Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/39964
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSenapati, S-
dc.contributor.authorDash, P K-
dc.contributor.authorMishra, B K-
dc.contributor.authorBehera, G B-
dc.date.accessioned2017-02-01T05:08:26Z-
dc.date.available2017-02-01T05:08:26Z-
dc.date.issued1995-03-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/39964-
dc.description227-229en_US
dc.description.abstractThe schiff bases .of the type (p-C 16H33O-C6H4CH=N)2(CH2)m (1, m=O, 2, 3, 4 and 6) and the ortho isomer (2, m = 0, 2, 4, 6) have been synthesized and the hydrolysis of these compounds have been studied in CTAB-CHCl3,-H2O reversed micellar system under acidic condition. Significant variation of the reaction rate has been observed due to variation in the number of methylene groups in the spacer and due to the change in the position of the cetyloxy group. Difference in the rate of disappearance of schiff base and appearance of the product is ascribed to a mechanism involving a carbinolamine intermediate.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.34A(03) [March 1995]en_US
dc.titleHydrolysis of schiff bases in (CTAB-CHCl3-H2O) reversed micelles: Role of spacersen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.34A(03) [March 1995]

Files in This Item:
File Description SizeFormat 
IJCA 34A(3) 227-229.pdf737.77 kBAdobe PDFView/Open


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