Using NBS will add a Br to the alkene via allylic radical bromination.
The compound below is treated with N-bromosuccinimide (NBS) in the presence of light.
Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs only at the weakest C-H bond.
You do not have to consider stereochemistry.
You do not have to explicitly draw H atoms.
Separate resonance structures using the ? symbol from the dropdown menu.
Include all valence radical electrons in your answer.
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