Preparing Soluble Salts
Two methods for soluble salts: titration (acid + alkali) or excess solid (acid + metal/oxide/carbonate). Both end with filtration and crystallisation.
Method 1 — Titration (acid + alkali): Used when BOTH reactants are soluble (and the salt is also soluble).
- Fill burette with alkali (e.g. NaOH)
- Add known volume of acid (e.g. HCl) to conical flask; add indicator
- Titrate: add alkali slowly until indicator shows endpoint (neutralisation)
- Record volumes (titre); repeat WITHOUT indicator (indicator would contaminate product)
- Use exact volumes found → mix acid and alkali → neutralise completely
- Evaporate solution to concentrate; allow to crystallise; filter; dry
Why no indicator in the repeat? The indicator itself is a coloured organic compound that would contaminate the pure salt crystals.
Method 2 — Excess solid method (acid + insoluble metal/oxide/carbonate): Used when reactant is an insoluble solid (metal, metal oxide, metal carbonate).
- Warm acid (e.g. H₂SO₄) in a beaker
- Add excess solid (e.g. CuO) until no more dissolves and some solid remains — ensures all acid is used up (no excess acid in product)
- Filter off excess solid (removes unreacted solid and any impurities)
- Evaporate filtrate to concentrate; cool → crystals form; filter; dry at low temperature
Example: Copper(II) sulfate: CuO + H₂SO₄ → CuSO₄ + H₂O → blue crystals (CuSO₄·5H₂O) after crystallisation
- Titration: acid + alkali; use indicator to find exact volumes; repeat without indicator; crystallise.
- Excess solid: add excess metal/oxide/carbonate to acid; filter; crystallise.
- Excess solid ensures all acid used up — prevents acidic product.