Complete the curved arrow mechanisms for the following Diels Alder reactions. Pay careful attention to the stereochemistry and regiochemistry of the substituents! H₂CO OH

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Q: 3. CH₂OH For each of the following, indicate whether the carbon in red is chiral or achiral. Cl…

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Q: 3. Give the IUPAC name for the following: CH3 I O=C - CH3 -CH-CH₂-C-H

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Q: Draw the condensed structural formula of ethyl methyl ether.

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Q: A 5.71 g sample of an unknown salt (MM = 116.82 g/mol) is dissolved in 150.00 g water in a coffee…

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Q: нахон CI (1 eq) pyridine

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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.