Final answer:
The question involves identifying the products of an allylic bromination reaction using NBS and UV light on 3,3,6-trimethylcyclohexene, which typically leads to a variety of brominated allylic compounds.
Step-by-step explanation:
The question asks about the reaction products when 3,3,6-trimethylcyclohexene is treated with N-bromosuccinimide (NBS) and irradiated with UV light. This reaction typically involves the allylic bromination of the alkene, where NBS selectively brominates the allylic position (the carbon atom next to the double bond) without adding across the double bond itself. As such, the primary product would be the bromine-substituted allylic compound. In the case of 3,3,6-trimethylcyclohexene, multiple allylic positions are present, which could give rise to a mixture of regioisomeric brominated products. The exact products would depend on the positions that the bromine atoms end up adding to, which is determined by the stability of the resulting allylic radicals formed during the reaction process and the reaction's regioselectivity.