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dc.contributor.authorSondu, S-
dc.contributor.authorSethuram, B-
dc.contributor.authorRao, T Navaneeth-
dc.date.accessioned2019-03-20T07:05:16Z-
dc.date.available2019-03-20T07:05:16Z-
dc.date.issued1990-01-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46253-
dc.description67-69en_US
dc.description.abstractThe base-catalysed condensation of benzaldehydes with acetophenones is enhanced by electron-withdrawing substituents in both the starting compounds. The magnitude of ρ-value obtained for various substituents in the benzaldehyde moiety decreases with the introduction of electron-withdrawing groups in the para position of acetophenone moiety.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.29A(01) [January 1990]en_US
dc.titleInteractive free energy relationships for non-additive multiple substituent effects in base catalysed condensation of benzaldehydes with acetophenones: A kinetic studyen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.29A(01) [January 1990]

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