H. - •Br: Br: Allylic bromination of alkenes is accomplished with the reagent NBS (W-bromosuccinimide). The reaction proceeds by a radical chain mechanism. For the following reaction: NBS light, CCl4 -Br

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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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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.

H.
-
•Br:
Br:
Transcribed Image Text:H. - •Br: Br:
Allylic bromination of alkenes is accomplished with the reagent NBS (W-bromosuccinimide). The reaction proceeds by a radical chain mechanism.
For the following reaction:
NBS
light, CCl4
-Br
Transcribed Image Text:Allylic bromination of alkenes is accomplished with the reagent NBS (W-bromosuccinimide). The reaction proceeds by a radical chain mechanism. For the following reaction: NBS light, CCl4 -Br
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