no, because it does not react with aromatic aldehydes
Typically aromatic groups attached to functional groups increase the reaction over that of an aliphatic groups. Aromatic aldehydes (e.g. benzaldehyde, C6H5.CHO), are also known which undergo a number of chemical reaction which do nor occur for aliphatic aldehydes and which are unique to aromatic aldehydes.
No, the Tollen's Silver Mirror Test only confirms the presence of aldehydes.
KCN does not react with aldehydes and ketones because these compounds do not have an acidic hydrogen that can be removed to form an enolate ion, which is necessary for nucleophilic addition reactions with cyanide ions. Aldehydes and ketones lack the necessary alpha carbon acidity to undergo this reaction with KCN.
Yes, cinnamaldehyde can react with Fehling's reagent to form an orange-red precipitate of copper(I) oxide. This is because aldehydes are capable of reducing the copper(II) ions present in the Fehling's reagent to form the insoluble copper(I) oxide.
no, because it does not react with aromatic aldehydes
The properties of aromatic aldehydes like benzaldehyde is that they are colorless liquids that are slightly soluble in water. They smell of almonds and react similar to their aliphatic analogues.
Typically aromatic groups attached to functional groups increase the reaction over that of an aliphatic groups. Aromatic aldehydes (e.g. benzaldehyde, C6H5.CHO), are also known which undergo a number of chemical reaction which do nor occur for aliphatic aldehydes and which are unique to aromatic aldehydes.
The properties of aromatic aldehydes like benzaldehyde is that they are colorless liquids that are slightly soluble in water. They smell of almonds and react similar to their aliphatic analogues.
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The Benedict reagent is not for sodium chloride testing.
Ketones or Aldehydes DO NOT react with Sodium Bicarbonate..generally only Carboxilic acids have the ability to do it!
No, the Tollen's Silver Mirror Test only confirms the presence of aldehydes.
In the bromine test, an alkene compound will decolorize a bromine solution whereas an aromatic compound will not react with the bromine solution. This is because the double bond in the alkene readily reacts with bromine to form a colorless product, while the stable aromatic ring in the aromatic compound does not undergo such reaction.
KCN does not react with aldehydes and ketones because these compounds do not have an acidic hydrogen that can be removed to form an enolate ion, which is necessary for nucleophilic addition reactions with cyanide ions. Aldehydes and ketones lack the necessary alpha carbon acidity to undergo this reaction with KCN.
Benedicts reagent tests for reducing sugars, so the question is, is raffinose a reducing sugar. Raffinose is a trisaccharide made up of glucose, fructose and galactose. It is not a reducing sugar because all of its anomeric carbons are bonded, so it will not react with benedicts reagent.
Quasi aromatic compounds are ionic in nature, there is a presence of counter ion e.g. when tropone react with HClO4 quasi aromatic compound is formed.