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no, because it does not react with aromatic aldehydes
Does not react. Because Tollens' reagent only works with aldehydes. Butanone is methyl ethyl ketone (MEK).
aldehydes have at least one hydrogen bond in their structure,hence they do not cause much hindrances to attacking nucleophiles.ketones on the other hand have at least 2 methyl groups attached to their structure hence,the methyl group cause steric strains hence makes it difficult for the attacking nucleophile to bond with the carbonyl carbon.in this case aldehydes wiil be able to react with nuclephiles faster than ketones.
No because it doesn't contain aromatic group
None. helium doesnt react with any other element
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.
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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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.
The Benedict reagent is not for sodium chloride testing.
Because chromic acid is an oxidizing agent.
Ketones or Aldehydes DO NOT react with Sodium Bicarbonate..generally only Carboxilic acids have the ability to do it!
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.
An alkane will react with the bromine test and become a clear/colourless liquid, while an aromatic hydrocarbon will not react with the bromine and remain a redish-orange tinged liquid.
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.
It doesnt