The reaction of 1,2-dimethylcyclohexene with NBS under UV light produces a mixture of two products.
However, the reaction of cyclopentene with NBS only produces one product despite the generation of a resonance-stabilized radical. Explain why this reaction does not yield a second product.

• A. Multiple products are formed but there is only one major product.
• B. Since one mole of NBS is used, there can only be a single allylic brominated product.
• C. Cycloalkenes with odd number of carbon atoms only produce single products in allylic bromination reactions.
• D. The two allylic radicals formed from cyclopentene are equivalent.