What is the best reason to explain why the reaction below does not work aswritten?CIOHNaNH2O The secondary alkyl halide will give the elimination productO Ethanol is not reactive in this reactionO Chlorine is a poor leaving groupO Actually, it does work as writtenO NH2 is not a strong base

The first step is the formation of sodium ethoxide which then react with secondary halide giving the…

What is the best reason to explain why the reaction below does not work as written? CI NaNH2 HO O The secondary alkyl halide will give the elimination product Ethanol is not reactive in this reaction O Chlorine is a poor leaving group Actually, it does work as written O NH2 is not a strong base

What is the best reason to explain why the reaction below does not work as written? CI NaNH2 HO O The secondary alkyl halide will give the elimination product Ethanol is not reactive in this reaction O Chlorine is a poor leaving group Actually, it does work as written O NH2 is not a strong base

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.28P

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Question

What is the best reason to explain why the reaction below does not work as
written?
CI
OH
NaNH2
O The secondary alkyl halide will give the elimination product
O Ethanol is not reactive in this reaction
O Chlorine is a poor leaving group
O Actually, it does work as written
O NH2 is not a strong base

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