1
answer
0
watching
298
views
6 Nov 2019
1.
2.
3.
Dimethyl sulfoxide is an important polar aprotic solvent that can dissolve both polar and nonpolar compounds and is miscible in a wide range of organic solvents as well as water Because it penetrates the skin very readily, it is sometimes used as a vehicle for topical application of pharmaceuticals. Draw the structure of dimethyl sulfoxide. Include any nonbonding electrons on sulfur, and minimize formal charges by allowing sulfur to expand its octet. Draw the organic product of the following reaction between (1S,3S)-1-chloro-3-methylcyclopentane and methanethiol in the presence of sodium hydroxide Predict the major product for the following reaction. Draw an alcohol and an alkyl bromide that could be combined to give the ether shown. Unsymmetrical ethers can be made by the Williamson synthesis, in which an alkoxide ion reacts with an alkyl bromide. Draw the structure of the alkoxide and the alkyl bromide needed to produce 2-ethoxy-2-methylpropane (a. k. a /-butyl ethyl ether), shown below. Show charges where appropriate. Show transcribed image text
1.
2.
3.
Dimethyl sulfoxide is an important polar aprotic solvent that can dissolve both polar and nonpolar compounds and is miscible in a wide range of organic solvents as well as water Because it penetrates the skin very readily, it is sometimes used as a vehicle for topical application of pharmaceuticals. Draw the structure of dimethyl sulfoxide. Include any nonbonding electrons on sulfur, and minimize formal charges by allowing sulfur to expand its octet. Draw the organic product of the following reaction between (1S,3S)-1-chloro-3-methylcyclopentane and methanethiol in the presence of sodium hydroxide Predict the major product for the following reaction. Draw an alcohol and an alkyl bromide that could be combined to give the ether shown. Unsymmetrical ethers can be made by the Williamson synthesis, in which an alkoxide ion reacts with an alkyl bromide. Draw the structure of the alkoxide and the alkyl bromide needed to produce 2-ethoxy-2-methylpropane (a. k. a /-butyl ethyl ether), shown below. Show charges where appropriate.
Show transcribed image text Trinidad TremblayLv2
21 Apr 2020