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dc.contributor.authorShrivastava, Ruchi-
dc.contributor.authorMishra, Sangeeta-
dc.contributor.authorSengupta, Susanta K-
dc.date.accessioned2008-04-30T10:16:38Z-
dc.date.available2008-04-30T10:16:38Z-
dc.date.issued2007-06-
dc.identifier.issn0376-4710-
dc.identifier.urihttp://hdl.handle.net/123456789/1207-
dc.description933-936en_US
dc.description.abstractA chemometric analysis of equilibrium results for apolar aprotic solvent effects on proton transfer between m-/o-chlorobenzoic acids and crystal violet carbinol base using Koppel-Palm’s approach shows that the total solvent effect is contributed mainly by dispersion and dipolar/electrostatic interactions in approximately 7:4 ratio. A parallel study with m- and o-fluorobenzoic acids but under conditions favouring acid-acid anion homoconjugation reflects the role of homoconjugated complexed acids in substantially modifying the detailed pattern of solvent effects.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCA Vol.46A(6) [June 2007]en_US
dc.titleInfluence of apolar aprotic solvents on proton transfer equilibrium between m-/o-chlorobenzoic acids and the carbinol base of crystal violet: A chemometric analysisen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.46A(06) [June 2007]

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