No, the Tollen's Silver Mirror Test only confirms the presence of aldehydes.
no negative
Alkenes
You can use a litmus test it will tell you if it is alkane and will tell you the PH of the alkane metal.
1)Bromine solution in carbontetrachloride is used to identify alkanes, alkenes and alkynes. alkanes don't react therefore the color remains as it is ie, brown while alkenes and alkynes react and therfore brown color disappears. 2)Ammoniacal cuprous chloride when reacted with alkanes alkenes give no precipitate while with alkynes give red precipitate. Thus, alkanes with no reaction and unsaturation can be identified from the first test while alkynes from second test. combustion test solubility test kmno4 test sulfuric acid test
Since alcohols are obtained by hydration of alkenes, it is meaningless to manufacture alkenes from alkanes. Moreover, cracking hydrocarbons is a more effective and economical to make alkenes. Shawkat
no negative
Bromine water can test the difference between alkanes and alkenes because the bromine water turns colourless for the alkenes but doesnt change for the alkanes.
A silverish ppt. Called "silver mirror"
Alkenes
Only aldehydes give a positive Tollens test. However, under the strongly basic conditions of the test, alpha-hydroxy ketones can isomerize to aldehydes, so they will also give a positive Tollens test. Fructose is an alpha-hydroxy ketone.
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.
It is Formic acid or its anion.
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.
The principle of Tollens' test is to distinguish between aldehydes and ketones. It involves the reduction of silver ions to silver metal in the presence of aldehydes, which results in the formation of a silver mirror on the inner surface of the test tube. Ketones do not give a positive Tollens' test because they do not undergo this reaction with silver ions.
wrt
When adding the aldehyde or ketone to Tollens' reagent, the test tube is put in a warm water bath. If the reactant under test is an aldehyde, Tollens' test results in a silver mirror. If the reactant is a ketone, it will not react because a ketone cannot be oxidized easily. A ketone has no available hydrogen atom on the carbonyl carbon that can be oxidized - unlike an aldehyde, which has this hydrogen atom.
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.