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Class 12 Chemistry Notes

Solutions Class 12 Chemistry Notes

Complete, exam-ready notes on solutions: concentration units, Henry's and Raoult's laws, ideal and non-ideal solutions, colligative properties, osmosis and colloidal state — written for CBSE boards, JEE and NEET revision.

Class12SubjectChemistryCoversCBSE · JEE · NEET

Written byDeep Narayan· Science & Mathematics EducatorReviewed byPushpanjali

What is a solution in one line?

A solution is a homogeneous mixture of two or more substances — a solute dissolved uniformly in a solvent — whose composition can vary within certain limits and whose particles are of molecular or ionic size (below 1 nm).

Types of Solutions and Concentration Terms

Solution

A homogeneous mixture of solute and solvent. Depending on the physical state of solute and solvent, solutions can be solid-liquid (most common), liquid-liquid, gas-liquid, solid-solid, etc.

  • Molarity (M):\text{Molarity (M)}:
  • moles of solute per litre of solution.
  • Molality (m):\text{Molality (m)}:
  • moles of solute per kg of solvent (temperature independent).
  • Mole fraction (x):\text{Mole fraction (x)}:
  • ratio of moles of one component to total moles.
  • Mass percentage:\text{Mass percentage}:
  • mass of solute per 100 units of solution mass.
  • Parts per million (ppm):\text{Parts per million (ppm)}:
  • used for very dilute solutions.
M=nsoluteVsolution(L),m=nsolutewsolvent(kg),xi=nintotalM = \frac{n_{\text{solute}}}{V_{\text{solution}}(L)},\quad m = \frac{n_{\text{solute}}}{w_{\text{solvent}}(kg)},\quad x_i = \frac{n_i}{n_{\text{total}}}
Key concentration terms

Molarity vs molality

Molarity changes with temperature because volume changes; molality is temperature independent because it uses mass of solvent. Mock exams love asking which is temperature-independent.

Henry's Law and Solubility

Henry's law

p=kHxp = k_H\,x

The partial pressure of a gas in equilibrium with a solution is proportional to the mole fraction of the gas dissolved in the solution. kHk_H is the Henry's law constant (larger the kHk_H, lower the solubility of that gas).

  • Applications: carbonated drinks, oxygen in blood foams, anaesthesia using gases.
  • Effervescence on opening a soda bottle — pressure reduces, gas escapes.
  • Solubility of gases in liquids generally decreases with rising temperature.

Vapour Pressure and Raoult's Law

Raoult's law

p1=x1p1p_1 = x_1\,p_1^{\circ}

For a volatile solute, the partial vapour pressure of each component in the solution is proportional to its mole fraction times its vapour pressure in the pure state. Total pressure is the sum of partial pressures.

  • Ideal solution:\text{Ideal solution}:
  • obeys Raoult's law at all compositions with
  • ΔHmix=0\Delta H_{\text{mix}}=0
  • and
  • ΔVmix=0\Delta V_{\text{mix}}=0
  • .
  • Non-ideal (+ve deviation):\text{Non-ideal (+ve deviation)}:
  • weaker A-B interaction — vapour pressure higher than ideal.
  • Non-ideal (-ve deviation):\text{Non-ideal (-ve deviation)}:
  • stronger A-B interaction — vapour pressure lower than ideal.

Azeotropes

Azeotropes are mixtures that distil at constant composition. Minimum-boiling azeotropes show +ve deviation (e.g. ethanol-water); maximum-boiling azeotropes show -ve deviation (e.g. HNO₃-water).

Colligative Properties

Colligative properties depend only on the number of solute particles, not their nature. The four key ones are lowering of vapour pressure, boiling point elevation, freezing point depression and osmotic pressure.

