Consider the organohalides A and B, where C―I bonds can undergo bond cleavage to form a carbocation and an iodide anion. Predict which organohalide (A or B) would undergo this process at a faster rate. Provide an explanation for your answer.

• A. Organohalide A would undergo the process faster due to the presence of an allylic carbocation intermediate.
• B. Organohalide B would undergo the process faster due to the presence of a more stable tertiary carbocation intermediate.
• C. Organohalide A would undergo the process faster due to the presence of a more sterically hindered carbocation intermediate.
• D. Organohalide B would undergo the process faster due to the less sterically hindered carbocation intermediate.

Answer: (A)