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

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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
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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