The kinetics of reaction between aliphatic ℓ-amino acids and 1,3-dichloro-5,5-dimethylhydantoin have been studied in aqueous acetic acid medium yielding aliphatic aldehydes as the end-products by the ring cleavage oxidation. The catalytic effect of acid in the reaction rate reveal an interaction between oxidants species H2O+Cl and substrates. The observed order of reactivity ℓ-amino acids (ℓ-Glycine > ℓ-Alanine) was explained on the basis of conformational considerations. A plausible mechanism and rate law supported by thermodynamic parameters was discussed.
aliphatic aldehydes, demonstrates, reveals, plausible.
IRE Journals:
Dr. Arvind Prasad Dwivedi , Shweta Neeraj
"Oxidative And Thermodynamic Study Of Aliphatic Amino Acids By 1,3-dichloro-5,5-dimethylhydantoin In Aqueous Acetic Acid Medium " Iconic Research And Engineering Journals Volume 2 Issue 5 2018 Page 38-41
IEEE:
Dr. Arvind Prasad Dwivedi , Shweta Neeraj
"Oxidative And Thermodynamic Study Of Aliphatic Amino Acids By 1,3-dichloro-5,5-dimethylhydantoin In Aqueous Acetic Acid Medium " Iconic Research And Engineering Journals, 2(5)