Identify all resonance forms of the enolate formed, and indicate whether or not a substantial amount of starting ketone will be present together with the enolate at equilibrium. (select all that apply) O No, there will NOT be a substantial amount of diketone present after equilibrium has been established. J 0 ✔ Yes, there will be a substantial amount of diketone present after equilibrium has been established. >
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.
 alt="Identify all resonance forms of the enolate formed, and
indicate whether or not a substantial amount of starting
ketone will be present together with the enolate at
equilibrium. (select all that apply)
No, there will NOT be a substantial amount of
diketone present after equilibrium has been
established.
✔ Yes, there will be a substantial amount of diketone
present after equilibrium has been established.
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