Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/39954
Title: Reactivity of Schiff base : Part-3 -Amination of 2-/4-hydroxybenzylidene-2- aminobenzothiozole
Authors: Mishra, R K
Hota, (Mrs) S
Mishra, B K
Behera, G B
Issue Date: Mar-1998
Publisher: NISCAIR-CSIR, India
Abstract: The amination reactions of 2-/4-hydroxybenzylidene-2-aminobenzothiazole (1a and 1b respectively) have been kinetically studied in chloroform medium. 1a is found to react faster than 1b. Both kinetic and spectral data support aggregation of both la and lb in the experimental conditions. Aniline is also found to aggregate in chloroform beyond a limiting concentration. The higher reactivity of la supports the entrapment mechanism in which aniline molecule is entrapped by 1a making it more reactive than 1b. The reactivity of aniline is explained both by intra and inter molecular catalysis. The curvature in the plot of rate constant versus [substrate] has been explained by proposing an aggregation of the substrates in chloroform.
Page(s): 200-205
URI: http://nopr.niscair.res.in/handle/123456789/39954
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.37A(03) [March 1998]

Files in This Item:
File Description SizeFormat 
IJCA 37A(3) 200-205.pdf517.35 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.