Mechanistic aspects of oxidation of dextrose by N-bromophthalimide in acidic medium: a micellar kinetic study

2012 ◽  
Vol 39 (2) ◽  
pp. 469-484 ◽  
Author(s):  
Minu Singh
Keyword(s):  
2015 ◽  
Vol 41 (1) ◽  
pp. 77-85 ◽  
Author(s):  
Thangamariyappan Shanmugaprabha ◽  
Karuppaiah Selvakumar ◽  
Kasi Rajasekaran ◽  
Ponnusamy Sami

2010 ◽  
Vol 35 (4) ◽  
pp. 407-414 ◽  
Author(s):  
Ajaya Kumar Singh ◽  
Bhawana Jain ◽  
Reena Negi ◽  
Yokraj Katre ◽  
Surya P. Singh ◽  
...  

The Analyst ◽  
1972 ◽  
Vol 97 (1155) ◽  
pp. 412 ◽  
Author(s):  
D. J. B. Galliford ◽  
J. M. Ottaway

2015 ◽  
Vol 41 (1) ◽  
pp. 25-34
Author(s):  
Ali A. G. A. Al Mahdi ◽  
Mohammed A. Hussein ◽  
Eleanor Fourie ◽  
Jannie C. Swarts ◽  
C. Robert Dennis

2021 ◽  
Vol 11 ◽  
Author(s):  
Nitin Sharma ◽  
Tanveer Alam ◽  
Ashok Kumar

Aims: This study aims at the Kinetic Study of Iodination of Propanone in Different Acidic Medium by using Colorimeter. Background: The kinetic experimentation of iodination of propanone has been performed in presence of different acids such as sulphuric acid, hydrochloric acid and acetic acid. The rate law of the iodination of propanone in acidic medium is determined by observing the disappearance of the brownish yellow colour of iodine in aqueous solution. Objective: The objective of this study is the preparation of standard solution, determination of absorbance of iodine solution at λmax= 480 nm, Kinetic study of iodination of propanone with different acidic medium. Method: The kinetic analysis of this reaction has been carried out by colorimetry. The extent of the reaction has been monitored by measuring the absorbance of the reaction mixture after a suitable time interval. Result: The rate law expression is determined to be rate = k [〖"propanone]" 〗_0^0.728 [acid]0. The rates of iodination of propanone in presence of different acidic medium are H2SO4 > HCl > CH3COOH. Conclusion: The rate of the reaction is found to be independent of the concentration of iodine i.e. it is zero order reaction with respect to iodine. However, it depends on the concentration of propanone and acid catalyst. Other: By using this experimental technique, the consumption of chemicals is very less.


Polyhedron ◽  
2014 ◽  
Vol 81 ◽  
pp. 409-413 ◽  
Author(s):  
Ali A.G.A. Al Mahdi ◽  
Mohammed A. Hussein ◽  
Chris C. Joubert ◽  
Jannie C. Swarts ◽  
C. Robert Dennis
Keyword(s):  

1976 ◽  
Vol 29 (7) ◽  
pp. 1449 ◽  
Author(s):  
V Balasubramanian ◽  
V Thiagarajan

The chlorination of acetone in aqueous acidic medium in the presence of acetic acid and dimethylformamide was subjected to kinetic study. Although the kinetics follows the traditional mechanism at high concentrations of chloramine-T (cat) and in aqueous acetic acid in the presence of sodium acetate, a term in the rate law independent of ketone concentration is reported for the first time in strongly acidic medium at low concentrations of chloramine-T. Generation of the chlorinating species is considered as the rate-determining step (Scheme 1). The mechanistic changes which occur on addition of chloride and on changing the structure of the ketone are reported. The effect of acetate on the rate in aqueous acetic acid medium is rationalized by invoking a prior equilibrium formation of enolate followed by a rate-controlling chlorination by chlorinium acetate. The retardation in rate and the consequent changes in mechanism in the case of p-bromo- and p-nitroacetophenone are accounted for by invoking a complex between the enol and the positive chlorine species similar to that in the mechanism for the chlorination of phenols.


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