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SOLVED: N-bromosuccinimide (NBS) reacts with alkenes to form allylic halides. The reaction follows a three-step radical mechanism. (a) Draw the structure of the major product when NBS reacts with the following alkene. (b) Draw out the step-by-step mechanism to show how the reaction proceeds.CCI4NBS(18 pts) Draw a valid structure that contains one 3° alcohol, one 3° amine, one 1° halide, a sec-butyl functional group, an ether functional group, and only one chiral carbon. (b) Name the structure
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