Which among the following compounds reacts wi | vedclass

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(C) The reaction of aryl halides with $NaOH$ proceeds via Nucleophilic Aromatic Substitution $(S_NAr)$.This reaction is facilitated by the presence of

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$2,4,6$-Trinitrochlorobenzene

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(C) The reaction of aryl halides with $NaOH$ proceeds via Nucleophilic Aromatic Substitution $(S_NAr)$.This reaction is facilitated by the presence of electron-withdrawing groups ($-M$ effect) at the ortho and para positions,which stabilize the intermediate Meisenheimer complex.As the number of electron-withdrawing $-NO_2$ groups increases,the rate of the $S_NAr$ reaction increases.$2,4,6$-Trinitrochlorobenzene has three electron-withdrawing $-NO_2$ groups,making it the most reactive towards nucleophilic substitution.

Which among the following compounds reacts with $NaOH$ at the fastest rate?

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