Which of the following compounds has difficul | vedclass

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(C) The reactivity of haloarenes towards nucleophilic substitution increases with the presence of electron-withdrawing groups (like $-NO_2$) at the $o

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$m-$Nitrochlorobenzene

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(C) The reactivity of haloarenes towards nucleophilic substitution increases with the presence of electron-withdrawing groups (like $-NO_2$) at the $ortho$ and $para$ positions due to the stabilization of the carbanion intermediate.Electron-withdrawing groups at the $meta$ position have a negligible effect on the reactivity compared to $ortho$ and $para$ positions.Therefore,among the given options,$m-$nitrochlorobenzene is the least reactive,making it the most difficult to break the $C-X$ bond during a nucleophilic substitution reaction.

Which of the following compounds has difficulty in breaking the $C-X$ bond during a nucleophilic substitution reaction?

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