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Why products arediffer,when 1-naphthol,2-naphthol are treated with Na/iso-C5H5O11(reduction)?

Mary George , 6 Years ago
Grade 12th pass
anser 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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