Modeling the oxyethylation of primary aliphatic alcohols by ethylene oxide
โ Scribed by Yu. D. Panaev; I. E. Latyshev; S. A. Ternovskii
- Publisher
- Springer
- Year
- 1985
- Tongue
- English
- Weight
- 245 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0009-2355
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๐ SIMILAR VOLUMES
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
## Abstract The reaction constants for the oxidations of primary aliphatic alcohols with 12 dichromates and halochromates of heterocyclic bases do not differ significantly indicating operation of a common mechanism. ยฉ 2004 Wiley Periodicals, Inc. Int J Chem Kinet 37: 5โ9, 2005
1V.C.r (C;waf Ilritniu) (Iicccivcd Jum qth. 1961) The osidation of primary aliphatic alcoliols is customarily rcprcscntcd by the ccluations ant1 tllesc form tllc basis of an analJ\*tical method for the rlctcrminntiorl of mcthnnol and ethanol'. The mc4hocl is simple to perform and has the advantage
Such streaming is believed to be the cause of i v maxima observed earlier with acidified alcohol aqueous solutions when hydronium ion reduction is partly diffusion controlled 2. \* If the system is linear the increase in current is not dependent on the steady component of the light.