Strong Acid/Base pH Calculator
Calculate pH of strong acid, strong base, and their mixtures from concentration.
Why Strong Acids Are Simple — Until They Are Not
A strong acid dissociates completely, so [H+] equals the acid concentration directly and pH follows immediately. No equilibrium calculation is needed — that is what distinguishes strong from weak.
The simplicity breaks down in two situations. First, at concentrations below about 10−6 M, water’s own autoionisation contributes comparably and cannot be ignored. Applying pH = −log C to 10−8 M HCl gives pH 8 — a basic result for an acid, which is impossible. The correct answer is about 6.98.
| [HCl] | Naive pH | Correct pH | Note |
|---|---|---|---|
| 10−2 M | 2.00 | 2.00 | Water contribution negligible |
| 10−6 M | 6.00 | 5.99 | Beginning to matter |
| 10−7 M | 7.00 | 6.79 | Water now significant |
| 10−8 M | 8.00 | 6.98 | Naive answer is impossible |
Second, at high concentration activity coefficients fall below 1, so effective concentration is less than nominal. Concentrated strong acids have a higher measured pH than the simple formula predicts.
Mixing Acid and Base
For a mixture, work in moles, not concentrations. Subtract the smaller from the larger to find the excess, then divide by the combined volume. Forgetting that the volumes add is the most common error.
Worked Examples
Common Mistakes
Below about 10−6 M, water autoionisation contributes. The formula would give pH above 7 for an acid, which is impossible — the true value approaches 7 from below.
Excess moles must be divided by the total combined volume. Using only the original acid volume overstates the concentration.
A strong base gives [OH−] directly, so calculate pOH first and subtract from 14. Applying −log to the base concentration gives pOH, not pH.
Neutral pH is 7.00 only at 25°C. At 37°C water's ionisation constant gives neutrality at about pH 6.81.
Frequently Asked Questions
Formula Explorer connections
Interpretation: This relationship connects hydrogen-ion activity, dissociation, conjugate ratios or titration stoichiometry to acid–base behavior. Assumption: Concentration approximates activity mainly in dilute solutions. Temperature, ionic strength, acid strength and equilibrium approximations affect accuracy.