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 CH;CH2-Br/Silver oxide/H2O) → CH:(CH2)3-CH=CH2

Organic Chemistry
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ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter27: Biomolecules: Lipids
Section27.SE: Something Extra
Problem 47AP: Cembrene, C20H32, is a diterpenoid hydrocarbon isolated from pine resin. Cembrene has a UV...
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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)s-NH2 > (five-molar excess CH;CH2-Br/Silver oxide/H2O) → CH:(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)s-NH2 > (five-molar excess CH;CH2-Br/Silver oxide/H2O) → CH:(CH2)3-CH=CH2
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