Which of the following undergoes hydrolysis m | vedclass

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(D) The rate of nucleophilic aromatic substitution (hydrolysis) increases with the number of electron-withdrawing groups (like $-NO_2$) present on the

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(D) The rate of nucleophilic aromatic substitution (hydrolysis) increases with the number of electron-withdrawing groups (like $-NO_2$) present on the benzene ring. These groups decrease the electron density on the ring through $-I$ and $-M$ effects,thereby facilitating the attack of the nucleophile. Since $1-Chloro-2,4,6-trinitrobenzene$ has the maximum number of $-NO_2$ groups (three),it undergoes hydrolysis most easily.

Which of the following undergoes hydrolysis most easily?

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