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

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.

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.

We expect to get one major product because the bromine radical will preferentially abstract the most stable hydrogen from the benzylic carbon.

We expect to get one major product because the bromine radical will preferentially abstract the most stable hydrogen from the benzylic carbon.