Ethanol (C₂H₅OH) and Ethanoic Acid (CH₃COOH)
Key Point 1: Ethanol – Physical and Chemical Properties
Physical Properties
- Ethanol is a clear, colorless, and volatile liquid.
- It has a pleasant odor and gives a burning taste if tasted (not recommended).
- Its boiling point is about 78°C, which is lower than the boiling point of water (100°C).
- Ethanol mixes with water in any proportion. This is due to hydrogen bonding.
- It is highly volatile and evaporates quickly at room temperature.
Examples:
- Laboratory Setup: If you leave a beaker of ethanol open in the lab, it will evaporate faster than water.
- Sanitizer: Most hand sanitizers contain ethanol. The cooling on your hand when sanitizer dries is due to ethanol's volatility.
- Solvent Use: Ethanol is commonly used to dissolve chemicals in the lab, such as in perfumes or medicines.
Chemical Properties
a) Reaction with Sodium
- Ethanol reacts with sodium (Na) to form sodium ethoxide and hydrogen gas.
- Equation:
Example:
- Lab Reaction: Add a small piece of sodium in ethanol – bubbles of hydrogen are seen.
- Demonstration: Bubbles rise and the solution contains sodium ethoxide.
b) Combustion
- Ethanol burns in the presence of oxygen to release carbon dioxide, water, and energy.
- Equation:
Examples:
- Spirit lamps in laboratories use ethanol as fuel; they burn with a blue flame.
- Ethanol-blended petrol ignites in engines during combustion.
c) Dehydration
- When heated with concentrated sulfuric acid, ethanol loses water to form ethene (an alkene).
- Equation:
Examples:
- Lab Activity: Heating ethanol with sulfuric acid produces a gas (ethene) that decolorizes bromine water.
- Industrial Use: This method is used in the production of ethene from ethanol.
d) Oxidation
- When oxidized with strong oxidizers such as acidic K₂Cr₂O₇ or KMnO₄, ethanol converts to ethanoic acid.
- Equation:
Examples:
- Chemical Test: Add ethanol to acidified potassium dichromate; the solution changes from orange to green, showing oxidation.
- Everyday Life: This reaction explains how alcoholic drinks turn sour.
Key Point 2: Uses of Ethanol
-
Beverages: Ethanol is the alcohol in drinks such as beer, wine, whisky.
- Example: Beer (4-8% ethanol) and Wine (about 12%).
- Example: Drinking whisky is consuming a mixture with up to 40% ethanol.
-
Fuel: Used as a fuel alone or mixed with petrol.
- Example: Ethanol-blended petrol (E10, which is 10% ethanol) reduces vehicle pollution.
- Example: Spirit lamps in laboratories.
-
Antiseptic: Ethanol is in sanitizers and wipes because it kills germs.
- Example: Hand sanitizer during the COVID-19 pandemic.
- Example: Medical swabs use ethanol to clean skin before injections.
Key Point 3: Ethanoic Acid (CH₃COOH) – Physical and Chemical Properties
Physical Properties
- Colorless liquid with a pungent, vinegar-like smell.
- Tastes sour.
- Boiling point: 118°C.
- Freezing Point: 16.7°C. Below this, it solidifies, called Glacial acetic acid.
- Highly soluble in water.
Examples:
- Kitchen Vinegar: The sour taste and smell of vinegar.
- Winter Day: Ethanoic acid forms ice-like crystals in a cold lab – students see “glacial” acetic acid.
- Dilute in Water: When you add ethanoic acid to water, no layers form—it's completely soluble.
Chemical Properties
a) Acidic Nature
- Ethanoic acid is a weak acid; it partially ionizes in water to give H⁺ ions.
- Equation:
Examples:
- Litmus Test: Blue litmus paper turns red with ethanoic acid—shows it’s acidic.
- pH Testing: Ethanoic acid solution has a pH around 3-4.
b) Reaction with Metals
- Reacts with active metals (like sodium, zinc) to give hydrogen gas.
- Equation:
Examples:
- Lab Test: Add sodium to ethanoic acid—fizzing hydrogen gas is seen.
- Real-life: Acidic foods in metal containers sometimes cause gas bubbles.
c) Reaction with Carbonates and Bicarbonates
- Produces carbon dioxide gas.
- Equation:
Examples:
- Kitchen Test: Adding vinegar (acetic acid) to baking soda (NaHCO₃) creates bubbles of CO₂.
