Draw the structure of the major monohalo product for each of the following reactions: 
The reaction is a heat-induced bromination, yielding a benzylic bromination product. Specifically, a bromine atom substitutes the hydrogen on the benzylic carbon (adjacent to the benzene ring), forming 1-bromo-2-phenylethane as the primary product. The product's structure is:
\[ \text{C}_6\text{H}_5\text{CH}_2\text{CH}_2\text{Br} \]
Given below are two statements:
Statement (I): Alcohols are formed when alkyl chlorides are treated with aqueous potassium hydroxide by elimination reaction.
Statement (II): In alcoholic potassium hydroxide, alkyl chlorides form alkenes by abstracting the hydrogen from the $ \beta $-carbon.
In the light of the above statements, choose the most appropriate answer from the options given below: