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Carboxylic Acids Explained: Structure, Properties and Practical Applications

Introduction

Organic chemistry includes many important compounds that differ based on their functional groups. Aldehydes, ketones, and carboxylic acids are all carbonyl compounds, meaning they contain a C=O group. Aldehhydes have the general formula R–CHO, ketones are represented as R–CO–R, and carboxylic acids are written as R–COOH. Even though these compounds are related, their structures lead to very different properties and uses.


What Are Carboxylic Acids?

Carboxylic acids are organic acids that contain a carboxyl group (–COOH). One of the most familiar examples is acetic acid, commonly known as vinegar. The general formula for this group of compounds is RCOOH.

These acids occur widely in nature. Citrus fruits such as lemons and oranges contain citric acid, while lactic acid is formed during fermentation and is important in food processing. The first few members of this series include methanoic acid, ethanoic acid, and propanoic acid.


Structure of Carboxylic Acids

A carboxylic acid molecule has a central carbon atom bonded to:

  • an –OH group through a single bond,

  • an oxygen atom through a double bond,

  • and another carbon atom or hydrogen through a single bond.

This arrangement allows strong hydrogen bonding, which explains many of the physical and chemical properties of carboxylic acids.


Examples Found in Nature

Common examples include acetic acid, propanoic acid, benzoic acid, valeric acid, palmitic acid, and stearic acid. Fatty acids such as oleic acid and linoleic acid are present in plants and animals.

Many amino acids also contain a carboxyl group. Examples include histidine, leucine, lysine, valine, methionine, and tryptophan. Butanoic acid is produced in sweat glands and is responsible for certain strong odors.


Properties of Carboxylic Acids

Carboxylic acids are usually colorless and have a sour taste. Lower members of this group are liquids at room temperature, while higher members are solids. As the carbon chain length increases, boiling and melting points also increase.

Their solubility in water decreases as the size of the hydrocarbon chain grows, but they dissolve easily in organic solvents like ethanol and ether. Pure, water-free acetic acid is known as glacial acetic acid.

Chemically, carboxylic acids are weak Brønsted–Lowry acids. They can donate one proton to form a carboxylate ion (RCOO⁻). The strength of acidity depends on the attached group; for example, oxalic acid is stronger than benzoic acid.


Naming of Carboxylic Acids

Carboxylic acids are named using IUPAC rules by replacing the “-e” of the parent alkane with “-oic acid.” For instance, CH₃COOH is called ethanoic acid, while C₆H₅COOH is known as benzoic acid.

In compounds such as amino acids, the position of the amino group is shown by numbering the carbon chain from the carboxyl carbon. For example, NH₂–CH₂–CH₂–COOH is named 3-aminopropanoic acid.


Applications and Importance

The carboxylic acid uses are wide and essential in everyday life. In the food industry, acetic acid is used as a preservative. In medicine, compounds like aspirin are derived from carboxylic acids.

They are also used in the production of perfumes, artificial flavors, soaps, detergents, polymers, and adhesives. Salicylic acid is common in acne treatments, while butanoic acid is used in toothpaste, mouthwash, and cosmetics. Formic acid is important in the rubber industry for coagulating latex.

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Conclusion

Carboxylic acids are a vital group of organic compounds with unique structures, properties, and applications. Along with aldehydes and ketones, they belong to the carbonyl family, but their acidic nature makes them especially important. From food preservation and pharmaceuticals to cosmetics and polymers, carboxylic acids play a key role in modern life, with acetic acid being the most well-known example.

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