scholarly journals Kinetics of Oxidation of Amino Acids by Chloramine-T. A Reinvestigation on the Oxidation of Alanine, 2-Aminobutyric Acid, Valine, Serine, and Threonine

1987 ◽  
Vol 60 (9) ◽  
pp. 3397-3404 ◽  
Author(s):  
M. Shanmugam Ramachandran ◽  
T. Subburamiyer Vivekanandam
Keyword(s):  
Amino Acids ◽  
Aminobutyric Acid ◽  
Kinetics Of Oxidation ◽  
Chloramine T ◽  
Kinetics Of

Kinetics of oxidation of amino acids by chloramine T. A reinvestigation

1985 ◽  
pp. 1507 ◽  
Author(s):  
M. Shanmugam Ramachandran ◽  
T. Subburamiyer Vivekanandam ◽  
Rajarathinam Nithyanandhan
Keyword(s):  
Amino Acids ◽  
Kinetics Of Oxidation ◽  
Chloramine T ◽  
Kinetics Of

Kinetics of oxidation of amino acids by alkaline hexacyanoferrate(III)

1990 ◽  
Vol 3 (12) ◽  
pp. 799-802 ◽  
Author(s):  
Didcy Laloo ◽  
Mahendra K. Mahanti
Keyword(s):  
Amino Acids ◽  
Kinetics Of Oxidation ◽  
Kinetics Of

A Study of Substituent Effect on the Oxidative Strengths of N-Chloroarenesulphonamides: Kinetics of Oxidation of Leucine and Isoleucine in Aqueous Acid Medium

2004 ◽  
Vol 59 (1) ◽  
pp. 63-72 ◽  
Author(s):  
Mahesha Shetty ◽  
B. Thimme Gowda
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Ionic Strength ◽  
Acid Medium ◽  
Benzene Ring ◽  
Thermodynamic Data ◽  
Substituent Effect ◽  
Kinetics Of Oxidation ◽  
Aqueous Acid ◽  
Kinetics Of

Abstract To study the variation of oxidative strengths of N-chloro-arenesulphonamides with substitution in the benzene ring, six mono- and five di-substituted N-chloro-arenesulphonamides are employed as oxidants for studying the kinetics of oxidation of two neutral amino acids, L-leucine and Lisoleucine in aqueous acid medium. The N-chloro-arenesulphonamides studied are of the constitution: ArSO2NaNCl·H2O (where Ar = C6H5, 4-CH3C6H4, 4-C2H5C6H4, 4-FC6H4, 4-ClC6H4, 4-BrC6H4, 2,3-(CH3)2C6H3, 2,4-(CH3)2C6H3, 2-CH3-4-ClC6H3, 2,4-Cl2C6H3, and 3,4-Cl2C6H3). The reactions show second order kinetics in [oxidant], fractional order in [amino acid] and inverse dependence on [H+]. Addition of the reduced product of the oxidants or variation in ionic strength of the medium has no significant effect on the rates of oxidations. A two-pathway mechanism is considered to explain the experimental results. Effective oxidizing species of the oxidants is Cl+ in different forms. Therefore the oxidising strengths of N-chloro-arenesulphonamides depend on the ease with which Cl+ is released from them. The study reveals that the introduction of substituent in the benzene ring of the oxidant affects both the kinetic and thermodynamic data for the oxidations The electron releasing groups such as CH3 generally inhibit the rates, while electron-withdrawing groups such as Cl enhance this ability, as the electron withdrawing groups ease the release of Cl+ from the reagents and hence increase the oxidising strengths. The on Ea and logA and validity of the Hammett and isokinetic relationships for the oxidations are also analysed.

scholarly journals Kinetics of Oxidation of Some Amino Acids by N-Chlorosaccharin in Aqueous Acetic Acid Medium

2004 ◽  
Vol 1 (2) ◽  
pp. 127-131 ◽  
Author(s):  
N. A. Mohamed Farook ◽  
R. Prabaharan ◽  
S. Rahini ◽  
R. Senthil Kumar ◽  
G. Rajamahendran ◽  
...  
Keyword(s):  
Amino Acids ◽  
Acetic Acid ◽  
Acid Medium ◽  
Hypochlorous Acid ◽  
Activation Parameters ◽  
Slow Step ◽  
Aqueous Acetic Acid ◽  
Acetic Acid Medium ◽  
Kinetics Of Oxidation ◽  
Kinetics Of

The kinetics of oxidation of some amino acids namely, glycine, alanine, aspartic acid, arginine, and histidine, (AA) byN-chlorosaccharin (NCSA) in aqueous acetic acid medium in the presence of perchloric acid have been investigated. The observed rate of oxidation is first order in [AA], [NCSA] and of inverse fractional order in [H+]. The main product of the oxidation is the corresponding aldehyde. The ionic strength on the reaction rate has no significant effect. The effect of changing the dielectric constant of the medium on the rate indicates the reaction to be of dipole-dipole type. Hypochlorous acid has been postulated as the reactive oxidizing species. The reaction constants involved in the mechanism are derived. The activation parameters are computed with respect to slow step of the mechanism.

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