aprotic (solvent)

https://doi.org/10.1351/goldbook.A00425
[email protected]@ (in a given situation). (With extremely strong @[email protected] or @[email protected], solvents that are normally aprotic may accept or lose a @[email protected] For example, acetonitrile is in most instances an aprotic solvent, but it is @[email protected] in the presence of concentrated sulfuric acid and @[email protected] in the presence of potassium tert-butoxide. Similar considerations apply to benzene, trichloromethane, etc.)
See also:
dipolar aprotic solvent
Source:
PAC, 1994, 66, 1077. (Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994)) on page 1085 [Terms] [Paper]
Cite as: IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). Online version (2019-) created by S. J. Chalk. ISBN 0-9678550-9-8. https://doi.org/10.1351/goldbook.
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Last revised: February 24, 2014