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when we add ortho-bromoanisole in NaNH2 + NH3 we form products using the benzyne mechanism.mechanism from my textbook

here, we form the products considering only -I effect of -OCH3, if we consider its +M effect we would form, o-Anisidine, why is +M effect ignored here? is it because of sp2 hybridization of carbanion, if so, how?

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    $\begingroup$ Is the anion electron pair in conjugation with the lone pairs on the oxygen atom? $\endgroup$ Nov 30 '21 at 16:56

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