23. Given the following structures, which of the statements below is incorrect? Br (1) Br Br (III) A) Reaction of III with water will produce an alcohol via an SNl mechanism. B) Reaction of I with OH will produce an alcohol via an SN2 mechanism. C) Molecule II can react with some nucleophiles via an SN2 mechanism. D) When II undergoes a successful substitution reaction with CH3COONa (where CHICOO is a nucleophile) the product is an ester. E) Molecule I will react with nucleophiles via a two-step substitution mechanism.
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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