[Review Topics] [References] Draw structural formulas for the diene and dienophile that combine in a Diels-Alder reaction to form the product shown. Diene + Dienophile CH3O CH₂ I wwwwwww
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.
![[Review Topics]
[References]
Draw structural formulas for the diene and dienophile that combine in a Diels-Alder reaction to form
the product shown.
Diene + Dienophile
CH3O
CH₂
I
wwwwwww](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F637a8243-98d2-45ca-8dd1-4e9d7d0f97ca%2F5745168d-06bc-4bb5-94b7-3face1d1b0d8%2F5hs5wfg.jpeg&w=3840&q=75)
-> The Diels Alder reaction is the reaction between a conjugated Diene and an alkene(dienophile) to form unsaturated six membered rings .
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