Inner-square mechanism of oxidation. II. Stoichiometry and kinetics of the manganese(III) oxidation of thiocyanate, thiourea, and some alkylthioureas in acid perchlorate solution

1972 ◽  
Vol 11 (10) ◽  
pp. 2488-2494 ◽  
Author(s):  
Geoffrey. Davies
1991 ◽  
Vol 69 (12) ◽  
pp. 2018-2023 ◽  
Author(s):  
Refat M. Hassan

The kinetics of permanganate oxidation of DL-α-alanine in aqueous perchloric acid solution at a constant ionic strength of 2.0 mol dm−3 has been investigated spectrophotometrically. The reaction was found to show second-order kinetics overall with respect to each of the reactants in the slow initial stage; the second-order kinetics are not, however, maintained throughout the relatively fast final stage of reaction. The added salts lead to the prediction that Mn(III) and (or) Mn(IV) play a very important role in the reaction kinetics. A tentative mechanism consistent with the kinetics is discussed. Key words: kinetics, oxidation, reduction, amino acids, permanganate.


1977 ◽  
Vol 8 (34) ◽  
pp. no-no
Author(s):  
R. A. RICKMAN ◽  
R. L. SORENSEN ◽  
K. O. WATKINS ◽  
G. DAVIES

1976 ◽  
Vol 29 (4) ◽  
pp. 915
Author(s):  
JD Edwards

The kinetics of the reduction of [(NH3)3Co,μ(NH2,0H,0H),Co(NH3)3]3+ by chromium(11) ion in aqueous perchlorate solution is reported. The results are interpreted in terms of a rapid pre-equilibrium involving hydrogen-ion catalysed hydroxo bridge cleavage, followed by rate determining inner-sphere reduction. A deprotonated aqua ligand is the bridge for electron transfer.


2010 ◽  
Vol 55 (28) ◽  
pp. 8416-8421 ◽  
Author(s):  
Lian Guo ◽  
Alexander Thompson ◽  
Peter C. Searson

1993 ◽  
Vol 58 (3) ◽  
pp. 538-546 ◽  
Author(s):  
Refat M. Hassan ◽  
Sahr A. El-Gaiar ◽  
Abd El-Hady M. El-Summan

The kinetics of permanganate oxidation of selenium dioxide in perchloric acid solutions at a constant ionic strength of 2.0 mol dm-3 has been investigated spectrophotometrically. A first-order reaction in [MnO4-] and fractional order with respect to selenium(IV) were observed. The reaction rate was found to be pH-independent at lower acid concentrations ([H+] < 0.5 mol dm-3) and was acid-catalyzed beyond this range. Addition of Mn2+ and F- ions leads to the prediction that MnO4- is the sole reactive species in the oxidation process. A tentative reaction mechanism consistent with the reaction kinetics has been proposed.


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