because apparently, propanone is a ketone, and ketons do not have a hydrogen which could get oxidised, unlike aldehydes which do.
ethanal
ethanal and propanone both are carbonyl compounds but ethanal shows reducing properties due to presence of hydrogen on carbonyl group it reduces tollens fehling solution schiffs reagent
Ethanol burns readily in a plentiful supply of air to form carbon dioxide and water. In a very limited amount of air carbon or carbon monoxide may be formed. In the test tube it is oxidised to ethanal and then ethanoic acid by such reagents as acidified potassium dichromate solution. Oxidation to ethanoic acid by oxygen is catalysed by the enzymes in certain bacteria (acetobacter).
Ethanol (CH3CH2OHl) + KMnO4 ----> Ethanal (CH3CHO) -----> Ethanoic Acid (CH3COOH) Primary Alcohol Oxidized ---> Aldehyde Oxidized---> Carboxyilic Acid You could attain Ethanal by using the oxidizing agent Pyridinium Chlorochromate (PCC) anhydrously.
There are four hydrogen atoms in an ethanal molecule, CH3CHO.
Some other names for ethanal include acetaldehyde, acetic aldehyde, and ethyl aldehyde. Ethanal is actually the IUPAC name for the organic chemical compound acetaldehyde.
Yes.
The chemical formula of ethanal (acetic aldehyde) is CH3CHO.
Ethanal = C2H4O O.S of O = -2 O.S. of H = +1 O.S. of C = -1
ethanal font:wikipedia
Aldehydes
yes