The Baeyer-Villiger oxidations of the substituted diphenyl ketones proceeds as indicated because:
A. The electron-withdrawing nitro group retards the migration of the phenyl ring to which it is attached.
B. The electron-releasing methoxy group accelerates the migration of the phenyl ring to which it is attached.
C. Both A and B
D. Neither A nor B. The regiospecificity is due to steric effects in the migrating group.
We need at least 10 more requests to produce the solution.
0 / 10 have requested this problem solution
The more requests, the faster the answer.