Question

The fatty acid which shows reducing property is (a) ethanoic acid (b) oxalic acid (c) formic acid (d) acetic acid

Short answer

Formic acid shows reducing properties.

Step-by-step solution

Identify the required property

The question asks us to identify a fatty acid with a reducing property. Reducing properties mean that the compound can donate electrons to other molecules.

Understand fatty acids

Ethanoic acid, oxalic acid, formic acid, and acetic acid are examples of fatty acids or organic acids. Among these, formic acid (HCOOH) is the simplest carboxylic acid.

Examine the structure of formic acid

Formic acid (HCOOH) has a structure where the aldehydic hydrogen atom is directly bonded to the carbon atom of the carboxyl group. This unique structure imparts reducing properties because it resembles an aldehyde, which naturally exhibits reducing behavior.

Determine the reducing ability of formic acid

Formic acid reacts with oxidizing agents by undergoing oxidation itself, such as being oxidized to carbon dioxide while reducing other substances. This ability aligns with the properties of a reducing agent.

Conclude the choice of fatty acid with reducing property

Among the given options, formic acid (c) is the only fatty acid capable of acting as a reducing agent based on its structural characteristics.

Key concepts

Formic Acid

Formic acid, also known as methanoic acid, is the simplest carboxylic acid, with the chemical formula \( \text{HCOOH} \). It is characterized by its single carbon atom attached to both an aldehydic hydrogen and a hydroxyl group. This simple structure is what makes formic acid unique among other fatty acids.

• The carbon atom in formic acid is directly linked to a hydrogen, mimicking the structural nature of an aldehyde.
• This structural configuration allows formic acid to exhibit reducing properties, significantly different from typical carboxylic acids.

Understanding these properties underlines why formic acid can donate electrons, behaving as a reducing agent. This potential is critical in its reactions with oxidizing agents, where formic acid itself gets oxidized in the process. Its ability to undergo such transformations is the primary reason why formic acid stands out in scenarios involving reducing reactions.

Carboxylic Acids

Carboxylic acids are organic acids characterized by a carboxyl group \( (-\text{COOH}) \), which consists of a carbonyl and a hydroxyl group connected to the same carbon atom. This functional group is fundamental to their chemistry.

• Carboxylic acids are typically weak acids but play a crucial role in organic chemistry due to their versatility.
• They can participate in a wide range of chemical reactions, including reduction, oxidation, and esterification.

Owing to their structure, carboxylic acids generally do not act as reducing agents. However, formic acid is an exception because it contains an additional hydrogen atom linked directly to the carbon. This bond configuration allows formic acid to act differently compared to other carboxylic acids, lending it unique reducing properties.

Oxidizing Agents

Oxidizing agents are substances that gain electrons in chemical reactions, causing the oxidation of other substances. They themselves get reduced during this process. Many oxidizing agents interact with reducing agents like formic acid.

• An oxidizing agent accepts electrons from the reducing agent, undergoing a change of oxidation state in the process.
• Common examples include oxygen, hydrogen peroxide, and potassium permanganate.

When an oxidizing agent interacts with formic acid, formic acid donates electrons while being transformed. This electron donation causes formic acid to be oxidized, typically to carbon dioxide, exemplifying its role as a reducing agent. This interplay highlights the dual nature of redox reactions where one substance is oxidized while another is reduced.