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Acid catalysis of hydrolysis

The carboethoxy stabilized secondary enamines, 25 and 26, were studied by Guthrie and Jordan68. In the absence of buffer, and at pH 5 to 6, acid catalysis is evident and a solvent kinetic isotope effect, (kH+/kD+) = 2.3, is found for 25. These results clearly support rate-controlling C-protonation of the enamine the catalytic constants are included in Table 9. Both 25 and 26 show general-acid catalysis of hydrolysis in the pH... [Pg.1080]

Values for Acetic Acid Catalysis of Hydrolysis of Cyanoketen Dimethyl Acetal... [Pg.315]

See other pages where Acid catalysis of hydrolysis is mentioned: [Pg.315]   
See also in sourсe #XX -- [ Pg.92 , Pg.99 , Pg.105 ]

See also in sourсe #XX -- [ Pg.92 , Pg.99 , Pg.105 ]



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Acid catalysis hydrolysis

Acid catalysis of acetal formation and hydrolysis

Acid catalysis of acetal hydrolysis

Acid catalysis of amide hydrolysis

Acid catalysis of ester formation and hydrolysis

Acid catalysis of ester hydrolysis

Acid catalysis of glycoside hydrolysis

Acid catalysis of nitrile hydrolysis

Catalysis hydrolysis

Catalysis of hydrolysis

General acid catalysis in hydrolysis of enol ethers

Intermolecular General Acid Catalysis of Glycoside Hydrolysis

Intramolecular General Acid Catalysis of Glycoside Hydrolysis

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