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Acids, Carboxylates, and Carbonyl Compounds

The oxidation of methylmalonic and ethylmalonic acids (LH2) by Ce(IV) in acidic aqueous solution/ equation (90), [Pg.86]

Oxalate complexes of Mn(III) decompose to Mn(II) and CO2. The rate-determining step is a unimolecular formation of Mn(II) and COJ. The radical scavenger acrylic acid has little effect on the rate, indicating that [Pg.86]

Cr(IV), produced in situ from Cr(VI) and V(IV), oxidizes Co(III) complexes of mandelic, lactic, and benzilic acids with the rate law in equation (92)  [Pg.87]

A deuterium kinetic isotope effect of 6.1 was observed in the oxidation of acetaldehyde by permanganate in aqueous HC104, implying a hydride [Pg.87]

Aliphatic esters are oxidized by chromic acid in acetic acid-HzO mixtures. The reaction shows an unusually strong dependence An increase in [H2SO4] from 2 to 3.5 M causes a 38-fold increase in rate. The rate acceleration by oxalic acid was explained by a three-electron mechanism. [Pg.88]


See other pages where Acids, Carboxylates, and Carbonyl Compounds is mentioned: [Pg.86]    [Pg.87]   


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Acidic carbonyl

Carbonyl carboxylate

Carbonyl compounds carboxylic acids and derivatives

Carboxyl compound

Carboxylation compounds

Carboxylic acid Carbonyl compounds

Carboxylic acids compounds

Carboxylic acids, acidity compounds

Chiral Isocyanides, Carboxylic Acids and Carbonyl Compounds

Compounds acids and

Unit 7.2 Carbonyl Compounds and Carboxylic Acids

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