B-H-Y - B-H-Y

Compound - A (C3H6O) undergoes following reactions to form B and C . Identify A, B and C . C Zn - Hg/HCl AC3H6O I2/NaOH B

SOLVED: Consider the reaction between hydrobromic acid (HBr) and the alkene shown below: You read a claim that Product B is the major product of this reaction.H-BrDraw mechanism for the reaction above that leads to Product A

Reaction of HBr with 3-methylcyclohexene yields a mixture of four products: cis- and trans-1-bromo-3-methylcyclohexane and cis- and trans-1-bromo2-methylcyclohexane. The analogous reaction of HBr with 3-bromocyclohexene yields trans-1,2-dibromocyclohexane as the sole product. Draw structures of the possible intermediates, and then explain why only a single product is formed in the reaction of HBr with 3-bromocyclohexene. | Numerade