Answer:
Option-B (2-methylpropene)
Step-by-step explanation:
The reaction scheme is attached below,
In first step the alkene acts a nucleophile and adds H⁺ across double bond yielding a stable tertiary carbocation.
In the second step the oxygen atom of methanol acts as nucleophile and attacks the positive charge carrying carbon atom resulting in the formation of t-butyl methyl ether.