The diene reacts with HBr to give two isomers A and B (C6H11Br).
a. Give the structures of A and B.
b. Give the structure of the carbocation intermediate involved in this reaction. Be sure to show any relevant resonance structures.
c. When compounds A and B are each treated under solvolysis conditions with acetone/water, each compound forms a mixture of the same two alcohols C and D. Give the structures of these two alcohols and explain why both are formed from each alkyl halide.
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