Carbon compounds, particularly ethanol () and ethanoic acid (
), are crucial in both industrial and domestic applications. Ethanol is widely known for its use in alcoholic beverages, as a solvent, and as a biofuel, while ethanoic acid, also known as acetic acid, is the main component of vinegar and is used in various chemical and food industries.
Ethanol (C₂H₅OH)
Physical Properties of Ethanol:
- State: Liquid at room temperature.
- Boiling Point: 78°C.
- Density: 0.789 g/cm³ (at 20°C).
- Solubility: Ethanol is completely miscible with water and many organic solvents.
- Volatility: Ethanol evaporates quickly due to its relatively low boiling point.
Chemical Properties of Ethanol:
- Combustion: Ethanol undergoes combustion when exposed to oxygen, producing carbon dioxide, water, and heat energy. The reaction is highly exothermic.
- Application: Ethanol is used as a biofuel in some vehicles due to its clean-burning properties, producing fewer pollutants than gasoline.
- Reaction with Sodium: Ethanol reacts with sodium metal to form sodium ethoxide and hydrogen gas. This reaction demonstrates ethanol's weakly acidic nature.
- Dehydration to Form Ethene: Ethanol can be dehydrated (water is removed) when heated with concentrated sulfuric acid, producing ethene (
).
- Application: Ethene is a key raw material in the plastic industry, used to make polyethylene.
Real-Life Applications of Ethanol:
- As a Solvent: Ethanol is used as a solvent in the manufacture of perfumes, paints, and drugs.
- In Beverages: Ethanol is the active ingredient in alcoholic beverages like beer, wine, and spirits.
- Disinfectant: Ethanol is a common disinfectant and is used in hand sanitizers due to its ability to kill microorganisms.
Ethanoic Acid (CH₃COOH)
Physical Properties of Ethanoic Acid:
- State: Liquid at room temperature.
- Boiling Point: 118°C.
- Density: 1.049 g/cm³.
- Solubility: Ethanoic acid is miscible with water and other organic solvents.
- Odor: Pungent, vinegar-like smell.
Chemical Properties of Ethanoic Acid:
- Reaction with Bases: Ethanoic acid reacts with bases (such as sodium hydroxide) to form salts (like sodium ethanoate) and water.
- Application: This neutralization reaction is widely used in industrial processes and in food preservation.
- Reaction with Carbonates and Bicarbonates: Ethanoic acid reacts with carbonates (e.g., sodium carbonate) and bicarbonates (e.g., sodium bicarbonate) to produce carbon dioxide, a salt, and water.
- Application: This reaction is used in the production of baked goods, where the carbon dioxide gas helps dough rise.
- Esterification: Ethanoic acid reacts with alcohols to form esters, which are sweet-smelling compounds. In the presence of concentrated sulfuric acid, ethanoic acid reacts with ethanol to form ethyl ethanoate.
- Application: Esters are used in the production of perfumes and food flavorings.

Real-Life Applications of Ethanoic Acid:
- Vinegar: Ethanoic acid is the main ingredient in vinegar, used in cooking and food preservation.
- Cleaning Agent: It is used in household cleaners to remove limescale and other mineral deposits.
- Textile Industry: Ethanoic acid is used in the production of synthetic fibers, such as cellulose acetate.
Enhanced Visualizations
- Chemical Structure of Ethanol (
)
- Ethanol is a simple alcohol with a hydroxyl group (
) attached to a two-carbon chain.
- Ethanol is a simple alcohol with a hydroxyl group (
- Chemical Structure of Ethanoic Acid (
)
- Ethanoic acid contains a carboxyl group (
) attached to a methyl group (
).
- Ethanoic acid contains a carboxyl group (
Practice Questions with Answers
Q1: Write the balanced chemical equation for the combustion of ethanol.
- Answer:
Q2: How is ethanoic acid used in household cleaning products?
- Answer: Ethanoic acid (as vinegar) is used in household cleaners to remove mineral deposits like limescale and to clean surfaces effectively.
Q3: Explain the esterification reaction between ethanoic acid and ethanol.
- Answer: Esterification occurs when ethanoic acid reacts with ethanol in the presence of concentrated sulfuric acid, forming ethyl ethanoate (an ester) and water.






