Question 29 of 30 © Macmillan Learning > Bromination of an alkene by N-bromosuccinimide (NBS) in the presence of light or peroxide is a radical reaction and produces an allylic bromide. For the given bromination of 3-methylcyclopentene, select the allylic bromides from the set at the right that would be products of the reaction. CH3 8 NBS hv or ROOR Br A CH 3 CH₂ B Br Br CH3 C CH3 Br- CH3 CH3 CH₂ Br $ $ $ F G E Br Br

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Chapter1: Chemical Foundations
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Question 29 of 30 >
O Macmillan Learning
Bromination of an alkene by N-bromosuccinimide (NBS) in the presence of light or peroxide is a radical reaction and produces
an allylic bromide. For the given bromination of 3-methylcyclopentene, select the allylic bromides from the set at the right that
would be products of the reaction.
CH3
CH3
CH3
Br
CH3
CH₂
NBS
Br
Br
& = 8 &- $ $
hv or
ROOR
C
D
A
B
Br
Br-
CH3
E
CH3
F
Br
Br-
CH₂
G
Transcribed Image Text:Question 29 of 30 > O Macmillan Learning Bromination of an alkene by N-bromosuccinimide (NBS) in the presence of light or peroxide is a radical reaction and produces an allylic bromide. For the given bromination of 3-methylcyclopentene, select the allylic bromides from the set at the right that would be products of the reaction. CH3 CH3 CH3 Br CH3 CH₂ NBS Br Br & = 8 &- $ $ hv or ROOR C D A B Br Br- CH3 E CH3 F Br Br- CH₂ G
Question 29 of 30
O Macmillan Learning
>
G
B
C
E
D
hv or
ROOR
A
A
Which structures are products of this reaction?
Br-
CH3
E
B
Br
CH3
F
Br
C
Br
CH₂
G
D
Transcribed Image Text:Question 29 of 30 O Macmillan Learning > G B C E D hv or ROOR A A Which structures are products of this reaction? Br- CH3 E B Br CH3 F Br C Br CH₂ G D
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