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.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter12: Chirality
Section: Chapter Questions
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The compound below is treated with N-
bromosuccinimide (NBS) in the
presence of light.
어
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. 어 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.
The compound below is treated with N-
(NBS) in the
bromosuccinimide
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- (NBS) in the bromosuccinimide 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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