Question

To convert \(\mathrm{CH}_{2}=\mathrm{CH}-\mathrm{CH}_{2} \mathrm{CHO}\) to \(\mathrm{CH}_{2}=\mathrm{CH}-\mathrm{CH}_{2} \mathrm{COOH}\), the best reagent will be (a) \(\mathrm{KMnO}_{4}\) (b) P.C.C. (c) \(\left[\mathrm{Ag}\left(\mathrm{NH}_{3}\right)_{2}\right] \mathrm{OH}\) (d) \(\mathrm{HIO}_{4}\)

Short answer

The best reagent is (c) \([\text{Ag}(\text{NH}_3)_2]\text{OH}\).

Step-by-step solution

Understand the Reaction Type

The conversion is from an aldehyde group (-CHO) to a carboxylic acid group (-COOH). This type of conversion is typically an oxidation reaction where the aldehyde is oxidized to a carboxylic acid.

Examine Reagent Capabilities

Analyze each reagent's ability to perform the necessary oxidation:(a) \text{KMnO}_{4} is a strong oxidizing agent often used to oxidize alcohols and aldehydes to carboxylic acids. (b) \text{P.C.C.} (Pyridinium chlorochromate) is an oxidizing agent used for oxidizing alcohols to aldehydes without further oxidation. (c) \[\text{Ag}(\text{NH}_{3})_{2}\text{OH}\] \, known as Tollens' reagent, is used to oxidize aldehydes to carboxylic acids. (d) \text{HIO}_{4} is used to cleave vicinal diols and some unsaturated carbon compounds but is not commonly used to oxidize aldehydes to carboxylic acids.

Select the Most Suitable Reagent

From the list, Tollens' reagent (c) \[\text{Ag}(\text{NH}_{3})_{2}\text{OH}\] \ is specifically designed to oxidize aldehydes to carboxylic acids, making it the best choice for this reaction. \text{KMnO}_{4} could also perform the reaction, but Tollens' reagent is more precise for this transformation.

Key concepts

Oxidation Reactions

In organic chemistry, oxidation reactions involve the gain of oxygen or the loss of hydrogen in a molecule. When we talk about oxidizing, we're essentially talking about increasing the oxidation state of a substance. This type of reaction is fundamental in the transformation of various functional groups. Oxidation reactions are crucial because they often take simple organic molecules to more complex ones, which are useful in synthetic chemistry. For instance, alcohols can be oxidized to aldehydes and further to carboxylic acids.

The role of oxidizing agents is central in these reactions. An oxidizing agent, sometimes called an oxidizer, can induce the oxidation by accepting electrons. Some common oxidizing agents include Potassium permanganate (\(\mathrm{KMnO}_{4}\)), chromic acid (\(\mathrm{H}_2\mathrm{CrO}_4\)), and hydrogen peroxide (\(\mathrm{H}_2\mathrm{O}_2\)).

These agents have different strengths and selectivities. Choosing the right one is key depending on the specific reaction and desired product. In the exercise, the objective was to oxidize an aldehyde to a carboxylic acid, a common oxidation reaction in organic synthesis.

Aldehyde to Carboxylic Acid Conversion

Aldehydes are organic compounds with a carbonyl group (\(-CHO\)) bonded to a hydrogen atom. They are usually more reactive than ketones and can undergo various transformations. One of the most common transformations is oxidation to a carboxylic acid.

The conversion of an aldehyde to a carboxylic acid involves adding an oxygen atom to the compound and turning the hydrogen atom in the aldehyde group into an -OH group of the carboxylic acid. When selecting the appropriate oxidizing agent for this conversion, preference is given to reagents that selectively oxidize aldehydes without affecting other parts of the molecule excessively.

For example, in the presented exercise, Tollens' reagent is ideal because it specifically targets the aldehyde group and converts it to a carboxylic acid effectively. Alternatives like \(\mathrm{KMnO}_{4}\) can also achieve this, but they are stronger oxidizers and may affect other reactive parts of your molecule.

Organic Reagents

Reagents are the backbone of organic chemistry reactions. They are substances or compounds added to a system to prompt a chemical reaction. Understanding the nature and function of these reagents is crucial for predicting and controlling organic reactions.

• Potassium permanganate (\(\mathrm{KMnO}_{4}\)): A strong oxidizing agent used in converting alcohols and aldehydes to carboxylic acids. Due to its strength, it should be used with caution as it can also oxidize other parts of the molecule.
• PCC (Pyridinium chlorochromate): Typically used to oxidize primary alcohols to aldehydes without further oxidation to carboxylic acids.
• Tollens' Reagent (\(\mathrm{Ag}(\mathrm{NH}_{3})_{2}\mathrm{OH}\)): Specially designed to oxidize aldehydes to carboxylic acids while minimizing changes to other functional groups in the molecule. Its selectivity makes it a favorite for this conversion.
• Periodic acid (\(\mathrm{HIO}_{4}\)): Often used for cleaving vicinal diols, this is not typically used for the oxidation of aldehydes to carboxylic acids.

In choosing a reagent, one must consider its specificity, strength, and the particular functional group needing modification in the substrate. This understanding allows for precise modifications and more efficient chemical transformations in organic synthesis.