Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/43806
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dc.contributor.authorSrinivasan, Vangalur S-
dc.contributor.authorRamakrishnan, Kalyani-
dc.date.accessioned2018-03-13T06:59:06Z-
dc.date.available2018-03-13T06:59:06Z-
dc.date.issued1993-04-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/43806-
dc.description338-340en_US
dc.description.abstractThe kinetics of regeneration of carbonyl compounds from anil of benzaldehyde and benzophenone by MnIII(OAc)3 have been studied at 29 ± 0.1ᵒC in aq. acetic acid (76%, v/v). The corresponding aldehyde/ketone is formed in about 96% yield along with nearly 48% of azobenzene in about 3-4 hr. One mol of anil consumes nearly 2 mol of MnIII(OAc)3 for the reaction. The reaction is less susceptible to the electronic influence of substituents

on both benzaldehyde and aniline portions. A mechanism involving addition of MnIII(OAc)3 to C = N in the rate determining step has been envisaged to account for the results.

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.32A(04) [April 1993]en_US
dc.titleFacile regeneration of carbonyl compounds from anils by manganese(III) triacetate- A kinetic studyen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.32A(04) [April 1993]

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