Question:

Which of the following compounds on reaction with ammonical silver nitrate solution forms precipitate of silver?

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Ammoniacal silver nitrate is just the formal chemical name for Tollens' reagent! Always remember: Aldehydes (compounds ending in "-al" like Ethanal) give a positive silver mirror result instantly!
Updated On: Jun 3, 2026
  • Ethanal
  • Ethanoic acid
  • Ethanol
  • Ethoxy ethane
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The Correct Option is A

Solution and Explanation

Step 1: Understanding the Question:
The question asks to identify the compound that reduces ammoniacal silver nitrate solution (Tollens' reagent) to yield a solid shiny precipitate of elemental silver (the classic silver mirror test).

Step 2: Detailed Explanation:
Ammoniacal silver nitrate solution acts as Tollens' reagent, which is a mild oxidizing agent. This reagent reacts selectively with aldehydes. Aldehydes are easily oxidized into their corresponding carboxylate anions, and in turn, they reduce the silver complex ions ($\text{[Ag(NH}_3)_2]^+$) down to metallic silver metal atoms that coat the inner walls of the vessel: $$ \text{R-CHO} + 2[\text{Ag(NH}_3)_2]^+ + 3\text{OH}^- \longrightarrow \text{R-COO}^- + 2\text{Ag}_{(s)}\downarrow + 4\text{NH}_3 + 2\text{H}_2\text{O} $$ Among the given choices:

Ethanal ($\text{CH}_3\text{CHO}$) is an aldehyde, so it gives a positive Tollens' test.

• Ethanoic acid (carboxylic acid), Ethanol (alcohol), and Ethoxy ethane (ether) are resistant to oxidation by Tollens' reagent and will not produce a silver precipitate.


Step 3: Final Answer: The compound that forms a silver precipitate upon reacting with ammoniacal silver nitrate is Ethanal, which corresponds to option (A).
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