Study of the mechanism of the oscillating reaction between bromate and phenol

1982 ◽  
Vol 47 (9) ◽  
pp. 2454-2465 ◽  
Author(s):  
Antonín Tockstein ◽  
Marie Handlířová

In the oscillating reaction of bromate with phenol in the medium of 0.4M-H2SO4, the length of the induction period is governed by a kinetic equation for a second-order reaction with a stoichiometry 1 : 1. The concentration of quinones in the reaction mixture increases also according to a kinetic equation for a second-order reaction. The influence of various compounds is discussed, whose additions shorten or prolong the induction period, bring about oscillations in a nonoscillating reaction mixture, or change the frequency of these oscillations. From the comparison of the time dependences of the potential of a platinum and an ion-selective electrodes and of the limiting current of the quinones, a reaction mechanism was proposed.

2003 ◽  
Vol 35 (6) ◽  
pp. 246-251
Author(s):  
A. E. Croce ◽  
L. V. Mogni ◽  
C. Vicente Irrazábal

2014 ◽  
Vol 68 (2) ◽  
Author(s):  
Zhi Hou ◽  
Li Luo ◽  
Chun Liu ◽  
Yuan Wang ◽  
Li Dai

AbstractThe reaction between caprolactam and ethanol was performed in near-critical water. The primary product (ethyl-6-aminohexanoate) was identified by GC-MS. The influences of the reaction temperature, residence time, initial ratio (reactant/water), pH, and additives on the yields of ethyl-6-aminohexanoate are discussed. The results showed that the yield of ethyl-6-aminohexanoate could be as high as 98 % with SnCl2 as an additive in near-critical water. At the same time, the reaction between caprolactam and ethanol was estimated by a lumped kinetic equation as a second-order reaction in near-critical water, and the activation energy was evaluated according to the Arrhenius equation under acidic and basic conditions. Based on the results, the reaction mechanism between caprolactam and ethanol in near-critical water is proposed.


1985 ◽  
Vol 50 (7) ◽  
pp. 1594-1601 ◽  
Author(s):  
Jiří Klíma ◽  
Larisa Baumane ◽  
Janis Stradinš ◽  
Jiří Volke ◽  
Romualds Gavars

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.


1983 ◽  
Vol 48 (11) ◽  
pp. 3279-3286
Author(s):  
Slavko Hudeček ◽  
Miloslav Bohdanecký ◽  
Ivana Hudečková ◽  
Pavel Špaček ◽  
Pavel Čefelín

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.


1973 ◽  
Vol 135 (3) ◽  
pp. 573-576 ◽  
Author(s):  
Bryan D. Young ◽  
John Paul

Certain features of RNA–DNA hybridization can be accounted for in terms of second-order-reaction theory. These include the use of annealing kinetics to estimate RNA complexity and the occurrence of approximately linear double-reciprocal plots.


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