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dc.contributor.authorLowe, Barrie M.-
dc.contributor.authorSmith, David G.-
dc.date.accessioned2025-06-24T09:37:12Z-
dc.date.available2025-06-24T09:37:12Z-
dc.date.issued1974-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18980-
dc.description.abstractThe primary acidity constant of maleic acid has been determined at 298.2 K in ordinary water by conductance measurements and in both ordinary water and deuterium oxide by precise e.m.f. measure ments with glass and silver-silver chloride electrodes in a cell without liquid junctions. Both methods give pKh values which increase with the applied ion-size parameter a and which are identical (pKii = 2.038 + 0.008) when 1010 a/m = 5 is used. The isotope effect ApK = pKn —pKn decreases slightly with a but for all reasonable ion-size parameters it has an abnormally high value (e.g. ApK = 0.561 ± 0.012 when IO10 a/m = 5) which may be due to internal hydrogen bonding in its anion. For 3 < 1010 a/m<7 the pKn-values are significantly higher than that generally accepted, and the ApK values support the lower of the two previous ones.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1974, 70 (1-6)en_US
dc.subjectChemistryen_US
dc.subjectAcidity Constanten_US
dc.subjectMaleic Aciden_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titlePrimary Acidity Constant of Maleic Acid in Ordinary Water and in Deuterium Oxideen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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