Examples of using Aldehyde in English and their translations into Spanish
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If the carbonyl group is an aldehyde, the monosaccharide is an aldose;
The cumin aldehyde present in the volatile oil is readily converted artificially into thymol.
When the dithiane is derived from an aldehyde such as acetaldehyde the acyl proton can be abstracted by n-butyllithium in THF at low temperatures.
The Angeli-Rimini reaction is an organic reaction between an aldehyde and the sulfonamide N-hydroxybenzenesulfonamide in presence of base forming a hydroxamic acid.
It is the simplest aromatic aldehyde and one of the most industrially useful.
The Bodroux-Chichibabin aldehyde synthesis is a chemical reaction whereby a Grignard reagent is converted to an aldehyde one carbon longer.
The special catalyst is needed to avoid further reduction of the aldehyde group to a hydroxyl group,
of a sugar with the aldehyde at carbon 1.
which may react enantioselectively with suitable aldehyde electrophiles.
the thermodynamic product is a ketone or aldehyde.
the C-C bond in a vicinal diol is cleaved with formation of ketone or aldehyde functional groups.
The Fischer oxazole synthesis is a chemical synthesis of an oxazole from a cyanohydrin and an aldehyde in the presence of anhydrous hydrochloric acid.
The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a(substituted) phenylhydrazine and an aldehyde or ketone under acidic conditions.
Dinitrophenylhydrazine can be used to qualitatively detect the carbonyl functionality of a ketone or aldehyde functional group.
Most notably periodic acid will cleave vicinal diols into two aldehyde or ketone fragments.
Aldehyde and phenol-free concentrate disinfectant for clinical instruments,
Human skin also contains aldehyde functional groups in the termini of saccharides
The first step of the Bouveault aldehyde synthesis is the formation of the Grignard reagent.
Bouveault aldehyde synthesis G. Bryant Bachman(1943)."n-Hexaldehyde.
The Cannizzaro reaction is a competing reaction when two aldehyde molecules react by disproportionation to form the corresponding alcohol and carboxylic acid.