#9 please 7. Propose a mechanism for the synthesis of 2-methyl, 2-butanol from 2-chloro-2-methylbutane using water and heat (60°C).8. Explain why propanoic acid has a higher Ka than n-propanol, using resonance, particularlywhen the acidic proton is removed by NAOH.9. The reaction of 1-bromoheptane with the propionate anion to give heptyl propionate esteris greatly accelerated by adding catalytic amounts of KI. Explain.10 Evelee 1 othy1 2 jedocyclohevane vields the non Zaitsey eliminationoduot

Answered: Image /qna-images/answer/574969df-8b3b-468b-98aa-02236480ee21.jpg

Answered: . The reaction of 1-bromoheptane with…

. The reaction of 1-bromoheptane with the propionate anion to give heptyl propionate ester is greatly accelerated by adding catalytic amounts of KI. Explain.

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

Chapter19: Enolate Anions And Enamines

Section19.9: Crossed Enolate Reactions Using Lda

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Question

#9 please

7. Propose a mechanism for the synthesis of 2-methyl, 2-butanol from 2-chloro-2-
methylbutane using water and heat (60°C).
8. Explain why propanoic acid has a higher Ka than n-propanol, using resonance, particularly
when the acidic proton is removed by NAOH.
9. The reaction of 1-bromoheptane with the propionate anion to give heptyl propionate ester
is greatly accelerated by adding catalytic amounts of KI. Explain.
10 Evele
e 1 othy1 2 jedocyclohevane vields the non Zaitsey elimination
oduot

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