Titration Analysis: How to Find an Unknown Concentration
Master titration analysis: burette technique, equivalence point vs endpoint, indicators, and step-by-step concentration calculations with a worked example.
Quick answer
Titration analysis is a laboratory technique that finds the concentration of an unknown solution by carefully adding a solution of known concentration (the titrant) until the reaction is just complete. The volume of titrant used reveals the unknown concentration through reaction stoichiometry.
Unit: molarity (mol/L)
Example: 25.00 mL of unknown HCl is titrated with 0.100 M NaOH, and 20.00 mL of NaOH reaches the endpoint. Because HCl and NaOH react 1:1, M_HCl × 25.00 mL = 0.100 M × 20.00 mL, so the HCl concentration is 0.0800 M.
What you will learn
- Set up and perform an acid-base titration using a burette
- Distinguish the equivalence point from the endpoint
- Select an appropriate indicator for a given titration
- Calculate an unknown concentration from titration data
- Sketch and interpret a simple titration curve
What a titration does
A titration is one of the most precise tools in analytical chemistry. Instead of guessing a concentration from a quick test, you let chemistry measure itself: a solution of known concentration is added, drop by drop, to a measured volume of the unknown solution until the reaction between them is exactly complete. Because you know precisely how much reactant you added, stoichiometry tells you exactly how much was in the unknown.
The unknown solution is called the analyte, and the known solution added from the burette is the titrant. The entire technique rests on one idea — if the balanced equation tells you the mole ratio, the volumes tell you the concentration ratio.
The equipment and setup
A standard acid-base titration uses a few key pieces of glassware:
- Burette: a long graduated tube with a stopcock that delivers titrant in precisely measured volumes, readable to 0.01 mL.
- Erlenmeyer flask: holds the measured analyte; its narrow neck reduces splashing during swirling.
- Pipette: delivers an exact, known volume of the analyte into the flask.
- Indicator: a few drops of a dye that changes color at the right moment.
The procedure runs like this: pipette a known volume of analyte into the flask, add a few drops of indicator, fill the burette with titrant and record the starting level, then add titrant slowly while swirling — fast at first, then drop by drop as the color change approaches. Record the final burette reading; the difference is the titrant volume used.
Always read the burette at the bottom of the meniscus with your eye level with it. Reading from above or below (parallax) can shift the volume by several tenths of a milliliter.
Equivalence point vs endpoint
Two terms sound alike but mean different things, and the distinction is the heart of titration theory.
The equivalence point is the theoretical moment when exactly enough titrant has been added to react completely with the analyte — the stoichiometric point dictated by the balanced equation. You cannot see it directly.
The endpoint is the practical moment you actually observe: the permanent color change of the indicator. A good titration chooses an indicator whose color change happens as close as possible to the equivalence point, so the observed endpoint is an excellent stand-in for the true equivalence point.
For a strong acid titrated with a strong base, the equivalence point sits at pH 7. For a weak acid titrated with a strong base, the equivalence point is basic (pH > 7), because the conjugate base of the weak acid makes the solution slightly alkaline — so the indicator must be chosen accordingly.
Equivalence point = stoichiometric completion (theory). Endpoint = indicator color change (observation). Good technique makes them coincide.
Indicators: the color-change signal
An indicator is a weak acid or base whose two forms have different colors, and which switches form over a narrow pH range. Common choices include:
- Phenolphthalein: colorless to pink, pH 8.2–10. The classic choice for strong acid–strong base and weak acid–strong base titrations.
- Bromothymol blue: yellow to blue, pH 6.0–7.6. Useful near neutral equivalence points.
- Methyl orange: red to yellow, pH 3.1–4.4. Suited to titrations with acidic equivalence points, such as strong acid–weak base.
Only two or three drops go into the flask. The indicator is itself a chemical participant, so adding too much would consume a measurable amount of titrant and move the endpoint. The color change should be permanent — if the color fades after swirling, you have not quite reached the endpoint yet.
Doing the math: the titration calculation
Here is where the precision pays off. At the equivalence point, moles of titrant added equal moles of analyte neutralized (adjusted for the mole ratio). For the common 1:1 case, such as HCl with NaOH:
where and are the molarity and volume of the acid, and and are the molarity and volume of the base. Volumes may be in milliliters as long as both use the same unit, since the units cancel.
