Final answer:
The reaction of 4-methoxyphenol with 4-bromobenzyl bromide likely involves nucleophilic aromatic substitution to form an ether product; however, without detailed reaction conditions, the specific outcome is uncertain.
Step-by-step explanation:
The reaction of 4-methoxyphenol with 4-bromobenzyl bromide typically involves a nucleophilic aromatic substitution where the 4-methoxyphenol acts as the nucleophile and the 4-bromobenzyl bromide acts as the electrophile. There are many possible products due to the different positions on the phenol ring where substitution can occur. However, without specific conditions such as solvents, catalysts, temperature, and reaction time, it's not possible to accurately predict the major product of this reaction. If desired, this reaction could potentially yield a corresponding ether where the 4-methoxyphenol oxygen atom attaches to the benzylic carbon of the 4-bromobenzyl bromide, eliminating a molecule of hydrogen bromide (HBr) in the process.