Acid catalysed conversation of 1,2-diol or vicinal, into carbonyl compound known as pinocaol-pinacolone rearrangement.

Generally more electron donating group migrate during mechanism, migration of H is faster because of its smaller size.
What would be the major product of reaction?

Acid catalysed conversation of 1,2-diol or vicinal, into carbonyl compound known as pinocaol-pinacolone rearrangement. Generally more electron donating group migrate during mechanism, migration of H is faster because of its smaller size. In this sequence of reaction final product is"

Acid catalysed conversation of 1,2-diol or vicinal, into carbonyl compound known as pinocaol-pinacolone rearrangement. Generally more electron donating group migrate during mechanism, migration of H is faster because of its smaller size. Which of the following is not correct about this rearrangement?

Acid catalysed conversation of 1,2-diol or vicinal, into carbonyl compound known as pinocaol-pinacolone rearrangement. Generally more electron donating group migrate during mechanism, migration of H is faster because of its smaller size. Which of the following is not correct about this rearrangement?

The base catalysed reaction of 1,2-diketone to a salt of 2-hydroxy carbonxylic acid is known as benzile acid rearrangement . The reaction is not application to 1,2-diketones containing alpha- methylene group because of competing aldol condensation . Find out product of following reaction :