A new second-order reaction kinetics equation

1987 ◽  
Vol 91 (12) ◽  
pp. 3117-3119 ◽  
Author(s):  
Malcolm. Dole
Keyword(s):  
Reaction Kinetics ◽  
Order Reaction ◽  
Second Order ◽  
Kinetics Equation ◽  
Second Order Reaction

Infrared spectrometry to study second order reaction kinetics

1964 ◽  
Vol 41 (11) ◽  
pp. 613
Author(s):  
B. Gastambide ◽  
J. Blanc ◽  
Y. Allamagny
Keyword(s):  
Reaction Kinetics ◽  
Order Reaction ◽  
Second Order ◽  
Infrared Spectrometry ◽  
Second Order Reaction

A two-phase second-order reaction: Kinetics of epoxidation of methyl 12,13-epoxyoleate

1969 ◽  
Vol 46 (6) ◽  
pp. 327-331 ◽  
Author(s):  
H. L. Rothbart ◽  
M. E. Snook ◽  
J. F. Rusling ◽  
W. E. Scott
Keyword(s):  
Reaction Kinetics ◽  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Two Phase ◽  
Kinetics Of

Stability of radical anions derived from substituted 5-nitrofurans investigated by ESR spectroscopy

1985 ◽  
Vol 50 (7) ◽  
pp. 1594-1601 ◽  
Author(s):  
Jiří Klíma ◽  
Larisa Baumane ◽  
Janis Stradinš ◽  
Jiří Volke ◽  
Romualds Gavars
Keyword(s):  
Radical Anion ◽  
High Stability ◽  
Esr Spectroscopy ◽  
Reaction Path ◽  
Order Reaction ◽  
Second Order ◽  
Radical Anions ◽  
Second Order Reaction ◽  
Unpaired Electron Density ◽  
The Stability

It has been found that the decay in dimethylformamide and dimethylformamide-water mixtures of radical anions in five of the investigated 5-nitrofurans is governed by a second-order reaction. Only the decay of the radical anion generated from 5-nitro-2-furfural III may be described by an equation including parallel first- and second-order reactions; this behaviour is evidently caused by the relatively high stability of the corresponding dianion, this being an intermediate in the reaction path. The presence of a larger conjugated system in the substituent in position 2 results in a decrease of the unpaired electron density in the nitro group and, consequently, an increase in the stability of the corresponding radical anions.

Kinetics of the reaction between hexamethylenediisocyanate and 1-pentanol

1983 ◽  
Vol 48 (11) ◽  
pp. 3279-3286
Author(s):  
Slavko Hudeček ◽  
Miloslav Bohdanecký ◽  
Ivana Hudečková ◽  
Pavel Špaček ◽  
Pavel Čefelín
Keyword(s):  
Liquid Chromatography ◽  
Rate Constants ◽  
Reversed Phase ◽  
Order Reaction ◽  
Second Order ◽  
Second Order Reaction ◽  
Reversed Phase Liquid Chromatography ◽  
Consecutive Reactions ◽  
Phase Liquid ◽  
Kinetics Of

The reaction between hexamethylenediisocyanate and 1-pentanol in toluene was studied by means of reversed-phase liquid chromatography. By employing this method, it was possible to determine all components of the reaction mixture including both products, i.e. N-(6-isocyanate hexyl)pentylcarbamate and N,N'-bis(pentyloxycarbonyl)hexamethylenediamine. Relations for the calculation of kinetic constants were derived assuming a competitive consecutive second-order reaction. It was demonstrated that the reaction involved in this case is indeed a second-order reaction, and the rate constants of the first and second consecutive reactions were determined.

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