Oxidation of l-rhamnose and d-mannose by chromium(VI) in aqueous acetic acid
β Scribed by M. Rizzotto; M.I. Frascaroli; S. Signorella; L.F. Sala
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 509 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0277-5387
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The hexacyanoferrate(II1)-thallium(1) reaction in aqueous acetic acid containing large concentrations of hydrochloric acid is considerably accelerated both by hydrogen and chloride ions as well as increasing acetic acid in the medium. The experimental results obey the rate law (1) where PI to p6 (1
The reaction between chromium(V1) and L-ascorbic acid has been studied by spectrophotometry in the presence of aqueous citrate buffers in the pH range 5.69-7.21. The reaction is slowed down by an increase of the ionic strength. At constant ionic strength, manganese(I1) ion does not exert any appreci
Kinetics of oxidation of L-aspartic acid and L-glutamic acid by manganese(II1) ions have been studied in aqueous sulphuric acid, acetic acid, and pyrophosphate media. Manganese(II1) solutions were prepared by known electrolytidchemical methods in the three media. The nature of the oxidizing species
Manganese(III) solutions were prepared by known electrochemical methods in sulfuric acid, acetic acid, and pyrophosphate media. The nature of the oxidizing species present in manganese(III) solutions was characterized by spectrophotometric and redox potential measurements. Kinetics of oxidation of L