Bacause of the resonance stabilization of Arylhalides they are unreactive toward normal nuclephilic substitution reactions . However arylhalides having strong electron withdrawing groups at ortho and para positions give aromatic nucleophilic substitution reactions `(S_(N)Ar` mechanism ) , which involves a resonance stablilized carbanion called Meisenheimer complex Which arylhalide is most reactive toward `S_(N)Ar` mechanism ?A. B. C. D.

Bacause of the resonance stabilization of Arylhalides they are unreact

1.	Bacause of the resonance stabilization of Arylhalides they are unreactive toward normal nuclephilic substitution reactions . However arylhalides having strong electron withdrawing groups at ortho and para positions give aromatic nucleophilic substitution reactions `(S_(N)Ar` mechanism ) , which involves a resonance stablilized carbanion called Meisenheimer complex Which arylhalide is most reactive toward `S_(N)Ar` mechanism ?A. B. C. D.
Answer» Correct Answer - A

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