Definitions

1. In aprotic solvents, the rate-controlling stage of the reaction is obviously the nucleophilic attack of the amine at the carbonyl carbon of the ring. (Web site)

Dimer

1. In aprotic solvents, oligomers, such as the well-known acetic acid dimer, may be formed by hydrogen bonding. (Web site)

Protic Solvents

1. The Bamford-Stevens reaction gives carbenes in aprotic solvents and carbenium ions in protic solvents. (Web site)

Protic Solvent

1. The usage of aprotic solvents gives predominantly Z- alkenes, while protic solvent gives a mixture of E- and Z-alkenes. (Web site)

Polar

1. Acetone, methyl ethyl ketone, ethyl acetate, acetonitrile and other polar aprotic solvents are strong inducers of aneuploidy in Saccharomyces cerevisiae. (Web site)
2. Other polar aprotic solvents (hexamethylphosphoric triamide, dimethyl sulfoxide, N -methylpyrrolidone) have been used.
3. Polar, aprotic solvents as a class are well known to those skilled in organic chemistry. (Web site)

Protic

1. Subsequent reaction with protic or aprotic solvents strongly influences the outcome of the reaction.

Solvent

1. A solvent, if used, is preferably anhydrous, with aprotic solvents such as benzene and toluene being preferred.

Aprotic Solvents

1. Aprotic solvents may also be used, for example, dimethylformamide, dimethylacetamide, acetonitrile, and dimethyl sulfoxide. (Web site)
2. To achieve the condensation, the chemist should employ aprotic solvents with a high boiling point, such as benzene and toluene. (Web site)
3. To achieve the condensation, chemists should employ aprotic solvents with a high boiling point, such as benzene and toluene. (Web site)

Categories

1. Dimethyl Sulfoxide
2. Protic Solvent
3. High Boiling Point
4. Dimethylacetamide
5. Dimethylformamide
6. Books about "Aprotic Solvents" in Amazon.com
   

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