Which of the following compounds undergoes nu | vedclass

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(A) Nucleophilic aromatic substitution reactions are facilitated by the presence of electron-withdrawing groups on the benzene ring. These groups stab

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p-Nitrochlorobenzene

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(A) Nucleophilic aromatic substitution reactions are facilitated by the presence of electron-withdrawing groups on the benzene ring. These groups stabilize the intermediate carbanion (Meisenheimer complex) formed during the reaction. The $-NO_2$ group is a strong electron-withdrawing group due to its $-I$ and $-M$ effects. In contrast,$-CH_3$ and $-OCH_3$ groups are electron-donating groups,which destabilize the intermediate carbanion and make the reaction more difficult. Therefore,$p$-nitrochlorobenzene undergoes nucleophilic substitution most easily.

Which of the following compounds undergoes nucleophilic substitution reaction most easily?

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