AQA GCSE Chemistry coverage

Chemical analysis

Section 4.8
14 spec leafs

Notes and three levels of exam-style practice for each registered specification leaf in this section.

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4.8.1.1

Pure substances

  • In chemistry, a pure substance contains one element or one compound and is not mixed with another substance.
  • Test purity by measuring a melting point or boiling point and comparing it with reliable reference data.
  • For example, a sample that melts sharply at the accepted melting point is consistent with a pure substance; a mixture usually changes the value and melts over a range.
  • A common error is to use the everyday meaning of pure, such as natural or unadulterated, instead of the chemical meaning.

Tier 1 · Easy

2 marks
ORIGINAL

A sealed sample contains only solid sulfur. Decide whether it is a pure substance in the chemical sense and justify your decision.

Tier 2 · Standard

3 marks
ORIGINAL

Reference data give the melting point of substance P as 64C64\,^\circ\mathrm{C}. Batch A melts sharply at 64C64\,^\circ\mathrm{C}, while batch B melts from 5858 to 61C61\,^\circ\mathrm{C}. Which batch is more likely to be pure? Explain.

Tier 3 · Hard

4 marks
ORIGINAL

A drink is advertised as 'pure fruit juice'. Analysis shows water, sugars, acids and flavour compounds. Explain why the label may be reasonable in everyday language but the drink is not pure in chemistry.

4.8.1.2

Formulations

  • A formulation is a mixture designed to be a useful product, with every component included for a particular purpose.
  • Make a formulation by measuring and mixing its components carefully so the final product has the required properties.
  • For example, a paint may contain a pigment for colour, a solvent to control flow and a binder that leaves a solid coating.
  • A common error is to call every mixture a formulation; a formulation must have a designed use and controlled composition.

Tier 1 · Easy

2 marks
ORIGINAL

A cleaning spray is made from measured amounts of solvent, detergent, fragrance and dye, each with a stated purpose. State why the spray is a formulation.

Tier 2 · Standard

4 marks
ORIGINAL

A 250g250\,\mathrm{g} fertiliser formulation is 18%18\% nitrogen compound, 12%12\% potassium compound and the remainder filler. Calculate the mass of filler and explain one purpose of measuring the components accurately.

Tier 3 · Hard

4 marks
ORIGINAL

Two batches of a medical cream contain the same chemicals. In batch X the components were weighed precisely; in batch Y their proportions varied. Evaluate which batch better fits the definition of a formulation.

4.8.1.3

Chromatography

  • Chromatography separates a mixture because its substances distribute differently between a stationary phase and a mobile phase; a mixture may give several spots, while a pure compound gives one spot in every solvent.
  • For paper chromatography, draw a pencil origin line, add small sample spots, keep the solvent below the line, allow the solvent to rise, then mark the solvent front.
  • Calculate Rf=distance moved by the centre of the spotdistance moved by the solvent frontR_f=\frac{\text{distance moved by the centre of the spot}}{\text{distance moved by the solvent front}}; for example, 3.6/6.0=0.603.6/6.0=0.60.
  • A common error is to measure from the paper edge or spot boundary instead of from the origin to the centre of the spot.

Tier 1 · Easy

2 marks
ORIGINAL

On a chromatogram, a pigment centre is 4.2cm4.2\,\mathrm{cm} above the origin and the solvent front is 7.0cm7.0\,\mathrm{cm} above the origin. Calculate the pigment's RfR_f value.

Tier 2 · Standard

5 marks
ORIGINAL

Describe how to use paper chromatography to find out whether a purple pen ink contains more than one soluble dye. Include two setup details that prevent misleading results.

Tier 3 · Hard

5 marks
ORIGINAL

A solvent front moves 8.0cm8.0\,\mathrm{cm}. An unknown gives spots at 2.4cm2.4\,\mathrm{cm} and 5.6cm5.6\,\mathrm{cm}. Reference RfR_f values in this solvent are: J 0.300.30, K 0.550.55, L 0.700.70. Identify the substances present and state why this evidence does not prove the sample contains only those substances.

