Draw the possible products of this epoxide ring-openingreaction.Use a dash or wedge bond to indicate the stereochemistry ofsubstituents on asymmetric centers, where applicableIgnoreany inorganic byproducts.41100H1) NaOH / H₂O2) dilute HCI☑ⒸPlease select a drawing or reagent from the question area My1H1) NaOH/H₂O2) dilute HCISelect to Draw☑Please select a drawing or reagent from the question area

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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

Chapter16: Aldehydes And Ketones

Section: Chapter Questions

Problem 16.69P

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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

Draw the possible products of this epoxide ring-opening
reaction.
Use a dash or wedge bond to indicate the stereochemistry of
substituents on asymmetric centers, where applicableIgnore
any inorganic byproducts.
41100
H
1) NaOH / H₂O
2) dilute HCI
☑Ⓒ
Please select a drawing or reagent from the question area

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