• Radhika Rathi
• Arpita Vyas
• Anjali Purohit
• Shweta Vyas
• Pradeep K. Sharma

Kinetics and mechanism of oxidation of formic and oxalic acids by pyridinium dichromate (PDC) have been studied in dimethylsulphoxide. The main product of oxidation is carbon dioxide. The reaction is first order with respect to PDC. Michaelis Menten type of kinetics were observed with respect to the reductants. The reaction is acid catalysed and the acid dependence has the form: kobs = a + b[H+]. The oxidation of  deuterio formic acid exhibits a substantial primary kinetic isotope effect (kH/kD = 5.77 at 298 K). The reaction has been studied in nineteen different organic solvents and the solvent effect has been analysed using Taft's and Swain's multiparametric equations. The temperature dependence of the kinetic isotope effect indicates the presence of a symmetrical cyclic transition state in the rate determining step. Suitable mechanisms have been proposed.

Acids, Dichromate, Kinetics, Mechanism, Oxidation

"Oxidation Kinetics and Mechanistic Studies of Organic Acids by Pyridinium Dichromate", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.6, Issue 5, page no.386-392, May-2019, Available :http://www.jetir.org/papers/JETIR1905558.pdf

"Oxidation Kinetics and Mechanistic Studies of Organic Acids by Pyridinium Dichromate", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.6, Issue 5, page no. pp386-392, May-2019, Available at : http://www.jetir.org/papers/JETIR1905558.pdf