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 othe 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.000Previous

Answer image:When the given compound is treated with N-bromosuccinimide (NBS) in the presence of…

Answered: The compound below is treated with…

Pushing Electrons

4th Edition

ISBN:9781133951889

Author:Weeks, Daniel P.

Publisher:Weeks, Daniel P.

Chapter2: Resonance Structures

Section: Chapter Questions

Problem 6EQ: Pairs of unshared electrons can be pushed. One Lewis structure for the methoxy-methyl cation is ....

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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 С-Н bond.
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Pairs of unshared electrons can be pushed. One Lewis structure for the methoxy-methyl cation is . The structure contains a pair of pushable electrons, namely, the unshared electrons on the atom. The structure also contains a positively charged atom that can act as a . A second resonance structure can be generated by pushing the unshared electrons to the receptor. Thus, It is not possible to push electrons toward the other carbon, because it is not a receptor. If you tried to push electrons to this carbon, you would generate a pentavalent carbon, which is not possible.

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