The compound below is treated with N-bromosuccinimide (NBS) in t presence of light. Draw both resonance structures for the radical produced by reaction o 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 č down menu. • Include all valence radical electrons in your answer.

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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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 drop-
down menu.
• Include all valence radical electrons in your answer.
Transcribed Image Text: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 drop- down menu. • Include all valence radical electrons in your answer.
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