In alkaline media the 2-, 3-, and Cmonohexanoates of lincomycin rapidly isomerize, each entering into facile equilibrium with the other two, accompanied by hydrolysis of each species to lincomycin. The concentration-time curves of the three esters and of lincomycin as observed in a single experiment
Kinetics of the acid and alkaline hydrolysis of Monofluorophosphite
β Scribed by Karla Dishman; Leigh Ann Karnell; John W. Larson
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 280 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The kinetics of the acid and alkaline hydrolysis of monoflorophosphorous acid has been studied by P-31 NMR and static pH titration over a wide temperature range. The acid catalyzed hydrolysis has a rate constant at 25Β°C equal to 0.35 dm3 mol-l s-l and an activation energy of 53 k J while the alkaline hydrolysis has a rate constant of 4.6 dm3 mol-' s-l and an activation energy of 42 kJ. When the hydrogen in this compound is replaced by either fluorine or a hydroxyl group, the rates of reaction decrease by two orders of magnitude.
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