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When sec-butylcyclohexane reacts with bromine in the presence of sunlight, the major product is :
In the free radical bromination of sec-butylcyclohexane, bromine selectively attacks the most stable radical intermediate, which is the tertiary ($$3^\circ$$) carbon at the ring junction (Carbon I). This specific position is prioritized over the side-chain tertiary carbon because it is stabilized by a higher number of $$\alpha$$-hydrogen atoms through hyperconjugation.
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