Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/1151
Title: Kinetics and mechanism of the hydroxylation of some naphthalene sulphonic acid derivatives by peroxodisulphate
Authors: Abdel-Khalek, Ahmed A
Hassan, Eman S
Hassan, Hala M
Keywords: Oxidation
Oxidation
Peroxodisulphate
Kinetics
Chromotropic acid
1-Amino-4-naphthalene sulphonic acid
Issue Date: Sep-2007
Publisher: CSIR
Series/Report no.: C07C7/00
Abstract: Oxidation of 1,8-dihydroxynaphthalene-3,6-disulphonic acid (CTA) and 1-amino-4-naphthalene sulphonic acid (ANS) by potassium peroxodisulphate leads to hydroxylation of these organic compounds. These oxidations may proceed through inner-sphere electron transfer as in case of ANS or by outer-sphere mechanism in case of CTA. The homolytic fission of S₂O₈²⁻ is the rate determining step in the oxidation of CTA by S₂O₈²⁻, whereas, the intramolecular electron transfer in the precursor compounds is the rate determining step in the mechanism of oxidation of ANS. Hydroxylation takes place in para-position of benzene ring in CTA and ortho-position in ANS. The thermodynamics activation parameters were calculated. Rate of oxidation of both CTA and ANS in methanol-water solvent mixtures is decreased by increasing methanol content in the medium.
Description: 466-472
URI: http://hdl.handle.net/123456789/1151
ISSN: 0971–457X
Appears in Collections:IJCT Vol.14(5) [September 2007]

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