𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mechanism of the acid catalysed hydrolysis of the chromatopenta-amminecobalt(III) ion

✍ Scribed by Novelette P. Sadler; Tara P. Dasgupta

Publisher
Springer
Year
1992
Tongue
English
Weight
365 KB
Volume
17
Category
Article
ISSN
0340-4285

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Kinetics and mechanism of the acid-catal
Kinetics and mechanism of the acid-catalysed hydrolysis of the carbonatotetraimidazolecobalt(III) ion
✍ Eleonora Danilczuk; Janusz ChatΕ‚as πŸ“‚ Article πŸ“… 1996 πŸ› Springer 🌐 English βš– 431 KB

The kinetics of the acid-catalysed hydrolysis of the [(imidazole)4Co(CO3) ] + ion was found to follow the rate law -dln[complex]/dt = k~K[H+]/(1 + K[H+]) in the 25-45 ~ range, [H +] 0.05-1.0 M range and I = 1.0 M. The reaction sequence consists of a rapid protonation equilibrium followed by the one-

The acid catalysed hydrolysis of N-acety
The acid catalysed hydrolysis of N-acetylsulphanilic acid - a changing mechanism.
✍ J.W. Barnett; Charmian J. O'Connor πŸ“‚ Article πŸ“… 1971 πŸ› Elsevier Science 🌐 French βš– 111 KB

We recently reported' that acctanilide readily sulphonatcs in solutions of sulphuric acid > 70 per cent I& to form I+acetylsulphanilic acid , and noted that the rate of hydrolysis of this latter compound increased with increasing acidity beyond 80 per cent d= sulphuric acid. Ve have now prepared IG

The Mechanism of the Acid-catalysed Hydr
The Mechanism of the Acid-catalysed Hydrolysis of 1-Aryl-2,2,2-trifluorodiazoethanes
✍ Georges Diderich πŸ“‚ Article πŸ“… 1972 πŸ› John Wiley and Sons 🌐 German βš– 569 KB

Szinzmavy. The rates of the acid-catalysetl hydrolysis < I f a serics of hryi-2,2,2-trifluorocliazocthanes Ia-d havc been mcasured in dioxan/\vatcr/HC104. Thc results arc well corrclatetl with the Hanznzett equation when up substituent constants are used ( @ = -1.74 and er, = -1.75). Kinetic solven

The acid-catalysed hydrolysis of ethylen
The acid-catalysed hydrolysis of ethylene episulphoxide
✍ G.E. Manser; A.D. Mesure; J.G. Tillett πŸ“‚ Article πŸ“… 1968 πŸ› Elsevier Science 🌐 French βš– 205 KB

The formation of episulphones fran the corresponding episulphides by oxidation with hydrogen peroxide is well docwnented (1). Only recently, however, has a successful partial oxidation procedure been reported (2) for the preparation of a number of episulphoxides.