Draw the structure of the major monohalo product for each of the following reactions:
The reaction involves a bromination in the presence of heat, which typically leads to the formation of a benzylic bromination product. In this case, the hydrogen at the benzylic position (the carbon adjacent to the benzene ring) will be replaced by a bromine atom, forming 1-bromo-2-phenylethane as the major product. The structure of the product is:
\[ \text{C}_6\text{H}_5\text{CH}_2\text{CH}_2\text{Br} \]
The major product (A) is:
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: