Quinolinium dichromate (QDC) in sulfuric acid oxidizes benzaldehydes to the corresponding acids in a 50% (v/v) acetic acid-water medium. The reaction is first order each in [QDC], [substrate] and [H+]. The reaction rates have been determined at different temperatures and the activation parameters calculated. The rate decreases with an increase in the water content of the medium. The effects of substituents have been studied. A suitable mechanism is proposed.
Received: 2003-6-23
Published Online: 2014-6-2
Published in Print: 2003-12-1
© 1946 – 2014: Verlag der Zeitschrift für Naturforschung
You are currently not able to access this content.
You are currently not able to access this content.
Articles in the same Issue
- Atomvolumen, Packungsdichte undWertigkeit von Caesium unter Druck Atomic Volume, Packing Density and Valence of Cesium under Pressure
- Dinuclear Nickel(II) and Palladium(II) Complexes in Combination with Different Co-Catalysts as Highly Active Catalysts for the Vinyl/Addition Polymerization of Norbornene
- Synthesis and Characterization of N-Methyl-Substituted Germocanes. Crystal Structure of MeN(CH2CH2O)2GeBr2
- Molecular Structure and Thermal Analysis of Potassium Hydrogenphthalate Monohydrate
- Synthese flexibler difluorierter cyclopropanoider Nucleosidanaloga / Synthesis of Flexible Difluorinated Cyclopropanoid Nucleoside Analogues
- Electroreduction of Organic Compounds, 34 [1]. Cathodic Dehalogenation of Chloroarenes with Electron-Donating Substituents
- Kinetics of Oxidation of Benzaldehydes by Quinolinium Dichromate
- New Isoflavonoid from Dipterix odorata
- Frankiamide: A Structural Revision to Demethyl (C-11) Cezomycin
- Xyloccensin M and N, Two New B, D-seco Limonoids from Xylocarpus granatum
- Titanyl Acetylacetonate as an Efficient Catalyst for a Mild and Convenient Reduction of Carbonyl Compounds with NaBH4 under Aprotic Condition
- A Convenient Synthesis of New Pentaazacyclopentanaphthalene and Pentaazaphenanthrene Derivates
- A New Pyranoacridone Alkaloid from the Bark of Medicosma subsessilis (Rutaceae)
- Synthesis of Some New Furocoumarins and their Usage in Peptide Synthesis
- Isolation, Structure Elucidation and Activity of Anthracycline Acetates from a Terrestrial Streptomyces sp.
- Synthesis of Spacered Cyclopropanoid Muramyldipeptide Analogues as Potential Immunostimulants
Keywords for this article
Kinetic;
Oxidation;
Aromatic Aldehydes;
Quinolinium Dichromate
Articles in the same Issue
- Atomvolumen, Packungsdichte undWertigkeit von Caesium unter Druck Atomic Volume, Packing Density and Valence of Cesium under Pressure
- Dinuclear Nickel(II) and Palladium(II) Complexes in Combination with Different Co-Catalysts as Highly Active Catalysts for the Vinyl/Addition Polymerization of Norbornene
- Synthesis and Characterization of N-Methyl-Substituted Germocanes. Crystal Structure of MeN(CH2CH2O)2GeBr2
- Molecular Structure and Thermal Analysis of Potassium Hydrogenphthalate Monohydrate
- Synthese flexibler difluorierter cyclopropanoider Nucleosidanaloga / Synthesis of Flexible Difluorinated Cyclopropanoid Nucleoside Analogues
- Electroreduction of Organic Compounds, 34 [1]. Cathodic Dehalogenation of Chloroarenes with Electron-Donating Substituents
- Kinetics of Oxidation of Benzaldehydes by Quinolinium Dichromate
- New Isoflavonoid from Dipterix odorata
- Frankiamide: A Structural Revision to Demethyl (C-11) Cezomycin
- Xyloccensin M and N, Two New B, D-seco Limonoids from Xylocarpus granatum
- Titanyl Acetylacetonate as an Efficient Catalyst for a Mild and Convenient Reduction of Carbonyl Compounds with NaBH4 under Aprotic Condition
- A Convenient Synthesis of New Pentaazacyclopentanaphthalene and Pentaazaphenanthrene Derivates
- A New Pyranoacridone Alkaloid from the Bark of Medicosma subsessilis (Rutaceae)
- Synthesis of Some New Furocoumarins and their Usage in Peptide Synthesis
- Isolation, Structure Elucidation and Activity of Anthracycline Acetates from a Terrestrial Streptomyces sp.
- Synthesis of Spacered Cyclopropanoid Muramyldipeptide Analogues as Potential Immunostimulants