- Cleaning: Vinegar removes lime-scale from kettles because it reacts with calcium carbonate, producing fizz.
d) Neutralization (Reaction with Base)
- Ethanoic acid reacts with bases (like NaOH) to form a salt (acetate) and water.
- Equation:
Examples:
- Lab Titration: Neutralizing vinegar with sodium hydroxide in an experiment.
- Food Preserving: Acetic acid can neutralize basic substances during food preparation.
e) Esterification
- Reacts with alcohol (like ethanol) in the presence of concentrated sulfuric acid to form an ester with a fruity smell.
- Equation:
- This produces ethyl ethanoate, which smells like pineapple.
Examples:
- Fruity Flavors: The smell of raspberry or banana essence is from esters like ethyl ethanoate.
- Classroom Experiment: Mixing ethanol and ethanoic acid with a little sulfuric acid and warming releases a sweet, fruity scent.
Key Point 4: Uses of Ethanoic Acid
-
Vinegar: A 5-8% solution of acetic acid in water is vinegar.
- Example: Used to preserve pickles.
- Example: Added to salads for taste.
-
Food Preservative: Helps in preserving foods by making the environment acidic.
- Example: Used in commercial packaged foods.
- Example: Used in pickles and chutneys at home.
-
Industrial Use: Used to manufacture chemicals, acetates, dyes, and plastics.
- Example: Cellulose acetate for making photographic films.
- Example: Sodium acetate used in heating pads.
-
Medicinal Use: Dilute solutions used as antiseptics (e.g., for ear drops).
Key Point 5: Differences between Ethanol and Ethanoic Acid
| Properties | Ethanol (C₂H₅OH) | Ethanoic Acid (CH₃COOH) |
|---|---|---|
| Nature | Alcohol | Carboxylic Acid |
| Odor | Pleasant, fruity | Pungent, vinegar-like |
| pH | Nearly neutral (about 7) | Acidic (about 3-4) |
| Taste | Burning, a bit sweet | Sour |
| Reaction with Na | Liberates H₂ (gas) | Liberates H₂ (gas) |
| Reaction with Base | No reaction | Forms salt & water |
Examples:
- Smell Test: Smell a drop of each (with caution); ethanol is pleasant, ethanoic acid is sharp and pungent.
- Litmus Paper Test: Ethanol does not change blue litmus, ethanoic acid turns blue litmus red.
- Reaction with NaOH: Ethanoic acid reacts with NaOH to form sodium acetate and water, while ethanol shows no reaction.
Activity: Action of Acetic Acid on Sodium Bicarbonate
Objective:
To test if a liquid sample is acetic acid by checking if it reacts with sodium bicarbonate to produce carbon dioxide.
Materials:
- Test tube
- Dropper
- Acetic acid (vinegar)
- Sodium bicarbonate (baking soda)
Steps:
- Take a small quantity (about 2 mL) of acetic acid in a test tube.
- Add a pinch of sodium bicarbonate to the test tube.
- Observe the reaction.
Observations:
- Effervescence (bubbles) is seen due to carbon dioxide gas.
- This confirms the acidic nature of ethanoic acid.
Explanation:
Acetic acid reacts with sodium bicarbonate forming sodium acetate, water, and carbon dioxide.
Equation:
Fun Twist:
Blow up a balloon by fitting it over the test tube before adding sodium bicarbonate. The CO₂ generated will fill the balloon!
Scenario-based Questions
Scenario 1:
You spill some sanitizer on your hand and notice it dries quickly and gives a cooling sensation.
- Question: Why does ethanol in the sanitizer evaporate so fast, and why do you feel cool?
- Answer: Ethanol is highly volatile, so it evaporates quickly. The evaporation absorbs heat from your skin, giving a cooling sensation.
Scenario 2:
Your mother adds vinegar to a salad.
- Question: What is the role of ethanoic acid in vinegar for the salad?
- Answer: Ethanoic acid gives the salad a sour taste and can act as a mild preservative by inhibiting the growth of bacteria.
Scenario 3:
In the lab, your teacher asks you to distinguish between ethanol and ethanoic acid using a chemical test.
- Question: Which test would you perform, and what would you observe?
- Answer: I would use blue litmus paper. Ethanoic acid turns it red due to its acidic nature, while ethanol does not change the color.
Scenario 4:
You want to create a fruity-smelling liquid in the lab.
- Question: Which two chemicals would you mix and what catalyst is needed?
- Answer: I would mix ethanol and ethanoic acid with a few drops of concentrated sulfuric acid as a catalyst to form ethyl ethanoate, which smells fruity....