: ? H-C-I エーO-エ

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
Chapter11: Ethers, Epoxides, And Sulfides
Section: Chapter Questions
Problem 11.42P
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Updated ZRW: 1-20-14
Post lab Questions:
1. Considering the reaction you just ran, and assuming you've obtained a mixture of the
following compounds (rather than the desired product) in the organic layer after
performing the reaction. What experimental error could have led to these products?
H.
(1:1 mixture)
2. Propose a synthesis of the following molecule using benzene as your starting material:
H3C
OH
3. For the reaction you reformed, we quenched the reaction with ammonium chloride in
order to protonate the alkoxide ion generated from the reaction (below), What would our
product be if we instead added methyl iodide instead of ammonium chloride?
In your reaction:
OH
H-N-H CI
+ NH3
CI
The proposed reaction:
H-C-I
F.
Transcribed Image Text:Updated ZRW: 1-20-14 Post lab Questions: 1. Considering the reaction you just ran, and assuming you've obtained a mixture of the following compounds (rather than the desired product) in the organic layer after performing the reaction. What experimental error could have led to these products? H. (1:1 mixture) 2. Propose a synthesis of the following molecule using benzene as your starting material: H3C OH 3. For the reaction you reformed, we quenched the reaction with ammonium chloride in order to protonate the alkoxide ion generated from the reaction (below), What would our product be if we instead added methyl iodide instead of ammonium chloride? In your reaction: OH H-N-H CI + NH3 CI The proposed reaction: H-C-I F.
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