Concept:
Alcoholic KOH promotes elimination reactions (E2 mechanism) in alkyl halides, leading to the formation of alkenes. According to Saytzeff's rule, the more substituted alkene is the major product.
Step 1: Identify the reaction type.
2-bromopentane reacts with alcoholic KOH via β-elimination, removing a hydrogen atom from the β-carbon and bromine from the α-carbon.
Step 2: Apply Saytzeff's rule.
The elimination favors formation of the more substituted alkene. Therefore, pent-2-ene is formed as the major product rather than pent-1-ene.
Thus,
\[
\boxed{\text{Pent-2-ene}}
\]