Answer:
See explanation
Explanation:
The mechanism involves SN1 nucleophilic substitution reaction. The -OH group of the alcohol is first protonated. Since water is a good leaving group, -OH2 leaves the substrate creating a primary carbo cation.
A 1,2 methyl shift now occurs to create a tertiary carbo cation which is more stable leading to the major product shown in the image attached to this answer.
