Para nitro chloro benzene undergoes nucleophilic substitution faster than chlorobenzene by
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In Chlorobenzene, the Negative Charge is delocalized inside the ring whereas, in the p-Nitrochlorobenzene, the presence of Strong Electron withdrawing Group like Nitro more delocalizes the charge because it comes on the Electronegative O atom. We know that more is that the delocalization, more is that the resonance, the Stable is that the intermediate Product formed and therefore more is that the rate of reaction.
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