Hydrogen atom abstraction by a bromine radical in bromination of an alkane would be fastest with?

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Hydrogen atom abstraction by a bromine radical in bromination of an alkane would be fastest with?

Hydrogen atom abstraction by a bromine radical in bromination of an alkane would be fastest with
a primary C-H bond
a secondary C-H bond
a tertiary C-H bond
a Csp2-H bond
1. Which compound below is an allylic bromide?
A)
B)
A)
B)
C)
D)
Br
Br
2. Which is the best leaving group?
A) T
B)
3. An SN1 reaction
A) proceeds through carbocation intermediates
B) has a rate that only depends on the concentration of the substrate
C) always forms a mixture of enantiomers
D) occurs most readily using light (hv) and peroxides
Br
D)
D) Br
ted
Br
Transcribed Image Text:Hydrogen atom abstraction by a bromine radical in bromination of an alkane would be fastest with a primary C-H bond a secondary C-H bond a tertiary C-H bond a Csp2-H bond 1. Which compound below is an allylic bromide? A) B) A) B) C) D) Br Br 2. Which is the best leaving group? A) T B) 3. An SN1 reaction A) proceeds through carbocation intermediates B) has a rate that only depends on the concentration of the substrate C) always forms a mixture of enantiomers D) occurs most readily using light (hv) and peroxides Br D) D) Br ted Br
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