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Does water react to the Benedict test?

no, because it does not react with aromatic aldehydes


What are the Properties of aromatic aldehyde?

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.


How will you characterize the rate of reaction of an aldehyde compared to an aliphatic aldehyde?

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.


What are the properties of aldehyde?

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.


How does benedicts solution react with orange juice?

cock


How does sodium chloride react with Benedicts?

The Benedict reagent is not for sodium chloride testing.


How does ketones react with sodium bicarbonate?

Ketones or Aldehydes DO NOT react with Sodium Bicarbonate..generally only Carboxilic acids have the ability to do it!


Does the tollens test deal with alkenes?

No, the Tollen's Silver Mirror Test only confirms the presence of aldehydes.


When preforming the bromine test to distinguish between aromatic and alkene compound?

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.


Why KCN fail to react with aldehyde and ketones?

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.


Would raffinose react with benedicts reagent?

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.


What is quasi aromaticity?

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.