Halogenation of which one of the following wi | vedclass

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Question

(C) In electrophilic aromatic substitution,the incoming electrophile attacks the position that is ortho or para to the most strongly activating group

Vedclass · Accepted Answer

$2-$methylphenol

Vedclass · Answer

(C) In electrophilic aromatic substitution,the incoming electrophile attacks the position that is ortho or para to the most strongly activating group (the group with the strongest electron-releasing effect).For $2$-methylphenol ($o$-cresol),the $-OH$ group is a much stronger activating group than the $-CH_3$ group.The $-OH$ group directs the electrophile to its ortho and para positions.The para position with respect to the $-OH$ group is the meta position with respect to the $-CH_3$ group.Therefore,halogenation of $2$-methylphenol yields the $m$-substituted product with respect to the methyl group as the major product.

Halogenation of which one of the following will yield $m$-substituted product with respect to the methyl group as a major product?

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