Determine equivalence point, limiting reagent, and final pH for strong acid–strong base neutralization reactions.
⚡ Acid Equivalents: — mol
⚡ Base Equivalents: — mol
? Limiting Reagent: —
⚖️ Equivalence Status: —
? Total Volume: — L
?️ Final pH: —
The curve shows pH change as base is added. The steepest point indicates the equivalence point (calculated from 0 to 1.5×Veq).
Neutralization is the reaction between H⁺ (from acid) and OH⁻ (from base) to form water. For strong acids and bases (e.g., HCl, NaOH), the reaction goes to completion.
Core principle: At the equivalence point, moles of H⁺ = moles of OH⁻.
Ca·Va·za = Cb·Vb·zb
where z is the number of H⁺/OH⁻ per formula unit.
The final pH depends on which ion is in excess:
| Condition | Excess species | pH calculation |
|---|---|---|
| n(H⁺) = n(OH⁻) | None (neutral salt) | pH = 7.00 (at 25°C) |
| n(H⁺) > n(OH⁻) | H⁺ | [H⁺] = excess mmol / total volume (mL) → pH = -log₁₀([H⁺]) |
| n(H⁺) < n(OH⁻) | OH⁻ | [OH⁻] = excess mmol / total volume → pOH = -log₁₀([OH⁻]), pH = 14 - pOH |
* Assumes complete dissociation and neglects activity coefficients. When excess concentration is below 10⁻⁷ M, water autoionization dominates and pH is set to 7.00.
Acids like H₂SO₄ can donate 2 H⁺ (za=2); bases like Ba(OH)₂ accept 2 H⁺ (zb=2). Our calculator handles this via the acidity/basicity input. For weak polyprotic species (e.g., H₃PO₄), the first equivalence point is still governed by stoichiometry, but the pH calculation requires more advanced treatment.
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