3) Complete the following reaction OH A) B) OH Br Br₂, H₂O OH | CH3 OH H OH OH CH3 11H Br Name 3 different reagents that can be used to do this conversion IIIOMS Also, show the reaction mechanism for the alcohol with one of the reagents you identified ICN

Q: rat CH3 CH3 - C - CI CH3 CH3 - CH3 — C — СІ CH3 OR + CH3 CH₂- О C он CACO H 0: CHICOH

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Q: Which one of the following is the general form of the Lewis dot formula for chlorine? :x:

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Q: Calculate the pH of solution where [H] = 0.000023

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Q: ОН Н H2N 5 - 10 min 22 °C ОН Н H2O

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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.