9 1-Aminohexane yields 1-hexene under the following reaction conditions. Propose a structure for the intermediate and explain why it readily undergoes elimination using E2 mechanism. CH3(CH2)s-NH2 → (five-molar excess CH3CH2-Br/Silver oxide/H2O) → CH3(CH2)3-CH=CH2

Organic Chemistry
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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
Chapter18: Functional Derivatives Of Carboxylic Acids
Section: Chapter Questions
Problem 18.43P: The following sequence of steps converts (R)-2-octanol to (S)-2-octanol. Propose structural formulas...
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9. 1-Aminohexane yields 1-hexene under the following reaction conditions. Propose a
structure for the intermediate and explain why it readily undergoes elimination using E2
mechanism.
CH3(CH2)5-NH2 → (five-molar excess CH3CH2-Br/Silver oxide/H2O) → CH3(CH2)3-CH=CH2
Transcribed Image Text:9. 1-Aminohexane yields 1-hexene under the following reaction conditions. Propose a structure for the intermediate and explain why it readily undergoes elimination using E2 mechanism. CH3(CH2)5-NH2 → (five-molar excess CH3CH2-Br/Silver oxide/H2O) → CH3(CH2)3-CH=CH2
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