Which of the following compounds will give a silver mirror with ammoniacal silver nitrate?
Statements: (A) Formic Acid (B) Formaldehyde (C) Benzaldehyde (D) Acetone
Find the number of correct statement(s).
Which of the following compounds will give a silver mirror with ammoniacal silver nitrate?
Statements: (A) Formic Acid (B) Formaldehyde (C) Benzaldehyde (D) Acetone
Find the number of correct statement(s).
Correct answer:3
Standard Method
Given: We must identify which of the listed compounds give a silver mirror with ammoniacal silver nitrate, that is, Tollens' reagent.
Find: The correct option(s).
Tollens' reagent is used to identify aldehydes. Aldehydes are oxidized to carboxylic acids, while silver ion is reduced to metallic silver, producing the silver mirror.
From the solution analysis:
Therefore, the compounds that give a silver mirror are A, B, and C only.
There is a discrepancy between the listed answer key and the extracted solution working. The solution clearly concludes that the correct answer is A, B, and C.
Compound-wise Analysis
Given: The compounds are Formic acid, Formaldehyde, Benzaldehyde, and Acetone.
Find: Which of these respond positively to Tollens' reagent.
Tollens' test is a test for aldehydes, and formic acid is a known exception.
Hence, Formic acid, Formaldehyde, and Benzaldehyde give the test.
So the correct answer is A,B,C.
Assuming that only aldehydes give Tollens' test is incomplete. Formic acid is an important exception and also gives a silver mirror. Always check for standard exceptions.
Confusing ketones with aldehydes leads to choosing acetone. Ketones generally do not react with Tollens' reagent because they are not oxidized easily under these conditions.
Relying only on the raw marked answer without checking the solution can be misleading here. The extracted solution clearly states that A, B, and C give the silver mirror test.
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