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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Char, P Narasimha | - |
| dc.contributor.author | Sondu, S | - |
| dc.contributor.author | Sethuram, B | - |
| dc.contributor.author | Rao, T Navaneeth | - |
| dc.date.accessioned | 2019-03-26T03:51:19Z | - |
| dc.date.available | 2019-03-26T03:51:19Z | - |
| dc.date.issued | 1989-01 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/46604 | - |
| dc.description | 36-39 | en_US |
| dc.description.abstract | Kinetics of Ru(III) chloride catalysed oxidation of chalcone and some substituted chalcones by acid bromate have been studied in acetic acid-sulphuric acid medium in the temperature range 303-318 K. The reaction is first order each in [chalcone] and [Ru(III)] and zero order each in [H +] and [BrO )]. The rate increases with increase in the percentage of acetic acid and the plot of log ko versus 1/D is linear with a positive slope indicating the positive ion-dipole nature of the reaction. The order of reactivities of various substituted chalcones with substituents in phenyl ring is: p-CH3 > m-CH3 > H > p-Cl > m-NO2 > p-NO2. A radical mechanism involving the chalcone and Ru(III) in the slow step followed by oxidation of Ru(II) by BrO to Ru(III) in the fast step is proposed. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.28A(01) [January 1989] | en_US |
| dc.title | Kinetics of Ru (III)-catalysed Oxidation of Chalcones by Acid Bromate in H2SO4 -HOAc Medium | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.28A(01) [January 1989] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 28A(1) 36-39.pdf | 2.13 MB | Adobe PDF | View/Open |
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)]. The rate increases with increase in the percentage of acetic acid and the plot of log ko versus 1/D is linear with a positive slope indicating the positive ion-dipole nature of the reaction. The order of reactivities of various substituted chalcones with substituents in phenyl ring is: p-CH3 > m-CH3 > H > p-Cl > m-NO2 > p-NO2. A radical mechanism involving the chalcone and Ru(III) in the slow step followed by oxidation of Ru(II) by BrO