🧊Colligative Properties Calculator - Freezing Point Depression, Boiling Point Elevation & Osmotic Pressure
Colligative properties depend only on how many solute particles are dissolved, not on what they are. The four equations are freezing point depression ΔTf = i·Kf·m and boiling point elevation ΔTb = i·Kb·m (m = molality in mol/kg), osmotic pressure Π = i·M·R·T (M = molarity) and Raoult’s law P = x(solvent)·P°. The van ’t Hoff factor i is the number of particles per formula unit: 1 for sugar or glucose, 2 for NaCl, 3 for CaCl₂, 5 for Al₂(SO₄)₃. A 1 mol/kg NaCl solution in water therefore has ΔTf = 2 × 1.86 × 1 = 3.72 °C and freezes near −3.72 °C, and a 0.1 M glucose solution at 25 °C has Π = 0.1 × 0.082057 × 298.15 ≈ 2.45 atm. The calculator has Kf, Kb, normal freezing and boiling points and 25 °C vapour pressures for water, benzene, cyclohexane, camphor, acetic acid, ethanol, carbon tetrachloride, chloroform, naphthalene, phenol, nitrobenzene, diethyl ether and acetone. Type a formula and it recognises strong electrolytes (salts, strong acids and bases), giving the ideal i and the molar mass, which you can override with a measured i. Each equation can be solved for any unknown: ΔT from concentration, the mass of solute needed for a target temperature (antifreeze, road salt), the molar mass of an unknown from measured ΔTf, ΔTb, Π or vapour pressure (the classic lab experiment, the Rast camphor method, polymer osmometry), or i from experimental data. A compare tab ranks several solutions by i·m to answer “which has the lowest freezing point” questions.
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How to use Colligative Properties Calculator
- 1Choose freezing point, boiling point, osmotic pressure, vapour pressure or compare, or click an example
- 2Pick the solvent, type the solute formula (i and molar mass are filled in), choose what to solve for and enter the known values
- 3Read the result with step-by-step working and copy the numbers you need
FAQ
- How do I find the van ’t Hoff factor i?
- Ideally i equals the number of ions one formula unit releases: 1 for non-electrolytes (glucose, sucrose, urea), 2 for NaCl or KNO₃, 3 for CaCl₂ or Na₂SO₄, 4 for FeCl₃ or K₃PO₄ and 5 for Al₂(SO₄)₃. Real solutions show ion pairing, so measured values are lower — about 1.9 for NaCl and 1.3 for MgSO₄ at 0.05 mol/kg — and the gap grows with concentration.
- How do you calculate molar mass from freezing point depression?
- Dissolve a mass w of solute in a mass W of solvent and measure ΔTf. Then m = ΔTf / (i·Kf), moles n = m × W (in kg), and molar mass M = w / n. For example, 2.00 g of an unknown in 25.0 g of benzene lowers the freezing point by 2.05 °C: m = 2.05 / 5.12 = 0.400 mol/kg, n = 0.0100 mol and M ≈ 200 g/mol. Camphor’s large Kf (about 37.7) makes it useful for tiny samples.
- Why is osmotic pressure used for proteins and polymers?
- Large molecules give very few particles per gram, so the freezing point drops by only thousandths of a degree, while the osmotic pressure is still easy to measure. A solution of 1.00 g of protein in 100 mL at 25 °C with Π = 1.85 mmHg gives c ≈ 9.95×10⁻⁵ mol/L and M ≈ 1.0×10⁵ g/mol.
- Which solution has the lowest freezing point?
- In the same solvent, compare the total particle concentration i·m: the larger it is, the lower the freezing point, the higher the boiling point and the larger the osmotic pressure. Among 0.25 m glucose (i·m = 0.25), 0.10 m NaCl (0.20), 0.08 m CaCl₂ (0.24) and 0.03 m Al₂(SO₄)₃ (0.15), the glucose solution freezes lowest. If a question gives measured i values, use those instead.