Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/15713
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dc.contributor.authorRamesh, B-
dc.contributor.authorSadanand, D Thomas-
dc.contributor.authorSwamy, K Venkata-
dc.contributor.authorSaiprakash, P K-
dc.date.accessioned2013-01-10T18:38:36Z-
dc.date.available2013-01-10T18:38:36Z-
dc.date.issued1999-05-
dc.identifier.urihttp://hdl.handle.net/123456789/15713-
dc.description462-467en_US
dc.description.abstractHydrogenation of some allylic alcohols like 2-methyl-2-propen- l-ol, 4-penten-3-ol, trans-2-buten-l -ol, trans-3-penten-2-ol and 4- methyl-3-penten-2-ol has been carried out by anchored  montmorillonitebipyridinepalladium(II) acetate in THF medium. Under the reaction conditions 100% saturation of carbon-carbon double bond is observed and there is neither polymerisation nor isomerisation. The observed rate has been found to be first order each with respect to partial pressure of hydrogen and [substrate] and fractional order with respect to [catalyst] . The rate of hydrogenation follows the order: 2-methyl-2-propen-l-ol > 4-penten-3-ol > trans-2-buten-l-ol > trans -3-penten-2-ol > 4-methyl-3-penten-2-ol. Thermodynamic parameters have been evaluated, rate law and a plausible mechanism have been proposed.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.38A(05) [May 1999]en_US
dc.titleHydrogenation of some allylic alcohols catalysed by anchored montmorillonitebipyridinepalladium(II) acetate - A kinetic studyen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.38A(05) [May 1999]

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