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Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.
The first one consists on thermally converting calcium carboxylate salts into the corresponding ketones. This was a common method for making acetone from calcium acetate during World War I. [6] The other method for making ketones consists on converting the vaporized carboxylic acids on a catalytic bed of zirconium oxide. [7]
To convert from / to /, divide by 10. To convert from / to ... Water: 5.536 0.03049 Xenon: 4.250 0.05105 Units. 1 J·m 3 /mol 2 = 1 m 6 ·Pa/mol 2 = 10 L 2 ·bar/mol 2.
In organic chemistry, carbonyl reduction is the conversion of any carbonyl group, usually to an alcohol. It is a common transformation that is practiced in many ways. [ 1 ] Ketones , aldehydes , carboxylic acids , esters , amides , and acid halides - some of the most pervasive functional groups , -comprise carbonyl compounds.
Scientific evidence reveals that water is an inhibitor for corrosion by ethanol. [6] The experiments are done with E50, which is more aggressive and speeds up the corrosion effect. It is very clear that by increasing the amount of water in fuel ethanol one can reduce corrosion. At 2% or 20,000 ppm water in the ethanol fuel the corrosion stopped.
An α,β-epoxyketone reacts with hydrazine hydrate to yield an allylic alcohol. [7] In the synthesis of warburganal, a bioactive natural product, the α,β-epoxyketone is formed from a cyclic α,β-unsaturated ketone and in a separate step reacts under the classical Wharton olefin synthesis conditions to yield an allylic diol. [8]
Enantioselective ketone reductions convert prochiral ketones into chiral, non-racemic alcohols and are used heavily for the synthesis of stereodefined alcohols. [ 1 ] Carbonyl reduction, the net addition of H 2 across a carbon-oxygen double bond, is an important way to prepare alcohols.
Water and carbon dioxide are byproducts: [1] 2 RCO 2 H → R 2 CO + CO 2 + H 2 O. Bases promote this reaction. The reaction mechanism is proposed to involve nucleophilic attack of the alpha-carbon of one acid group on the other carboxylic acid group, possibly as a concerted reaction with the decarboxylation. [1]