Dimethyl sulfoxide is an important polar aprotic solvent that have the right to dissolve both polar and nonpolar compounds and is miscible in a wide range of organic solvents and also water since it penetrates the skin very readily, that is occasionally used as a vehicle for topical applications of pharmaceuticals. Draw the structure of dimethyl sulfoxide. Include any kind of nonbonding electrons on sulfur, and also minimize formal charges by allowing sulfur to expand its octet. Draw the necessary product that the following reaction between (1S,3S)-1-chloro-3-methylcyclopentane and also methanethiol in the presence of sodium hydroxide suspect the significant product for the following reaction. Attract an alcohol and an alkyl bromide that can be merged to provide the ether shown. Unsymmetrical ethers deserve to be made by the Williamson synthesis, in i beg your pardon an alkoxide ion reacts with an alkyl bromide. Draw the structure of the alkoxide and the alkyl bromide essential to create 2-ethoxy-2-methylpropane (a. K. A /-butyl ethyl ether), shown below. Display charges wherein appropriate.


You are watching: Draw an alcohol and an alkyl bromide that could be combined to give the ether shown.

present transcribed picture text Dimethyl sulfoxide is an essential polar aprotic solvent that have the right to dissolve both polar and nonpolar compounds and also is miscible in a wide selection of organic solvents and water since it penetrates the skin really readily, the is periodically used as a auto for topical application of pharmaceuticals. Draw the framework of dimethyl sulfoxide. Include any type of nonbonding electron on sulfur, and minimize official charges by allowing sulfur to expand its octet. Draw the organic product that the following reaction in between (1S,3S)-1-chloro-3-methylcyclopentane and methanethiol in the presence of sodium hydroxide suspect the major product because that the following reaction. Draw an alcohol and also an alkyl bromide that might be combined to give the ether shown. Unsymmetrical ethers can be make by the Williamson synthesis, in i m sorry an alkoxide ion reacts through an alkyl bromide. Attract the framework of the alkoxide and the alkyl bromide required to produce 2-ethoxy-2-methylpropane (a. K. A /-butyl ethyl ether), displayed below. Present charges whereby appropriate.

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Draw structure formulas for an aldehyde or ketone and also alkyl (or aryl) bromide that could be provided in a Grignard synthesis of the alcohol shown.

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Draw structural formulas because that an aldehyde or ketone and also alkyl (or aryl) bromide that can be provided in a Grignard synthetic of the alcohol shown.

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Unsymmetrical ethers can be made by the Williamson synthesis, in i m sorry an alkoxide ion reacts with an alkyl bromide. Attract the framework of the alkoxide and also the alkyl bromide essential to produce 2-ethoxy-2-methylpropane (a.k.a t-buty! ethyl ether). Displayed below. Show charges whereby appropriate.


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display transcribed photo text Unsymmetrical ethers deserve to be make by the Williamson synthesis, in i m sorry an alkoxide ion reacts with an alkyl bromide. Attract the framework of the alkoxide and the alkyl bromide necessary to develop 2-ethoxy-2-methylpropane (a.k.a t-buty! ethyl ether). Presented below. Show charges where appropriate.