  • Relative lowering of v.p.:\text{Relative lowering of v.p.}:
  • ppp=xsolute\frac{p^{\circ}-p}{p^{\circ}} = x_{\text{solute}}
  • .
  • Elevation of boiling point:\text{Elevation of boiling point}:
  • ΔTb=Kbm\Delta T_b = K_b \cdot m
  • .
  • Depression of freezing point:\text{Depression of freezing point}:
  • ΔTf=Kfm\Delta T_f = K_f \cdot m
  • .
  • Osmotic pressure:\text{Osmotic pressure}:
  • π=CRT\pi = CRT
  • .
ΔTb=Kbm,ΔTf=Kfm,π=CRT=iMRT\Delta T_b = K_b\,m,\quad \Delta T_f = K_f\,m,\quad \pi = CRT = iMRT
Colligative property formulas

Relative Molecular Mass and Abnormal Molar Mass

van't Hoff factor

i=observed colligative propertytheoretical colligative propertyi = \frac{\text{observed colligative property}}{\text{theoretical colligative property}}

Accounts for dissociation (i > 1) or association (i < 1) of solute. For colligative properties, replace the molar mass term with ii times: ΔTf=iKfm\Delta T_f = i\,K_f\,m and π=iCRT\pi = i\,CRT.

Relationship with degree of dissociation

For dissociation: i=1+(n1)αi = 1 + (n-1)\alpha. For association: i=1(11n)αi = 1 - (1 - \frac{1}{n})\alpha, where α\alpha is the degree of dissociation or association and nn is the number of particles.

Colloidal State

A colloid is a heterogeneous system of two phases — a dispersed phase (particles 1–1000 nm) and a dispersion medium. Colloids show the Tyndall effect and Brownian motion and carry charges on their particles.

  • Lyophilic:\text{Lyophilic}:
  • solvent-loving colloids that are reversible (e.g. gum, starch).
  • Lyophobic:\text{Lyophobic}:
  • solvent-hating colloids that are irreversible (e.g. metal sols).
  • Coagulation of a colloid occurs by adding an electrolyte that neutralises the particle charge.
  • Gold number and Hardy-Schulze rule describe coagulation effectiveness.

Solved Examples

Example: The freezing point of a 0.5 m aqueous solution of a non-electrolyte is depressed by 0.93 °C. Given Kf=1.86K kg mol1K_f = 1.86\,\text{K kg mol}^{-1}, find the van't Hoff factor.

Solution: ΔTf=iKfm0.93=i×1.86×0.5i=1\Delta T_f = i\,K_f\,m \Rightarrow 0.93 = i \times 1.86 \times 0.5 \Rightarrow i = 1. The observed depression matches the theoretical value, so the solute neither dissociates nor associates.

Revision

Key formulas at a glance

Memorise these before attempting numericals — most exam questions hinge on one of them.

Molarity

M=nV(L)M = \frac{n}{V(L)}

Molality

m=nwsolvent(kg)m = \frac{n}{w_{\text{solvent}}(kg)}

Mole fraction

xi=nintotalx_i = \frac{n_i}{n_{\text{total}}}

Henry's law

p=kHxp = k_H\,x

Raoult's law

p1=x1p1p_1 = x_1\,p_1^{\circ}

Elevation of B.P.

ΔTb=Kbm\Delta T_b = K_b\,m

Depression of F.P.

ΔTf=Kfm\Delta T_f = K_f\,m

Osmotic pressure

π=CRT\pi = CRT

van't Hoff factor

i=observedtheoreticali = \frac{\text{observed}}{\text{theoretical}}

Exam tips

How this chapter is asked

Where this topic appears in CBSE, JEE Main and NEET papers.

  • Molality is temperature-independent; molarity is not.
  • Solubility of gases decreases with increasing temperature.
  • Raoult's law is obeyed by ideal solutions at all compositions.
  • van't Hoff factor i = 1 + (n-1)α for dissociation.
  • Colligative properties depend on number of particles, not their nature.

FAQ

Common questions

Why is molality preferred over molarity?

Molality uses the mass of solvent, which does not change with temperature, whereas molarity uses volume, which expands on heating. So molality is temperature independent.

What is an ideal solution?

An ideal solution obeys Raoult's law at all concentrations, with zero enthalpy of mixing and zero volume change on mixing (e.g. benzene + toluene).

What is the Tyndall effect?

The scattering of light by colloidal particles, making the beam visible. It is a characteristic property of colloids, not true solutions.

What is osmotic pressure?

The excess pressure that must be applied to a solution to prevent the inward flow of solvent across a semipermeable membrane. It is a colligative property given by π = CRT.

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