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.
![R
OH
R = H, alkyl, aryl
R₁
H
excess
R' = alkyl, aryl
H₂SO4
microwave
R
R'](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F104d41eb-f02b-4e6d-903d-dd6e6944a268%2F6ea5a39e-da4d-4e98-b75a-096b9853fb89%2F7xebee3_processed.jpeg&w=3840&q=75)
![Provide the complete arrow pushing mechanism for this transformation. You should use R
on your carboxylic acid to represent the carbon substituent. You can abbreviate the acid as
H-A but you must show appropriate charges when needed.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F104d41eb-f02b-4e6d-903d-dd6e6944a268%2F6ea5a39e-da4d-4e98-b75a-096b9853fb89%2Fnvm4ifd_processed.jpeg&w=3840&q=75)
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