Which of the following aryl halides will react with sodamide/ liquid ammonia leading to substitution via benzyne mechanism
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option "d " hai
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Answer:
Option (A) is the correct answer.
Explanation:
We discovered that electron-poor aromatic rings with a leaving group can be substituted by electron-rich nucleophiles. We saw how the mechanism works by first adding a nucleophile to the aromatic ring (via an electron-rich intermediate), then losing a leaving group. This distinguishes it from electrophilic aromatic substitution, which produces a mixture of ortho-, para–, and meta- products.
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