4.8.2.1

Test for hydrogen

  • Hydrogen is identified by the characteristic pop produced when it burns rapidly.
  • Hold a burning splint at the open end of the test tube containing the collected gas.
  • For example, a gas that gives a pop with a lit splint has a positive hydrogen-test result.
  • A common error is to insert a glowing splint; that is the test for oxygen, not hydrogen.

Tier 1 · Easy

1 mark
ORIGINAL

A colourless gas makes a pop when tested at the mouth of its tube with a lit splint. Identify the gas.

Tier 2 · Standard

2 marks
ORIGINAL

Give the procedure and positive observation for confirming that gas collected from a metal-acid reaction is hydrogen.

Tier 3 · Hard

3 marks
ORIGINAL

A student tests a gas using a glowing splint and sees no change, then concludes that hydrogen is absent. Evaluate the conclusion and describe the correct confirmation test.

4.8.2.2

Test for oxygen

  • Oxygen supports combustion and is identified when a glowing splint relights.
  • Insert a glowing wooden splint into the test tube containing the gas.
  • For example, a splint with no flame that bursts back into flame gives a positive oxygen result.
  • A common error is to use a burning splint and look for a pop, which tests for hydrogen.

Tier 1 · Easy

1 mark
ORIGINAL

A glowing splint returns to flame inside a jar of colourless gas. Name the gas.

Tier 2 · Standard

2 marks
ORIGINAL

Describe a test that distinguishes oxygen from a gas that does not support combustion. State the positive result.

Tier 3 · Hard

4 marks
ORIGINAL

Three observations are reported for one gas: a lit splint gives no pop, limewater stays clear, and a glowing splint relights. Use all three results to identify the gas and explain which observation is decisive.

4.8.2.3

Test for carbon dioxide

  • Carbon dioxide is identified because it forms a fine white precipitate in limewater, making the liquid look milky or cloudy.
  • Bubble the gas through, or shake it with, aqueous calcium hydroxide solution.
  • For example, clear limewater becoming cloudy is a positive result for carbon dioxide under this test.
  • A common error is to report that limewater becomes colourless; the required observation is that it turns milky or cloudy.

Tier 1 · Easy

1 mark
ORIGINAL

An unknown gas is shaken with clear limewater, which becomes cloudy. Identify the gas.

Tier 2 · Standard

2 marks
ORIGINAL

State the reagent and the expected visible change when testing a gas sample for carbon dioxide.

Tier 3 · Hard

3 marks
ORIGINAL

A learner writes: 'Carbon dioxide is confirmed because it extinguishes a flame.' Improve this claim to give the specification test, its reagent and its positive observation.

4.8.2.4

Test for chlorine

  • Chlorine gas bleaches damp litmus paper white.
  • Expose damp litmus paper to the gas while using appropriate small-scale safety precautions because chlorine is toxic.
  • For example, litmus losing all its colour and becoming white is the positive chlorine result.
  • A common error is to use dry litmus paper; moisture is required for the specified test.

Tier 1 · Easy

1 mark
ORIGINAL

Damp litmus paper loses its colour and becomes white in an unknown gas. Identify the gas.

Tier 2 · Standard

2 marks
ORIGINAL

Describe how litmus paper is used to test for chlorine and state the observation that confirms a positive result.

Tier 3 · Hard

3 marks
ORIGINAL

Two students test the same gas. One uses dry blue litmus and sees no change; the other uses damp litmus and it turns white. Explain which result should be used and what conclusion follows.

4.8.3.1

Flame tests (chemistry only)

  • Flame tests identify some metal ions: Li<sup>+</sup> crimson, Na<sup>+</sup> yellow, K<sup>+</sup> lilac, Ca<sup>2+</sup> orange-red and Cu<sup>2+</sup> green.
  • Place a small amount of a clean sample into a non-luminous flame and compare the observed colour with the known colours.
  • For example, a lilac flame indicates potassium ions, whereas an orange-red flame indicates calcium ions.
  • A common error is to treat a flame test as reliable for every mixture; a strong colour, especially sodium yellow, can mask another ion.

Tier 1 · Easy

1 mark
ORIGINAL

A compound produces a crimson flame. Identify the metal ion present.

