Q.Write the mathematical form of Raoult's law.
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Raoult's Law: From Intuition to Precision
Imagine you have a beaker of pure water at room temperature. Some water molecules at the surface have enough energy to escape into the air above — that's vapour pressure. Now dissolve some sugar in that water. The sugar molecules take up space at the surface, blocking some water molecules from escaping. Fewer water molecules can leave the liquid per second, so the vapour pressure drops.
That's the core intuition: a non-volatile solute lowers the solvent's vapour pressure simply by getting in the way.
But what if both components can evaporate — say, a mixture of benzene and toluene? Then both kinds of molecules crowd the surface, and both contribute to the total vapour pressure. The question becomes: how much does each contribute?
The Precise Statement
For a solution of volatile liquids, Raoult's Law says:
pi=xipi∗
where:
- pi = partial vapour pressure of component i above the solution
- xi = mole fraction of component i in the liquid solution
- pi∗ = vapour pressure of pure component i at the same temperature
The law applies to each volatile component separately. The total vapour pressure above the solution is simply the sum:
Ptotal=p1+p2=x1p1∗+x2p2∗
What This Means Physically
The mole fraction xi tells you the fraction of molecules at the surface that are of type i. If half the molecules in the liquid are benzene (xbenzene=0.5), then roughly half the surface sites are occupied by benzene molecules. So the rate at which benzene escapes should be about half the rate from pure benzene — hence pbenzene=0.5×pbenzene∗.
This is a linear relationship: plot pi against xi, and you get a straight line from the origin (when xi=0, pi=0) up to pi∗ (when xi=1, pure component).
Raoult's Law is an idealisation. It works best when the two liquids are chemically similar — same type of intermolecular forces (e.g., both non-polar, or both with similar hydrogen bonding). Benzene–toluene is a classic example. When the molecules interact very differently (like ethanol and water), the law fails — that's when you get deviations from Raoult's Law.
A Concrete Example
Suppose you mix 2 moles of benzene (p∗=100 mm Hg) with 3 moles of toluene (p∗=40 mm Hg) at 25°C.
Mole fractions:
- xbenzene=2+32=0.4
- xtoluene=53=0.6
Partial pressures:
- pbenzene=0.4×100=40 mm Hg
- ptoluene=0.6×40=24 mm Hg
Total vapour pressure: 40+24=64 mm Hg
Notice: the total pressure is not a simple average of the pure pressures. It's a weighted average, with mole fractions as weights.
Why This Matters …
Raoult's law states that each volatile component's partial vapour pressure in a solution is proportional to its mole fraction, with the pure-component vapour pressure as the constant of proportionality. …
Raoult's law: for a solution of volatile liquids, each component's partial vapour pressure is proportional to its mole fraction, with the pure-component vapour pressure as the proportionality constant.
For a binary solution of two volatile liquids, components 1 and 2:
p1 = x1 . p1(deg)
p2 = x2 . p2(deg)
where p1(deg), p2(deg) are the vapour pressures of the pure components, and x1, x2 are their mole fractions in solution.
…
- CBSE 2025Set ANNUAL1 markQ.Write the mathematical form of Raoult's law.
›Reveal solutionSolution
Raoult's law: for a solution of volatile liquids, each component's partial vapour pressure is proportional to its mole fraction, with the pure-component vapour pressure as the proportionality constant.
For a binary solution of two volatile liquids, components 1 and 2:
p1 = x1 . p1(deg)
p2 = x2 . p2(deg)
where p1(deg), p2(deg) are the vapour pressures of the pure components, and x1, x2 are their mole fractions in solution.
…
- CBSE 2025Set ANNUAL1 markQ.Define Raoult's law for a solution containing a non-volatile solute.
›Reveal solutionSolution
Raoult's law states that the vapour pressure of the solvent above a solution is directly proportional to the mole fraction of the solvent present.
Statement of Raoult's law
For a solution containing a non-volatile solute, Raoult's law states: the partial vapour pressure of the solvent (p1) over the solution is directly proportional to its mole fraction (x1) in the solution.
p1∝x1⇒p1=p1∘x1
where p1∘ is the vapour pressure of the pure solvent at that temperature. Since the solute is non-volatile, it contributes nothing to the vapour pressure, so p1 IS the total vapour pressure of the solution.
…
- CBSE 2023Set ANNUAL1 markQ.State Dalton's law of partial pressure. OR What are colligative properties?
›Reveal solutionSolution
Each gas in a mixture behaves as if it alone occupies the whole container, and the individual pressures simply add up.
For a mixture of non-reacting gases at constant temperature and volume, the total pressure is the sum of the partial pressures of the individual gases: Ptotal = p₁ + p₂ + p₃ + …, where each pᵢ is the pressure that gas i would exert if it occupied the container alone at the same temperature. This principle underlies the relation used for the vapour pressure of a solution of two volatile liquids (Raoult's law): the total va …
- CBSE 2023Set ANNUAL1 markMCQQ.For a binary ideal liquid solution, the total pressure of the solution is given as -(i) P_Total = P°_A + (P°_A − P°_B) x_A(ii) P_Total = P°_B + (P°_A − P°_B) x_A(iii) P_Total = P°_B + (P°_B − P°_A) x_A(iv) P_Total = P°_A + (P°_B − P°_A) x_A
›Reveal solutionSolution
Starting from Raoult's law for each component and substituting xB=1−xA gives the total pressure as a linear function of xA.
For an ideal binary liquid solution of A and B, Raoult's law gives the partial pressure of each component as proportional to its mole fraction:
pA=xAP°A,pB=xBP°B
Total pressure: …
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