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Fétizon oxidation is the oxidation of primary and secondary alcohols utilizing the compound silver(I) carbonate absorbed onto the surface of celite also known as Fétizon's reagent first employed by Marcel Fétizon in 1968. [1]
In organic chemistry, a carbonate ester (organic carbonate or organocarbonate) is an ester of carbonic acid. This functional group consists of a carbonyl group flanked by two alkoxy groups. The general structure of these carbonates is R−O−C(=O)−O−R' and they are related to esters ( R−O−C(=O)−R' ), ethers ( R−O−R' ) and also to ...
Sodium carbonate is obtained as three hydrates and as the anhydrous salt: sodium carbonate decahydrate , Na 2 CO 3 ·10H 2 O, which readily effloresces to form the monohydrate. sodium carbonate heptahydrate (not known in mineral form), Na 2 CO 3 ·7H 2 O. sodium carbonate monohydrate (thermonatrite), Na 2 CO 3 ·H 2 O. Also known as crystal ...
One workaround to avoid this method is to reduce the carboxylic acid derivative all the way down to an alcohol, then oxidize the alcohol back to an aldehyde. Other alternatives include forming a thioester or a Weinreb amide, then reducing the new species to an aldehyde through the Fukuyama reduction or Weinreb reaction respectively, or using ...
There are other reactions of carbonyl compounds similar to aldol condensation: When the base is an amine and the active hydrogen compound is sufficiently activated the reaction is called a Knoevenagel condensation. In a Perkin reaction the aldehyde is aromatic and the enolate generated from an anhydride.
Bucherer improved on Bergs’ method, finding that lower temperatures and pressures for the reaction were permissible. Bucherer and Steiner also found that cyanohydrins would react just as well as carbonyl compounds to produce hydantoins. Later, Bucherer and Lieb found that 50% alcohol was an effective solvent for the reaction.
The College Football Playoff selection committee enters its final two weeks of deliberation with a host of consequential decisions thrust on the 13 members.
Under ideal conditions the reaction produces 50% of both the alcohol and the carboxylic acid (it takes two aldehydes to produce one acid and one alcohol). [5] This can be economically viable if the products can be separated and both have a value; the commercial conversion of furfural into furfuryl alcohol and 2-furoic acid is an example of this ...