Answer: B
The alcohol is 2-methylbutan-2-ol, which reacts by E1 through a tertiary cation. Loss of a hydrogen from the CH2 group gives the trisubstituted 2-methylbut-2-ene (Saytzeff), more stable than the disubstituted 2-methylbut-1-ene. 3-Methylbut-1-ene would need a rearrangement.