tollen reagent
2[Ag(NH3)2]OH is tollen's reagent
Tollens' reagent is used to determine whether a carbonyl containing compound is an aldehyde or a ketone. Acetone is a ketone so it will not readily react with Tollens' reagent.
because
ch61206
yes!!
Pyrrole-2-aldehyde does not respond to Tollens reagent because it is not a reducing sugar. Tollens reagent (silver nitrate) is used to test for the presence of aldehyde groups, which are commonly found in reducing sugars. Reducing sugars contain aldehyde groups and are capable of donating electrons to Tollens reagent, forming a silver mirror on the test tube wall. Pyrrole-2-aldehyde does not contain aldehyde groups, and therefore is not a reducing sugar. As a result, it does not react with Tollens reagent.
Tollens' reagent is used to determine whether a carbonyl containing compound is an aldehyde or a ketone. Acetone is a ketone so it will not readily react with Tollens' reagent.
ch61206
because
yes!!
Does not react. Because Tollens' reagent only works with aldehydes. Butanone is methyl ethyl ketone (MEK).
Pyrrole-2-aldehyde does not respond to Tollens reagent because it is not a reducing sugar. Tollens reagent (silver nitrate) is used to test for the presence of aldehyde groups, which are commonly found in reducing sugars. Reducing sugars contain aldehyde groups and are capable of donating electrons to Tollens reagent, forming a silver mirror on the test tube wall. Pyrrole-2-aldehyde does not contain aldehyde groups, and therefore is not a reducing sugar. As a result, it does not react with Tollens reagent.
2[Ag(NH3)2]OH is tollen's reagent
The outcome of the Tollens reagent reacting with methanal (formaldehyde), ethanol (ethyl alcohol), and propanone (acetone) is the formation of metallic silver (Ag) in the case of methanal, while ethanol and propanone do not show a significant reaction with Tollens reagent. Tollens reagent is used as a chemical test to distinguish between aldehydes and ketones, where aldehydes react to produce a silver mirror, while ketones do not react.
no negative
vanillin violently reacts with Bromine in carbon tetrachloride,tollens reagent and aqueous NaOH
No.While vanillin is an aldehyde, which should react with Tollens' reagent to precipitate silver metal, vanillin does not "pass" Tollens' test. Tollens' reagent is very basic (sodium or potassium hydroxide). Vanillin has a phenolic hydrogen (OH bonded to a phenyl ring) which is slightly acidic. Vanillin will react first with the excess hydroxide ions in solution to form a phenoxide salt, which will not participate in the silver-precipitating reaction.
Tollen's reagent will dry out if un-used. Also Tollen's reagent contains the complex Ag(NH3)2 OH, which is explosive when dry.