28. The following compounds undergo electrophilic aromatic substitution EXCEPT A. I and II B. III and IV C. II and III D. III I. II. 29. Which alkene is the most stable? A. I B. II C. III D. IV III. II. III. IV. N.X IV. 30. In the hydrohalogenation reaction of 1-phenylpropene, only 1-chloro-1-phenylpropane is obtained because A. a more stable carbonium ion is generated from this product. B. a more stable radical intermediate is generated from this product. C. a more stable benzene ring is generated from this product. D. a less stable transition state is generated from this product.
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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