Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the missing reactants/intermediates in this E1 mechanism. Include all lone pairs. Ignore byproducts.Ignore stereochemistry. :OH H H₂O* heat Select to Draw I Intermediate dissociation

Q: Multiply 21.5 x 3.149 and report the answer to correct sigfigs. 67.704 6.83 67.7 0 67 70

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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.