🔹 1. Definition of Carboxylic Acids
- Carboxylic acids are a group of organic compounds that contain the carboxyl functional group:
–COOH. - General formula: CnH2n+1COOH
- The carboxyl group is made up of a carbonyl group (C=O) and a hydroxyl group (–OH) attached to the same carbon atom.
Example:
- Methanoic acid: HCOOH
- Ethanoic acid: CH₃COOH
🔹 2. General Properties of Carboxylic Acids
Physical Properties:
- Have sharp, sour smells (like vinegar).
- Soluble in water (small-chain acids), forming acidic solutions.
- Have higher boiling points due to hydrogen bonding between molecules.
Chemical Properties:
- They behave as weak acids.
- They release hydrogen ions (H⁺) in water.
- Show typical acidic reactions, forming salts.
🔹 3. Reactions of Carboxylic Acids
Carboxylic acids react with metals, metal oxides, carbonates, hydrogen carbonates, and alcohols.
🔸 a) With Metals
Reaction Type: Acid + Metal → Salt + Hydrogen gas
Example:
Ethanoic acid + Magnesium → Magnesium ethanoate + Hydrogen2CH₃COOH + Mg → (CH₃COO)₂Mg + H₂
🔹 Observation: Effervescence (bubbles of hydrogen gas)
🔸 b) With Metal Oxides
Reaction Type: Acid + Metal Oxide → Salt + Water
Example:
Ethanoic acid + Copper(II) oxide → Copper(II) ethanoate + Water2CH₃COOH + CuO → (CH₃COO)₂Cu + H₂O
🔸 c) With Metal Carbonates
Reaction Type: Acid + Carbonate → Salt + Water + Carbon dioxide
Example:
Ethanoic acid + Calcium carbonate → Calcium ethanoate + Water + CO₂2CH₃COOH + CaCO₃ → (CH₃COO)₂Ca + H₂O + CO₂
🔹 Observation: Effervescence due to CO₂ gas, turns limewater milky
🔸 d) With Metal Hydrogen Carbonates
Reaction Type: Acid + Hydrogen Carbonate → Salt + Water + CO₂
Example:
Ethanoic acid + Sodium hydrogen carbonate → Sodium ethanoate + Water + CO₂CH₃COOH + NaHCO₃ → CH₃COONa + H₂O + CO₂
🔸 e) With Alcohols – Esterification Reaction
🔹 4. Detailed: Esterification Reaction
- Carboxylic acid reacts with alcohol in presence of a strong acid catalyst (usually concentrated sulfuric acid) to form an ester and water.
General Equation:
Carboxylic acid + Alcohol ⇌ Ester + Water
(equilibrium reaction)
Example:
Ethanoic acid + Ethanol ⇌ Ethyl ethanoate + WaterCH₃COOH + CH₃CH₂OH ⇌ CH₃COOCH₂CH₃ + H₂O
🧪 Conditions:
- Catalyst: Concentrated H₂SO₄
- Heating under reflux
🔹 Esters have sweet, fruity smells.
🔹 5. Uses of Esters
Esters are widely used due to their pleasant smells and chemical properties:
- Perfumes and fragrances
- Food flavourings (like banana essence, pineapple flavour)
- Solvents for paints and nail polish
- Plasticisers in making flexible plastics
📝 Summary Table
| Reaction Type | Reactants | Products | Observation |
|---|---|---|---|
| With Metals | Carboxylic acid + Metal | Salt + H₂ | Bubbles (hydrogen gas) |
| With Metal Oxides | Carboxylic acid + Metal oxide | Salt + H₂O | Solid dissolves |
| With Carbonates | Carboxylic acid + Carbonate | Salt + H₂O + CO₂ | Effervescence, limewater test |
| With Hydrogen Carbonates | Carboxylic acid + NaHCO₃ | Salt + H₂O + CO₂ | Effervescence |
| Esterification | Carboxylic acid + Alcohol | Ester + Water | Sweet smell after heating |
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