Acid-Base Titration Calculator

Calculate titre volume, equivalence point, and concentration

Solve for unknown concentration at the equivalence point of an acid-base titration using the equivalents balance, with stoichiometry, equivalence pH, and an indicator suggestion. For analytical chemistry, QC, and teaching labs. It runs free in your browser on Gera Tools, with nothing uploaded.

Last updated Source: Gera Tools

What is the equivalence point in a titration?

The equivalence point is where the moles of titrant exactly neutralise the moles of analyte, accounting for stoichiometry. It is a property of the chemistry, whereas the endpoint is where your indicator changes colour. A well-chosen indicator makes the two coincide.

An acid-base titration finds an unknown concentration by reacting a measured sample with a titrant of known strength until neutralisation is complete. The volume of titrant needed, the titre, is the single measurement that unlocks the answer. This calculator turns that titre into a concentration and tells you what to expect at the endpoint.

How it works

Neutralisation is complete when the reactive equivalents of acid and base are equal. In normality form:

Ca x Va x za  =  Cb x Vb x zb

where C is molarity, V is volume, and z is the number of reactive protons or hydroxides per molecule. Rearranging for the analyte concentration:

Ca  =  (Cb x Vb x zb) / (za x Va)

The valence terms za and zb matter for polyprotic acids such as sulfuric acid (z = 2) and polyhydroxide bases such as calcium hydroxide. For a simple monoprotic-monohydroxide reaction both are 1 and the formula collapses to the familiar Ca·Va = Cb·Vb.

Equivalence pH and indicator choice

The pH at the equivalence point depends on the salt that forms. A strong acid neutralised by a strong base leaves a neutral salt, so the pH is 7. A weak acid neutralised by a strong base leaves a conjugate base, pushing the equivalence pH above 7, while a strong acid neutralised by a weak base leaves a conjugate acid and an equivalence pH below 7. Pick an indicator whose transition range brackets that pH so the colour change marks true neutralisation.

Common indicators and their transition ranges:

IndicatorTransition rangeSuitable for
Methyl orangepH 3.1–4.4Strong acid / weak base
Methyl redpH 4.4–6.2Strong acid / weak base
Bromothymol bluepH 6.0–7.6Strong acid / strong base
PhenolphthaleinpH 8.2–10.0Weak acid / strong base
Alizarin yellowpH 10.1–12.0Very weak acid / strong base

Worked example

Titrating 25.0 mL of an unknown acid against 0.100 mol/L NaOH that requires a 25.0 mL titre, with both valences 1:

Ca = (0.100 × 0.025 × 1) / (1 × 0.025) = 0.100 mol/L

The equivalence point falls at approximately pH 7, so bromothymol blue is the appropriate indicator for a clean colour change.

Now consider a diprotic case: titrating 20.0 mL of sulfuric acid (za = 2) against 0.100 mol/L NaOH, requiring a 40.0 mL titre:

Ca = (0.100 × 0.040 × 1) / (2 × 0.020) = 0.100 mol/L

Both protons are accounted for through the za term. Setting za = 1 for sulfuric acid would incorrectly halve the result.

Sources of experimental error to watch for

  • Indicator over-shoot. Adding titrant too fast near the endpoint means you may reach the indicator colour change slightly beyond the true equivalence point. Add dropwise as you approach the endpoint.
  • CO2 absorption. NaOH solutions absorb atmospheric carbon dioxide over time, lowering the effective concentration. Use freshly standardised titrant and keep solutions stoppered.
  • Temperature effects. Molarity is defined at a specific temperature, and most solutions expand slightly when warm. Titrations performed at significantly different temperatures from standardisation can introduce small systematic errors.
  • Burette parallax. Read the burette meniscus at eye level to avoid parallax error, particularly at the curved bottom of the meniscus for colourless solutions.

The equivalence pH and indicator suggestion produced by this calculator are idealised guides based on the reaction type; for exact endpoint pH in buffers or with weak electrolytes you must include the salt concentration and the relevant Ka or Kb.