\(\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{CH}=\mathrm{CHCHO} \rightarrow \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{CH}=\mathrm{CHCOOH}\) The best oxidizing agent that can be used for the above conversion is (a) acidified \(\mathrm{KMnO}_{4}\) solution (b) Tollens' reagent (c) \(\mathrm{SeO}_{2}\) in \(\mathrm{AcOH}\) (d) all the above

Short Answer

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a) Acidified \(\mathrm{KMnO}_{4}\) solution b) Tollens' reagent c) \(\mathrm{SeO}_{2}\) in \(\mathrm{AcOH}\) d) All the above Answer: d) All the above

Step by step solution

01

Analyze the oxidizing agent (a) - acidified \(\mathrm{KMnO}_{4}\) solution

Acidified potassium permanganate (\(\mathrm{KMnO}_{4}\)) is a strong oxidizing agent and can easily oxidize aldehydes to carboxylic acids. Therefore, this can be a suitable option to perform the given reaction.
02

Analyze the oxidizing agent (b) - Tollens' reagent

Tollens' reagent is a relatively mild oxidizing agent primarily used to distinguish aldehydes from ketones. This reagent selectively oxidizes aldehydes to carboxylic acids, but it doesn't affect C=C double bonds. Hence, this can be a suitable option to perform the given reaction without affecting the C=C double bond.
03

Analyze the oxidizing agent (c) - \(\mathrm{SeO}_{2}\) in \(\mathrm{AcOH}\)

Selenium dioxide (\(\mathrm{SeO}_{2}\)) in acetic acid (\(\mathrm{AcOH}\)) is a selective oxidizing agent that can oxidize aldehydes to their corresponding carboxylic acids. This reagent is also selective in its action and doesn't affect C=C double bonds. Therefore, this can be a suitable option to perform the given reaction.
04

Analyze the oxidizing agent (d) - all the above

Since all the mentioned oxidizing agents are suitable for performing the given reaction, option (d) - all the above, is the correct answer. All the mentioned agents can oxidize the aldehyde compound to a carboxylic acid compound without affecting the C=C double bond.

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