Answer:
See figure 1
Explanation:
In this question, we have to start with the <u>protonation of the double bond</u>. In carvone we have two double bonds, so, we have to decide first which one would be protonated.
The problem states that the <u>terminal alkene</u> is the one that would is protonated. Therefore, we have to do the <u>protonation</u> in the double bond at the bottom to produce the <u>carbocation number 1</u>. Then, a hydride shift takes place to produce the <u>carbocation number 2</u>. A continuation, an <u>elimination reaction</u> takes place to produce the <u>conjugated diene</u>. Then the diene is protonated at the <u>carbonyl group</u> and with an elimination reaction of an hydrogen in the <u>alpha carbon</u> we can obtain <u>carvacol. </u>
