What will be the major product in the given r | vedclass

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(A) The given reaction is the Gabriel phthalimide synthesis. In the first step,phthalimide reacts with $KOH$ to form potassium phthalimide. In the sec

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(A) The given reaction is the Gabriel phthalimide synthesis. In the first step,phthalimide reacts with $KOH$ to form potassium phthalimide. In the second step,potassium phthalimide acts as a nucleophile and undergoes an $S_N2$ reaction with the alkyl halide. The alkyl halide provided is $4-bromobenzyl  chloride$ $(Br-C_6H_4-CH_2Cl)$. Since the $CH_2Cl$ group is more reactive towards $S_N2$ substitution than the aryl bromide $(C-Br)$,the nucleophilic attack occurs at the $CH_2Cl$ site. Therefore,the nitrogen of the phthalimide replaces the chlorine atom,resulting in $N-(4-bromobenzyl)phthalimide$ as the major product.

What will be the major product in the given reaction?

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