Question

the following alkene is treated with one equivalent of n-bromosuccinimide in dichloromethane in the presence of light to give bromination product(s). draw a line-angle formula for each product formed. you do not have to consider stereochemistry. draw organic products only. draw one structure per sketcher. add additional sketchers using the drop-down menu in the bottom right corner. separate multiple products using the sign from the drop-down menu.

Answer 1

karl Ziegler reported that alkenes react with N- bromo succinamide in the presence of light to give products resulting from substitution of hydrogen by bromine at the allylic  .

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