.Br CN HO, a-Determine if it will follow an SN1 or SN2 mechanism and state which it will follow. b-Explain the reasoning for the mechanism choice, including analysis of the alkyl halide, nucleophile and solvent. c-Draw the mechanism the reaction will follow.

.Br CN HO, a-Determine if it will follow an SN1 or SN2 mechanism and state which it will follow. b-Explain the reasoning for the mechanism choice, including analysis of the alkyl halide, nucleophile and solvent. c-Draw the mechanism the reaction will follow.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 26E

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Concept explainers

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.

Question

CN
HO
a-Determine if it will follow an SN1 or SN2 mechanism and state which it will follow.
b-Explain the reasoning for the mechanism choice, including analysis of the alkyl
halide, nucleophile and solvent.
c-Draw the mechanism the reaction will follow.

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