pKa Calculator — Ka to pKa and Buffer pH
Enter the acid dissociation constant Ka and the concentrations of the weak acid and its conjugate base to get pKa, buffer pH (Henderson-Hasselbalch), and degree of ionisation instantly.
mol/L
mol/L
Negative log₁₀ of the acid dissociation constant
- 1
Ka (input)
0.000018 - 2
log₁₀(Ka)
log₁₀(0.000018) = -4.744727 - 3
pKa = −log₁₀(Ka)
−(-4.744727) = 4.7447
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pKa = −log₁₀(Ka). Buffer pH follows Henderson-Hasselbalch: pH = pKa + log₁₀([A⁻]/[HA]). When concentrations are equal, pH = pKa. Enter Ka and the acid/base concentrations to get pKa, buffer pH and % ionisation. Assumes ideal aqueous solution at 25 °C.
Foirmle
How this is calculated
The acid dissociation constant Ka describes how completely a weak acid HA donates a proton in water: HA ⇌ H⁺ + A⁻. Because Ka spans many orders of magnitude — roughly 10⁻¹⁵ to 10⁻¹ for common weak acids — chemists use pKa = −log₁₀(Ka), which compresses the scale to a convenient single-digit range. A lower pKa means a stronger weak acid; acetic acid has pKa ≈ 4.74, while carbonic acid (first dissociation) has pKa ≈ 6.35.
The Henderson-Hasselbalch equation pH = pKa + log₁₀([A⁻]/[HA]) predicts the pH of a buffer made from the weak acid and its conjugate base. When both concentrations are equal the log term vanishes and pH = pKa — this is the half-equivalence point of a titration and the point of maximum buffer capacity. The calculator lets you set any [A⁻]/[HA] ratio to model any buffer composition.
For % ionisation the calculator solves the exact quadratic Ka = x²/([HA] − x) rather than the common approximation x ≈ √(Ka · [HA]), so it stays accurate even when Ka/[HA] is not negligible. All results assume an ideal dilute aqueous solution at 25 °C; temperature shifts pKa (typically ±0.01–0.02 per °C for small acids), and high ionic strength changes effective Ka through activity coefficients.
Ceisteanna coitianta
Ka is the equilibrium constant for the dissociation HA ⇌ H⁺ + A⁻. Weak acids have small Ka values that are inconvenient to compare, so chemists take pKa = −log₁₀(Ka). Acetic acid: Ka ≈ 1.8×10⁻⁵, pKa ≈ 4.74. A lower pKa always means a stronger acid.
Henderson-Hasselbalch gives pH = pKa + log₁₀([A⁻]/[HA]). When [A⁻] = [HA], log₁₀(1) = 0, so pH = pKa. This is the point during a titration where exactly half the acid has been neutralised, and it is also where the buffer resists pH change most effectively.
Yes. For a base with Kb, compute pKb = −log₁₀(Kb). In water at 25 °C, pKa + pKb = 14 (the pKw of water), so you can convert directly: pKa = 14 − pKb.
Ar a dtugtar freisin
TG we-Calculate Editorial Team. (2026). pKa Calculator — Ka to pKa and Buffer pH [Online calculator]. TG we-Calculate. https://we-calculate.com/ga/calculator/pka-calculator
TG we-Calculate Editorial Team. "pKa Calculator — Ka to pKa and Buffer pH." TG we-Calculate. 2026. https://we-calculate.com/ga/calculator/pka-calculator.
TG we-Calculate Editorial Team, "pKa Calculator — Ka to pKa and Buffer pH," TG we-Calculate, 2026. [Online]. Available: https://we-calculate.com/ga/calculator/pka-calculator
@misc{wecalculate_pka_calculator, title = {pKa Calculator — Ka to pKa and Buffer pH}, author = {{TG we-Calculate Editorial Team}}, howpublished = {\url{https://we-calculate.com/ga/calculator/pka-calculator}}, year = {2026}, note = {TG we-Calculate} }
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