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B
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C
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D
No reaction
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Solution
The correct option is A The given reaction is an electroophilic aromatic substitution reaction. In the reactant molecule we have both OH and CH3 substituents.
Since, −OH group is a stronger ortho para directing than CH3 due to its +R effect, the electrophile will get substituted at ortho/para position of OH group.
Since, the para position is already blocked by methyl, the NO2 gets added to the ortho position of OH.
Hence, option (a) is correct.