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Degree of Dissociation Calculator

Fraction of a weak electrolyte or gas that dissociates — from Ka and concentration (Ostwald’s law), from conductivity, or from the observed van’t Hoff factor / vapour density.

Method
Ka or Kb
Concentration
Molar conductivity Λ
Limiting molar conductivity Λ°
Observed van’t Hoff factor i
Particles produced per formula unit
Theoretical vapour density
Observed vapour density
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How it works

Ka = c·α² ÷ (1 − α) (→ α ≈ √(Ka/c) when small); α = Λ/Λ°; α = (i − 1)/(n − 1); α = (D₀/D − 1)/(n − 1)

The degree of dissociation is the fraction of molecules split into ions (or fragments) at equilibrium. For weak acids Ostwald’s dilution law shows it rises as the solution is diluted even though Ka is fixed — 0.1 M acetic acid is 1.3% ionised, 0.001 M is 13%. The same α governs colligative properties through the van’t Hoff factor and, for gases that dissociate on heating (PCl₅, N₂O₄), shows up as a vapour density lower than the formula predicts.

Worked example

Acetic acid, Ka = 1.8 × 10⁻⁵, 0.1 M: α = 0.0133 (1.33%), giving [H⁺] = 1.3 × 10⁻³ M and pH 2.88.

Frequently asked questions

When is √(K/c) good enough?

When α < 5%; beyond that solve the quadratic, which the calculator does.

Why is Λ/Λ° only approximate?

Ion mobility falls with concentration even without association; Debye–Hückel–Onsager corrections refine it.

Related calculators

For study and planning — check units and conditions against your data source before using a result in the lab.