Chemistry·Revision Notes

Colligative Properties — Revision Notes

NEET UG
Version 1Updated 22 Mar 2026

⚡ 30-Second Revision

  • RLVPP0PsP0=iXB\frac{P^0 - P_s}{P^0} = i X_B
  • EBPΔTb=iKbm\Delta T_b = i K_b m
  • DFPΔTf=iKfm\Delta T_f = i K_f m
  • OPΠ=iCRT\Pi = i CRT
  • Van't Hoff Factor ($i$)Ratio of observed to theoretical particles.

- Non-electrolyte: i=1i=1 - Electrolyte (dissociation): i1i \ge 1 - Association: i1i \le 1

  • $K_b$Ebullioscopic constant (K kg mol1^{-1})
  • $K_f$Cryoscopic constant (K kg mol1^{-1})
  • UnitsTT in Kelvin for Π\Pi, mm in mol/kg for ΔTb,ΔTf\Delta T_b, \Delta T_f, CC in mol/L for Π\Pi.

2-Minute Revision

Colligative properties are solution properties that depend on the *number* of solute particles, not their chemical identity. They are observed in dilute solutions with non-volatile solutes. The four main properties are: Relative Lowering of Vapor Pressure (RLVP), Elevation in Boiling Point (EBP), Depression in Freezing Point (DFP), and Osmotic Pressure (OP).

RLVP is the fractional decrease in vapor pressure, equal to the mole fraction of the solute (iXBiX_B). EBP (ΔTb=iKbm\Delta T_b = i K_b m) and DFP (ΔTf=iKfm\Delta T_f = i K_f m) are directly proportional to the molality (mm) of the solution, with KbK_b and KfK_f being solvent-specific constants. Osmotic Pressure (Π=iCRT\Pi = iCRT) is proportional to the molarity (CC) and absolute temperature (TT).

For electrolytes or associating solutes, the van't Hoff factor (ii) must be included. For dissociation, i>1i > 1; for association, i<1i < 1; for non-electrolytes, i=1i=1. These properties are crucial for determining molecular masses of unknown solutes and have applications in various fields, including biology and industry. Remember to convert temperature to Kelvin for osmotic pressure calculations and use molality for boiling/freezing point changes.

5-Minute Revision

Colligative properties are fundamental to understanding solution behavior. They are defined as properties that depend solely on the *number* of solute particles in a given quantity of solvent, irrespective of their chemical nature. This applies to dilute solutions containing non-volatile solutes. The four key properties are:

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  1. Relative Lowering of Vapor Pressure (RLVP)When a non-volatile solute is added, the solvent's vapor pressure decreases. Raoult's Law states P0PsP0=iXB\frac{P^0 - P_s}{P^0} = i X_B, where P0P^0 is pure solvent vapor pressure, PsP_s is solution vapor pressure, XBX_B is solute mole fraction, and ii is the van't Hoff factor.
  2. 2
  3. Elevation in Boiling Point (EBP)The solution boils at a higher temperature than the pure solvent. The elevation is ΔTb=iKbm\Delta T_b = i K_b m, where KbK_b is the ebullioscopic constant (solvent-specific) and mm is molality.
  4. 3
  5. Depression in Freezing Point (DFP)The solution freezes at a lower temperature than the pure solvent. The depression is ΔTf=iKfm\Delta T_f = i K_f m, where KfK_f is the cryoscopic constant (solvent-specific) and mm is molality.
  6. 4
  7. Osmotic Pressure (OP)The pressure required to stop the net flow of solvent across a semi-permeable membrane. The van't Hoff equation is Π=iCRT\Pi = iCRT, where CC is molarity, RR is the gas constant, and TT is absolute temperature.

**Van't Hoff Factor (ii)**: This factor accounts for the actual number of particles in solution. For non-electrolytes (e.g., glucose, urea), i=1i=1. For electrolytes, i>1i > 1 due to dissociation (e.g., NaCl i2i \approx 2, CaCl2_2 i3i \approx 3). For association (e.g., ethanoic acid in benzene), i<1i < 1. If the degree of dissociation (α\alpha) is given, i=1+(n1)αi = 1 + (n-1)\alpha, where nn is the number of ions produced. For association, i=1+(1n1)αi = 1 + (\frac{1}{n}-1)\alpha.

