Visualize the titration of a strong diprotic acid (e.g., H₂SO₄) with a strong base (e.g., NaOH).
This tool simulates the complete pH titration curve for a strong diprotic acid—specifically, an acid like Sulfuric Acid (H₂SO₄) that has a strong first proton and a weak second proton.
This type of titration is chemically unique and follows a different model than a typical weak diprotic acid. This simulator accurately plots the curve by solving the complex equilibrium calculations for each step of the "strong-then-weak" titration process.
Unlike weak acids, the titration of Sulfuric Acid (H₂SO₄) with a strong base (like NaOH) is a "stitched" process with two distinct phases:
pKa₁ in water. H₂SO₄ + H₂O → H₃O⁺ + HSO₄⁻ (100% complete)HSO₄⁻) is a weak acid with its own pKa value. HSO₄⁻ + H₂O ⇌ H₃O⁺ + SO₄²⁻ (This is pKa₂, which is ≈ 1.99)This "strong-then-weak" nature creates a unique curve:
-log[C]. The simulator must solve a quadratic equation for a solution containing both the H⁺ from the first dissociation and the additional H⁺ from the second dissociation.Veq₁): This point is masked or "hidden." Because the pKa₂ (1.99) is so strong, there is no sharp "jump." The curve transitions smoothly from titrating the strong H⁺ into the HSO₄⁻ / SO₄²⁻ buffer region.Veq₂): This is the only sharp, visible equivalence point in the titration. It represents the complete neutralization of the HSO₄⁻ ion into the weak base SO₄²⁻.pKa for the second proton. For Sulfuric Acid, the standard value is 1.99.You may notice that for extremely dilute solutions (e.g., 0.001 M or less), the pH at the second equivalence point (Veq₂) may be calculated as slightly acidic (e.g., pH 6.2) when the true pH is neutral or slightly basic (e.g., pH 7.07).
This is a known and expected behavior of the standard chemical models used. At such high dilutions, the resulting conjugate base (SO₄²⁻, with a pKb ≈ 12) is incredibly weak and contributes almost no OH⁻ to the solution. The simple quadratic formula used for this step does not include the autoionization of water (Kw), so it correctly shows that the base's contribution is negligible.
This result confirms the tool's chemical accuracy: it correctly identifies that at these unrealistic concentrations, the Veq₂ "jump" is so small and "squashed" by water's neutrality that it would be practically undetectable in a real lab.