What is the product obtained when benzonitril | vedclass

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(B) The reaction of benzonitrile $(C_6H_5CN)$ with phenylmagnesium bromide $(C_6H_5MgBr)$ in dry ether proceeds via a nucleophilic addition to the nit

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Benzophenone

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(B) The reaction of benzonitrile $(C_6H_5CN)$ with phenylmagnesium bromide $(C_6H_5MgBr)$ in dry ether proceeds via a nucleophilic addition to the nitrile group.First,the phenyl group from the Grignard reagent attacks the electrophilic carbon of the nitrile,forming an imine complex intermediate: $C_6H_5CN + C_6H_5MgBr \rightarrow C_6H_5-C(C_6H_5)=N-MgBr$.Subsequently,acid-catalyzed hydrolysis $(H_3O^+)$ of the imine complex converts the $C=N-MgBr$ group into a carbonyl group $(C=O)$,yielding benzophenone $(C_6H_5-CO-C_6H_5)$ as the final product along with ammonia and magnesium salts.

What is the product obtained when benzonitrile is treated with $C_6H_5MgBr$ in dry ether and then hydrolyzed?

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