Key Points for NEET: Always use the van't Hoff factor. Use molality for ΔTb\Delta T_b and ΔTf\Delta T_f (temperature-independent) and molarity for Π\Pi (measured at specific temperature). Convert all temperatures to Kelvin for osmotic pressure calculations.

These properties are extensively used to determine the molecular mass of unknown solutes. For example, if 18 g of glucose (M.M. = 180 g/mol) is dissolved in 1 kg of water, m=0.1 mol/kgm = 0.1\text{ mol/kg}. If $K_f = 1.

86\text{ K kg mol}^{-1},then, then\Delta T_f = 1 \times 1.86 \times 0.1 = 0.186\text{ K}.Thesolutionfreezesat. The solution freezes at-0.186^\circ\text{C}$.

Prelims Revision Notes

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  1. DefinitionColligative properties depend *only* on the *number* of solute particles, not their nature. Solute must be non-volatile; solution must be dilute.
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  3. Four Properties & Formulas (with van't Hoff factor $i$)

* Relative Lowering of Vapor Pressure (RLVP): P0PsP0=iXB\frac{P^0 - P_s}{P^0} = i X_B * P0P^0: Vapor pressure of pure solvent. * PsP_s: Vapor pressure of solution. * XBX_B: Mole fraction of solute. * Elevation in Boiling Point (EBP): ΔTb=iKbm\Delta T_b = i K_b m * ΔTb=TbsolutionTbpure solvent\Delta T_b = T_b^{\text{solution}} - T_b^{\text{pure solvent}} * KbK_b: Ebullioscopic constant (solvent-specific, K kg mol1^{-1}).

* mm: Molality (moles of solute / kg of solvent). * Depression in Freezing Point (DFP): ΔTf=iKfm\Delta T_f = i K_f m * ΔTf=Tfpure solventTfsolution\Delta T_f = T_f^{\text{pure solvent}} - T_f^{\text{solution}} * KfK_f: Cryoscopic constant (solvent-specific, K kg mol1^{-1}).

* mm: Molality. * Osmotic Pressure (OP): Π=iCRT\Pi = i CRT * Π\Pi: Osmotic pressure (atm or Pa). * CC: Molarity (moles of solute / L of solution). * RR: Gas constant (0.0821 L atm mol1 K10.0821\text{ L atm mol}^{-1}\text{ K}^{-1} or $8.

314\text{ J mol}^{-1}\text{ K}^{-1}).). *T$: Absolute temperature (Kelvin).

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  1. Van't Hoff Factor ($i$)Accounts for dissociation/association.

* Non-electrolytes (glucose, urea): i=1i=1. * Electrolytes (NaCl, CaCl2_2): i>1i > 1. For complete dissociation, i=number of ionsi = \text{number of ions}. * Association (ethanoic acid in benzene): i<1i < 1. * Degree of dissociation (α\alpha): i=1+(n1)αi = 1 + (n-1)\alpha. * Degree of association (α\alpha): i=1+(1n1)αi = 1 + (\frac{1}{n}-1)\alpha.

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  1. Molecular Mass DeterminationAll colligative properties can be used to find the molecular mass of an unknown non-volatile solute. Osmotic pressure is best for macromolecules.
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  3. Important ConversionsTemperature to Kelvin for Π\Pi calculations. Mass of solvent to kg for molality. Volume of solution to L for molarity.
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  5. Comparison of SolutionsTo compare colligative properties, compare the product i×mi \times m (or i×Ci \times C). Higher i×mi \times m means greater ΔTb\Delta T_b, greater ΔTf\Delta T_f (thus lower freezing point), and greater Π\Pi.

Vyyuha Quick Recall

To remember the four colligative properties and their dependence: Really Easy Determination Of Molecular Mass.

  • RLVP (Relative Lowering of Vapor Pressure) \rightarrow Mole fraction (XBX_B)
  • EBP (Elevation in Boiling Point) \rightarrow Molality (mm)
  • DFP (Depression in Freezing Point) \rightarrow Molality (mm)
  • OP (Osmotic Pressure) \rightarrow Molarity (CC)

And don't forget the 'i' factor for electrolytes: 'I' for Ions!

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