Allylic bromination of alkenes is accomplished with the reagent NBS (N-bromosuccinimide). The reaction proceeds by a radical chain mechanism. For the following reaction: NBS Br light, CCI4 a Select the species that you would expect to react in the first propagation step and draw curly arrows to show the mechanism. Use half-headed (fishhook) curved arrows to show electron reorganization. When drawing bond formation by pairing of single electrons, terminate the arrows in a hotspot located to one side of a reacting radical. This hotspot is not associated with any structural feature. Arrow-pushing Instructions 将一郎: H2 Proviouo

Chemistry
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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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Allylic bromination of alkenes is accomplished with the reagent NBS (N-bromosuccinimide).
The reaction proceeds by a radical chain mechanism.
For the following reaction:
NBS
Br
light, CCI4
a Select the species that you would expect to react in the first propagation step and draw
curly arrows to show the mechanism. Use half-headed (fishhook) curved arrows to show
electron reorganization.
When drawing bond formation by pairing of single electrons, terminate the arrows in a
hotspot located to one side of a reacting radical. This hotspot is not associated with any
structural feature.
Arrow-pushing Instructions
将一郎:
Br
H2
Previous
Next
Transcribed Image Text:Allylic bromination of alkenes is accomplished with the reagent NBS (N-bromosuccinimide). The reaction proceeds by a radical chain mechanism. For the following reaction: NBS Br light, CCI4 a Select the species that you would expect to react in the first propagation step and draw curly arrows to show the mechanism. Use half-headed (fishhook) curved arrows to show electron reorganization. When drawing bond formation by pairing of single electrons, terminate the arrows in a hotspot located to one side of a reacting radical. This hotspot is not associated with any structural feature. Arrow-pushing Instructions 将一郎: Br H2 Previous Next
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