QUESTION 48 In the mechanism of an acid catalyzed nucleophilic substitution of an alcohol with a halide, which best describes the first step of the mec The halide acts as an electrophile and is attacked by the C attached to the - OH. The H of acid acts as a nucleophile and attacks the O of the alcohol. The halide acts as a nucleophile and attacks the C attached to the - OH. The Hof acid acts as an electrophile and is attacked by the O of the alcohol.
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.
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