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 What would be the product of the given reaction ? 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 What would be the product of the given reaction ? A. B. C. D.
Answer» Correct Answer - B

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