Show how the following compound can be synthesized using free-radical halogenation. Explain why only one major product is expected. (Ignore stereochemistry.)

• A. We expect to get one major product because the position of the hydrogen makes it easy to abstract without the aid of the bromine radical.
• B. We expect to get one major product because the position of the hydrogen makes it easy to abstract without the aid of the bromine radical.
• C. We expect to get one major product because the bromine radical will preferentially abstract the most stable hydrogen from the benzylic carbon.
• D. We expect to get one major product because the bromine radical will preferentially abstract the most stable hydrogen from the benzylic carbon.