๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Kinetics and mechanism of oxidation of aliphatic primary alcohols by quinolinium bromochromate

โœ Scribed by Sonu Saraswat; Vinita Sharma; K. K. Banerji


Publisher
Indian Academy of Sciences,Royal Society of Chemistry
Year
2003
Tongue
English
Weight
48 KB
Volume
115
Category
Article
ISSN
0253-4134

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Kinetics and mechanism of the oxidation
โœ K. Choudhary; P. K. Sharma; K. K. Banerji ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 134 KB ๐Ÿ‘ 2 views

The oxidation of some aliphatic alcohols by quinolinium fluorochromate (QFC) in dimethyl sulfoxide leads to the formation of corresponding carbonyl compounds. The reaction is first order with respect to QFC. The reaction exhibited Michaelis-Menten type kinetics with respect to the alcohol. The react

Kinetics and mechanism of the oxidation
โœ P. Surya Chandra Rao; Deepa Suri; Seema Kothari; Kalyan K. Banerji ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 122 KB ๐Ÿ‘ 2 views

The kinetics of oxidation of four vicinal diols, four nonvicinal diols, and one of their monoethers by pyridinium bromochromate (PBC) have been studied in dimethyl sulfoxide. The main product of oxidation is the corresponding hydroxyaldehyde. The reaction is first-order with respect to each the diol

Kinetics and mechanism of the oxidation
โœ Suman Mittal; Vinita Sharma; Kalyan K. Banerji ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 423 KB

The oxidation of primary alcohols by sodium N-chloroethylcarbamate in acid solution, results in the formation of corresponding aldehydes. The reaction is first order with respect to the oxidant and alcohol. The rate increases with an increase in acidity. The oxidation of ap-dideuterioethanol exhibit

Kinetics and mechanism of oxidation of a
โœ Rajalingam Renganathan; Pichai Maruthamuthu ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 461 KB

The kinetics of the oxidation of aliphatic aldehydes, formaldehyde, acetaldehyde, propionaldehyde, n-butyraldehyde, and trichloroacetaldehyde by Peroxomonosulphate (PMS) was carried out in aqueous perchloric acid medium (0.1-1 M H+) a t constant ionic strength of 1.2 M in the temperature range 1O"-6