Which of the following compounds undergoes nu | vedclass

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(B) Nucleophilic aromatic substitution reactions occur more readily when electron-withdrawing groups (EWGs) are present on the benzene ring. These gro

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$1-$Chloro$-4-$nitrobenzene

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(B) Nucleophilic aromatic substitution reactions occur more readily when electron-withdrawing groups (EWGs) are present on the benzene ring. These groups stabilize the negatively charged intermediate (Meisenheimer complex) formed during the reaction. The $-NO_2$ group is a strong electron-withdrawing group due to its $-I$ and $-M$ effects,which significantly stabilizes the carbanion intermediate. Therefore,$1$-chloro-$4$-nitrobenzene undergoes nucleophilic substitution most easily.

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

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