15 EtgSiOTf (16) CH;CN OTf EtO EtO Show the mechanism for this reaction

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Q: specific absorbance ratio

A: A1=€1cl and A2=€2cl    A1/A2=€1/€2

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Q: Ô https://app.101edu.co Question 3 of 24 A substance which is cyclic, conjugated, and has 4n + 2 pi ...

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A:                                       Volume of tank = 75.0 L               Initial number of moles ...

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A: Equilibrium constant K = [P]÷[R] [P] = concentration of product  [R] = concentration of reactant

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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.