminium hydride which is generally used as a reducing agent.

From the above discussion we consider that all the reaction gives benzaldehyde as a product.

So the answer should be D.

Note: Benzaldehyde can be oxidized to benzoic acid. The boiling point of benzoic acid is much higher than that of benzaldehyde; it can be purified by a simple process called distillation. Benzyl alcohol can be formed from benzaldehyde by means of hydrogenation.