7.37 Which product (or products) would you expect to obtain from each of the following reactions? In each part give the mechanism (SN1, SN2, E1, or E2) by which each product is formed and predict the relative amount of each product (i.e., would the product be the only product, the major product, a minor product, etc.?). Br EtO Meo (a) ELOH, 50 °C (g) 3-Chloropentane МеОН, 50 °С Br t-BUOK CH;CO2 (b) t-BUOH, 50 °C (h) 3-Chloropentane CHCO2Н, 50 °с Meo (c) HO Br МеОН, 50 °C (i) (R)-2-bromobutane 25 °C (d) t-BUOK 25 °C t-BUOH, 50 °C Br (j) (S)-3-Bromo-3-methylhexane MeOH (k) (S)-2-Bromooctane (e) t-Bu. МеОн, 50 °С acetone, 50 °C (1) (f) + NEC+ X→ Br + Br+ t-Bu, CN МеОН, 25 °С

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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.