Worked example: 25.00 mL of HCl of unknown concentration is titrated with 0.100 M NaOH, and the endpoint arrives after 20.00 mL of NaOH.
- Write the relation:
- Solve:
For reactions that are not 1:1, such as H2SO4 with NaOH (1:2), multiply each side by its stoichiometric coefficient: , where and come from the balanced equation.
Titration curves
Plotting pH against the volume of titrant added produces a titration curve, a powerful visual summary of the reaction. A strong acid–strong base curve starts at low pH, rises very slowly, then shoots nearly vertically through the equivalence point at pH 7 before leveling off in the basic region.
That steep vertical jump is why titrations are so precise: near the equivalence point, a single drop of titrant swings the pH by several units, so the indicator's color change pinpoints the volume sharply. Weak acid–strong base curves show a gentler rise and an equivalence point above pH 7, plus a flattened buffer region where pH resists change — the same buffering behavior that keeps blood pH stable.
Beyond acid-base titrations
The drop-by-drop technique extends well beyond acids and bases:
- Redox titrations use oxidation-reduction reactions, often with indicators that change color when oxidized or reduced, to analyze substances like iron content or vitamin C.
- Complexometric titrations use chelating agents such as EDTA to measure metal ions — the standard method for determining water hardness from calcium and magnesium.
- Precipitation titrations track the formation of an insoluble solid, for example titrating chloride with silver nitrate.
Whatever the reaction type, the logic is identical: add a known solution until the chemistry is just complete, measure the volume, and let stoichiometry reveal the unknown.
Variables and units
| Symbol | Name | Unit | Meaning |
|---|---|---|---|
| acid molarity | mol/L | Molarity (concentration) of the acid analyte. | |
| acid volume | mL or L (consistent) | Volume of the acid analyte measured into the flask. | |
| base molarity | mol/L | Molarity (concentration) of the base titrant. | |
| base volume | mL or L (consistent) | Volume of the base titrant delivered from the burette. |
Common mistakes
The equivalence point is the exact stoichiometric completion of the reaction — a theoretical point. The endpoint is the observed color change of the indicator. A well-chosen indicator makes them nearly coincide, but they are different concepts.
Only a few drops are needed. Indicators are themselves weak acids or bases, so a large amount can consume a measurable quantity of titrant and shift the endpoint.
Acid-base titrations are the most common classroom type, but redox titrations, precipitation titrations, and complexometric titrations (such as EDTA titrations for water hardness) all use the same careful-addition technique.
Volumes are read from the bottom of the meniscus — the curved dip in the liquid surface — with your eye level with it, to avoid parallax error.
Real-world applications
Water treatment plants test alkalinity and hardness by titration before adjusting chemistry
Food producers measure the acidity of vinegar, dairy, and wine to verify label claims
Pharmaceutical quality control confirms the strength of drug solutions batch by batch
Environmental laboratories determine dissolved pollutants and acid rain impact in water samples
Clinical and agricultural labs analyze soil and fertilizer nutrient content
Frequently asked questions
Why must the titrant be added very slowly near the end?
Add the titrant drop by drop and swirl continuously, especially as the color change approaches. A single drop can carry the solution past the endpoint, and there is no way to undo an overshoot — you would have to start the titration over.
What is a back titration?
A back titration is used when the analyte reacts too slowly or has no good indicator. You add a known excess of a reagent that reacts with the analyte, then titrate the leftover reagent. Subtracting gives the amount that reacted with the analyte.
How do you choose the right indicator?
Choose an indicator whose color-change pH range brackets the equivalence-point pH of your specific titration. A strong acid–strong base titration has an equivalence pH of 7, so phenolphthalein or bromothymol blue both work; a weak acid–strong base titration has an equivalence pH above 7, so phenolphthalein is the better choice.
Why rinse the burette with titrant instead of water?
Rinse the burette with a small portion of titrant and drain it before filling. This removes water droplets clinging to the glass that would otherwise dilute your carefully prepared titrant and make its concentration slightly lower than you think.
Can reading the meniscus wrong really cause error?
Yes — reading from an angle (parallax) can shift your reading by a few tenths of a milliliter, which is significant in analytical work. Always bring your eye level with the bottom of the meniscus before recording the volume.