Kinetics of oxidation of heterocyclic secondary alcohols byN-chloro-r-2,c-6-diphenyl-t-3 methyl piperidin-4-one (NCP) in perchloric acid medium

1994 ◽  
Vol 26 (8) ◽  
pp. 847-855 ◽  
Author(s):  
Kuppusamy Selvaraj ◽  
Vinayagam Venkateswaran ◽  
Krishnasamy Ramarajan
Tetrahedron ◽  
1985 ◽  
Vol 41 (1) ◽  
pp. 205-208 ◽  
Author(s):  
Kalyan Kali Sengupta ◽  
Tapashi Samanta ◽  
Samarendra Nath Basu

2011 ◽  
Vol 8 (4) ◽  
pp. 1728-1733 ◽  
Author(s):  
N. M. I. Alhaji ◽  
S. Sofiya Lawrence Mary

The kinetics of oxidation of isoleucine withN-bromophthalimide has been studied in perchloric acid medium potentiometrically. The reaction is of first order each in [NBP] and [amino acid] and negative fractional order in [H+]. The rate is decreased by the addition of phthalimide. A decrease in the dielectric constant of the medium increases the rate. Addition of halide ions or acrylonitrile has no effect on the kinetics. Similarly, variation of ionic strength of the medium does not affect the reaction rate. The reaction rate has been determined at different temperatures and activation parameters have been calculated. A suitable mechanism involving hypobromous acid as reactive species has been proposed.


2021 ◽  
Vol 75 ◽  
Author(s):  
Mohammed Hassan ◽  
Mohammad Al-Dhoun ◽  
Yazan Batineh ◽  
Ahmad A. Najjar ◽  
Adnan Dahadha ◽  
...  

1989 ◽  
Vol 38 (2) ◽  
pp. 313-318 ◽  
Author(s):  
Kalyan Kali Sen Gupta ◽  
Mrityunjoy Adhikari ◽  
Shipra Sen Gupta

2021 ◽  
pp. 11-12
Author(s):  
Deepika Jain ◽  
Shilpa Rathor

The present paper describes the kinetics of oxidation of l-Arginine by QDC in the presence of perchloric acid in 30% DMF-H O(v/v) medium at 2 + 40⁰C spectrophotometrically at λ =354nm. The reaction is rst order with respect to [QDC], [H ], and [substrate]. The reaction rate increased with max increasing volume percentage of DMF in reaction mixture. Michaelis- Menten type kinetic was observed with l-Arginine. The reaction rates were studied at different temperature and the activation parameters has been computed. The main product was identied as Cr (III) and 4-Guanidino buteraldehyde.


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