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(B) The reaction involves the acid-catalyzed dehydration of an alcohol. $1$. Protonation of the $-OH$ group followed by the loss of water forms a seco

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(B) The reaction involves the acid-catalyzed dehydration of an alcohol. $1$. Protonation of the $-OH$ group followed by the loss of water forms a secondary carbocation. $2$. This secondary carbocation undergoes a $1,2-H$ shift to form a more stable tertiary carbocation. $3$. The tertiary carbocation then loses a proton from the adjacent carbon to form the most stable alkene according to Saytzeff's rule. $4$. The final product is $2,3-dimethylpent-2-ene$.

What is the major product of the following reaction?

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