1. Which alkyl bromide is the best choice to use as a reagent in a Williamson ether synthesis of 2-propoxybutane? OCH₂ C 2. What is the product of this alkoxymercuration-demercuration reaction? 1. Hg(OAc)₂. CH₂OH 2. NaBH₂ H₂CO D H₂CO
1. Which alkyl bromide is the best choice to use as a reagent in a Williamson ether synthesis of 2-propoxybutane? OCH₂ C 2. What is the product of this alkoxymercuration-demercuration reaction? 1. Hg(OAc)₂. CH₂OH 2. NaBH₂ H₂CO D H₂CO
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:1. Which alkyl bromide is the best choice to use as a reagent in a Williamson ether synthesis
of 2-propoxybutane?
A
Br
A
B
OCH3
2. What is the product of this alkoxymercuration-demercuration reaction?
B
OCH₂
C
H₂CO
Br
1. Hg(OAc)2, CH3OH
2. NaBH4
C
HyCO.
D
D
Expert Solution

Overview
The Williamson ether synthesis is a chemical reaction that involves the formation of an ether by the reaction of an alkoxide ion with a primary alkyl halide or tosylate.
The mercuration-demercuration reaction is a chemical reaction that involves the addition of a mercuric ion (Hg2+) to an alkene, followed by the reduction of the resulting mercurinium ion intermediate to yield an alcohol.
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