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neoCatalyst Labs
Lab K-3 · Acid-Base Titration
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neoCatalyst Labs · Chemistry · Free demo

Acid-Base Titration

Add base from a burette drop by drop into an acid solution. Watch the pH S-curve form in real time, identify the equivalence point, and calculate the unknown concentration.

Add base drop by drop and watch the pH curve form. Find the equivalence point in your own data.

6 acid-base pairs
~5 minutes
Lab report included
Learning Objectives
  • → Add titrant drop-by-drop from a burette and identify the equivalence point from the pH S-curve
  • → Calculate the unknown concentration of an acid using C₁V₁ = C₂V₂ stoichiometry
  • → Run replicate trials and confirm concordance (agreement within 0.20 mL) before averaging your equivalence volume
  • → Explain why equivalence point pH differs for strong acid/base vs. weak acid/base titrations
NGSS HS-PS1-7 AP Chemistry ⏱ 45 min

📖 Pre-Lab Reading — Acid-Base Titration

What Is Titration?

Titration is a technique for determining the unknown concentration of a solution by reacting it with a precisely measured volume of a solution whose concentration is known. The solution in the burette (the titrant) is added drop by drop to the solution in the flask (the analyte) until the reaction is exactly complete.

The Neutralisation Reaction Acid + Base → Salt + Water. The equivalence point is the exact moment when moles of H⁺ equal moles of OH⁻ — neither acid nor base is in excess. Everything has been converted to salt and water.

Why the pH Changes the Way It Does

This is the key question to understand. Think about what is happening to the concentration of remaining acid as you add base:

  • Early in the titration (far from equivalence): You have a large amount of acid, so adding 1 mL of base removes only a tiny fraction of the H⁺ present. The concentration barely changes, so the pH barely changes. The curve is nearly flat.
  • Near the equivalence point: Almost all the acid has been consumed. The remaining moles of H⁺ are now very small. Adding one more drop of base destroys a large fraction of what's left — so the concentration (and therefore pH) changes dramatically with each tiny addition. This is why the curve goes nearly vertical.
  • After the equivalence point: All acid is gone. Further base just adds excess OH⁻, and you are in a new, large-volume solution. Each added mL changes the OH⁻ concentration only slightly. The curve flattens out again near pH 13–14.
The short answer: The dramatic jump near the equivalence point happens because a tiny addition of base destroys the last remaining acid — switching the solution from a tiny excess of H⁺ to a tiny excess of OH⁻. That single drop can shift pH from ~4 to ~10.

Why the Equivalence Point pH Depends on the Acid Type

At the equivalence point, all the acid has reacted with all the base. But what is left in the flask is not just water — it is a salt dissolved in water. Whether that salt makes the solution acidic, neutral, or basic determines the equivalence pH.

  • Strong acid + Strong base (e.g. HCl + NaOH): The salt formed is NaCl. Neither Na⁺ nor Cl⁻ reacts with water to produce H⁺ or OH⁻. The solution is neutral — pH = 7.
  • Weak acid + Strong base (e.g. acetic acid + NaOH): The salt formed contains the conjugate base of the weak acid (e.g. CH₃COO⁻, acetate). This conjugate base is itself weakly basic — it reacts with water: CH₃COO⁻ + H₂O → CH₃COOH + OH⁻. This produces a small amount of OH⁻, making the solution basic — pH > 7 at equivalence. The weaker the acid (larger pKₐ), the more basic the equivalence point.
Remember: A weak acid's conjugate base is not neutral — it is weakly basic. So when all the weak acid has been converted to its conjugate base by the strong base, the resulting solution is basic, not neutral.

Indicators and Endpoint

A pH indicator changes colour at a specific pH range. Phenolphthalein is colourless below pH 8.2 and pink above pH 10. Because the equivalence zone (pH 7–9 for most of our titrations) falls within this range and the pH jump is very steep, a single drop carries the indicator past its colour-change point. For weak acid + strong base, the equivalence pH is above 7, so phenolphthalein is still appropriate.

The endpoint is when the indicator first permanently changes colour. The equivalence point is the exact theoretical neutralisation point. A well-executed titration makes these nearly identical.

IndicatorpH RangeColour ChangeBest For
Phenolphthalein8.2 – 10.0Colourless → PinkStrong acid + Strong base; Weak acid + Strong base
Methyl orange3.1 – 4.4Red → Orange/YellowStrong acid + Weak base
Litmus6.0 – 8.0Red → BlueGeneral use

Calculating Concentration from Titration

Once you know the equivalence volume, use the relationship that moles of acid = moles of base at equivalence:

Cacid × Vacid = Cbase × Vbase(eq)   →   Cacid = (Cbase × Vbase(eq)) / Vacid

Example: If 0.100 M NaOH required 24.8 mL to neutralise 25.0 mL of HCl, then CHCl = (0.100 × 24.8) / 25.0 = 0.0992 M. This only works for monoprotic acids (one H⁺ per molecule).

Setup Today's Titration
Step 1 Perform the Titration

Add base from the burette in small increments. Watch the pH meter and the curve forming on the graph. When you see a large pH jump, you are near the equivalence point — switch to smaller additions.

Use these buttons to add base.
HEAT 010 2030 4050 pH METER NEOCAT pH 1.00 3.00 8.87
pH
Acidic ← → Basic
02468101214
Titration Curve — pH vs Volume of Base Added
Add Base: Added: 0.0 mL  |  Remaining:
Add base from the burette. Start with 2 mL or 5 mL increments until the pH begins to rise quickly.
Course Navigator — Unit K: Acids, Bases & pH
✓ K-1 pH Scale ✓ K-2 Red Cabbage ✦ K-3 Titration

This lab completes Unit K. You've progressed from measuring pH qualitatively (K-1), to observing natural indicators (K-2), to the quantitative technique of titration (K-3). Titration forms the foundation of analytical chemistry — the next unit builds on these stoichiometry skills.