Why products arediffer,when 1-naphthol,2-naphthol are treated with Na/iso-C5H5O11(reduction)?
Mary George , 6 Years ago
Grade 12th pass
1 Answers
Pooja
Last Activity: 5 Years ago
Dear Student, This is because in the 1-naphthol, the adjacent ring is at the ortho position and it is more activated towards hydrogenation as it is elecron rich. In 2-naphthol the ring is meta to the OH group and therefore it is not activated and hence the ring containing the OH group is reduced.
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