Part I. Draw the complete, detailed mechanism (fishhook arrows) for the following reaction, showing molecul (1) being transformed into molecule (2). Only one termination step is required Initiation: Propagation: Cl₂ hu Termination: -CI llut not asigns brod homoo iw oxuduma snil-brod ni mwib od bluor (2) 03 9102 solamni 21 set poy belgeuz YARDIN al nexe gris Juodquod 92619 of uoy wolle liv میں Part II. For the following reaction, draw the complete, detailed mechanism (curved arrows) to show how en will be converted into aldehyde 2, using mechanistic skills gained in this course LiOH H₂O of H 2
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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