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IGCSE Chemistry: Cambridge 0620 tutoring, Malaysia

Experimental Techniques: IGCSE Chemistry Exam Guide

How to answer experimental techniques questions in IGCSE Chemistry 0620. Separation methods, purity, chromatography and measuring instruments.

Published by IGCSEChemistry.com.my

Chemistry teaching team: K. S. Tan (15+ years teaching IGCSE Chemistry) and Ms Yash (10+ years teaching IGCSE Chemistry) and Ms Kartini (15+ years teaching IGCSE Chemistry).

Mapped to Cambridge IGCSE Chemistry 0620 (2026–2028). Last updated 2026-08-19.

Experimental techniques is the first topic in the 0620 syllabus and one of the most practical. Questions appear on Papers 2 and 4 (choosing and describing separation methods) and Paper 6 (designing and evaluating experiments). The topic rewards precise vocabulary and clear procedural descriptions. The full content is under experimental techniques.

Separation methods: choosing and describing

The exam sets two types of question. The first asks you to choose the correct method for a given mixture. The second asks you to describe the method step by step.

How to choose

MixtureWhat you wantMethod
Sand in waterThe sand or the waterFiltration
Salt dissolved in waterThe saltEvaporation / crystallisation
Salt dissolved in waterThe pure waterSimple distillation
Ethanol and waterBoth, separatelyFractional distillation
Oil and waterBoth, separatelySeparating funnel
Dyes in inkIdentify the componentsChromatography
Copper sulfate crystals from solutionLarge, pure crystalsCrystallisation (slow evaporation)

How to describe (the marks)

When the question says “describe how you would…” it expects a step-by-step method. Each step is typically worth one mark. Include:

  • The name of the equipment (filter funnel, evaporating basin, condenser, etc.).
  • The specific action (pour the mixture through filter paper, heat gently, collect the distillate).
  • How you know the process is complete (residue remains on filter paper, crystals start to form when a glass rod is dipped in, distillate stops collecting).

Distillation detail

Simple distillation is tested more often than fractional, and the marks come from knowing the apparatus:

  1. Heat the solution in a flask.
  2. The liquid with the lower boiling point evaporates first.
  3. The vapour passes into the condenser, where cold water flows around the outside.
  4. The vapour condenses back to liquid and is collected in a beaker at the end.

The condenser requires cold water flowing in at the bottom and out at the top (counter-current). This detail is tested on Paper 6 apparatus questions.

Fractional distillation

Used when two or more miscible liquids have different boiling points. The fractionating column provides a temperature gradient: the liquid with the lower boiling point reaches the top first and passes into the condenser.

The exam asks how fractional distillation separates crude oil into fractions. Each fraction contains hydrocarbons with similar boiling points. Shorter-chain hydrocarbons have lower boiling points and are collected at the top; longer-chain hydrocarbons have higher boiling points and are collected at the bottom.

Chromatography

Paper chromatography separates components of a mixture based on their different solubilities in the solvent.

The procedure

  1. Draw a pencil baseline near the bottom of the chromatography paper (pencil, not ink, because ink would run).
  2. Place a small spot of the mixture on the baseline.
  3. Place the paper in the solvent so the solvent level is below the baseline.
  4. Allow the solvent to rise up the paper by capillary action.
  5. Remove the paper when the solvent front nears the top and mark the solvent front immediately.

Interpreting chromatograms

  • Each spot represents a different substance.
  • If a spot in the mixture lines up with a spot of a known substance, they are the same substance.
  • The Rf value identifies a substance: Rf = distance moved by substance / distance moved by solvent front.
  • A pure substance gives a single spot. An impure substance gives multiple spots.

Common errors

  • Using pen instead of pencil for the baseline (the ink runs and contaminates the result).
  • Not stating that the solvent level must be below the baseline (otherwise the spots dissolve directly into the solvent).
  • Measuring Rf from the wrong point (always measure from the baseline, not from the bottom of the paper).

Purity and melting point

A pure substance has a sharp melting point that matches the data book value. An impure substance:

  • Melts over a range of temperatures (not a sharp point).
  • Melts at a temperature lower than the expected melting point.

The exam may give you a table of melting points for several substances and ask you to identify which is impure (the one with a range or a depressed value).

Measuring instruments and accuracy

Paper 6 frequently tests whether you can choose the right measuring instrument and read it accurately.

MeasurementInstrumentPrecision
Volume of liquid (rough)Measuring cylinder1 cm3 or 0.5 cm3
Volume of liquid (precise)Burette0.05 cm3
MassBalance0.01 g or 0.1 g
TemperatureThermometer0.5 C or 1 C
TimeStopwatch0.01 s

Read the meniscus at eye level for liquid measurements. The meniscus curves downward for water; read from the bottom of the curve.

More detail on Paper 6 specific techniques is in the Paper 6 guide.

Worked exam question

Q (Paper 4): A student has a mixture of sand and salt. Describe how the student could obtain a sample of pure, dry salt from this mixture. (4 marks)

Model answer:

  1. Add water to the mixture and stir to dissolve the salt (1).
  2. Filter the mixture through filter paper in a funnel to remove the insoluble sand (1).
  3. Heat the filtrate gently in an evaporating basin to evaporate some of the water (1).
  4. Allow the remaining solution to cool and crystallise, then pat the crystals dry with filter paper (1).

Each step earns one mark. Missing “add water to dissolve” at the start is the most common error, because students jump straight to filtering without dissolving the salt first.

Experimental techniques questions are among the most mark-accessible on the paper because they test procedure rather than deep understanding. If these marks are being lost, the issue is usually imprecise descriptions rather than missing knowledge. A trial lesson can sharpen the procedural language quickly.

Frequently asked questions

What separation methods do I need for 0620?

Filtration (insoluble solid from liquid), evaporation and crystallisation (dissolved solid from solution), simple distillation (liquid from solution, collecting the liquid), fractional distillation (separating miscible liquids with different boiling points), chromatography (separating and identifying components of a mixture), and use of a separating funnel (immiscible liquids).

How do I choose the right separation method?

Identify what you want to keep and what the mixture contains. Insoluble solid in a liquid: filter. Dissolved solid in water (you want the solid): evaporate and crystallise. Dissolved solid in water (you want the pure water): distil. Two miscible liquids: fractional distillation. Identifying dyes or pigments: chromatography. Two immiscible liquids: separating funnel.

How do I calculate Rf values in chromatography?

Rf = distance travelled by the substance / distance travelled by the solvent front. Measure from the baseline (pencil line where the spot was placed) to the centre of the spot, and from the baseline to the solvent front. The Rf value is always less than 1 and has no units.

What does the melting point tell you about the purity of a substance?

A pure substance has a sharp, fixed melting point. An impure substance melts over a range and at a lower temperature than the pure substance. If the question gives you a melting point range or a melting point lower than the data book value, the substance is impure.

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