Tier 2 · Standard

2 marks
ORIGINAL

Samples M and N give a green flame and an orange-red flame respectively. Identify the metal ion in each sample.

Tier 3 · Hard

3 marks
ORIGINAL

A mixture known to contain two metal ions gives only an intense yellow flame. State one ion supported by the observation and explain why the second ion cannot be identified confidently from this test alone.

4.8.3.2

Metal hydroxides (chemistry only)

  • With sodium hydroxide, Cu<sup>2+</sup> gives a blue precipitate, Fe<sup>2+</sup> green and Fe<sup>3+</sup> brown.
  • Add sodium hydroxide solution dropwise, record any precipitate, then add excess when distinguishing aluminium from other white precipitates.
  • Al<sup>3+</sup>, Ca<sup>2+</sup> and Mg<sup>2+</sup> form white hydroxide precipitates, but only aluminium hydroxide dissolves in excess sodium hydroxide.
  • A common error is to claim every white precipitate dissolves in excess; calcium and magnesium hydroxides remain.

Tier 1 · Easy

1 mark
ORIGINAL

Adding sodium hydroxide solution to an unknown ionic solution forms a brown precipitate. Identify the metal ion.

Tier 2 · Standard

4 marks
ORIGINAL

Solutions A and B each form a white precipitate when a little sodium hydroxide is added. The precipitate from A dissolves after excess sodium hydroxide is added, but B's remains. What can be concluded about A, and why is B not fully identified?

Tier 3 · Hard

3 marks
ORIGINAL

Three solutions are tested with sodium hydroxide. W gives a blue precipitate, X gives a green precipitate, and Y gives a white precipitate that dissolves in excess sodium hydroxide. Identify the metal ion in W, X and Y.

4.8.3.3

Carbonates (chemistry only)

  • Carbonate ions are tested by adding a dilute acid; a carbonate reacts to release carbon dioxide gas.
  • Pass the gas produced into limewater to confirm that it is carbon dioxide.
  • For example, effervescence followed by limewater turning cloudy is a positive sequence for carbonate ions.
  • A common error is to identify a carbonate from fizzing alone; the gas should be confirmed with limewater.

Tier 1 · Easy

1 mark
ORIGINAL

A solid fizzes when dilute acid is added, and the gas makes limewater cloudy. Name the ion detected in the solid.

Tier 2 · Standard

3 marks
ORIGINAL

Describe a complete chemical test for carbonate ions in an unknown powder, including how the gaseous product is identified.

Tier 3 · Hard

4 marks
ORIGINAL

Powders C and D both fizz when dilute acid is added. The gas from C turns limewater cloudy, but the gas from D leaves limewater clear. Explain which powder has tested positive for carbonate ions and why fizzing alone is insufficient evidence.

4.8.3.4

Halides (chemistry only)

  • Halide ions are tested by acidifying the solution with dilute nitric acid and then adding silver nitrate solution.
  • Use clean samples and record the precipitate colour: chloride white, bromide cream and iodide yellow.
  • For example, a cream silver-halide precipitate identifies bromide ions under the specified test conditions.
  • A common error is to swap the cream and yellow results: silver bromide is cream, while silver iodide is yellow.

Tier 1 · Easy

1 mark
ORIGINAL

After dilute nitric acid and silver nitrate are added to a solution, a yellow precipitate forms. Identify the halide ion.

Tier 2 · Standard

3 marks
ORIGINAL

Give the reagents, in order, used to test an aqueous sample for halide ions, and state the result for chloride ions.

Tier 3 · Hard

5 marks
ORIGINAL

Samples R, S and T form white, cream and yellow precipitates respectively after the correct halide test. Identify all three ions and state the two reagents that must have been added, in order.

4.8.3.5

Sulfates (chemistry only)

  • Sulfate ions form a white precipitate when barium chloride solution is added under acidic conditions.
  • Acidify the sample with dilute hydrochloric acid, then add barium chloride solution and observe any precipitate.
  • For example, a white barium sulfate precipitate is the positive result for sulfate ions.
  • A common error is to report only that the mixture turns white without naming the formation of a precipitate.

Tier 1 · Easy

1 mark
ORIGINAL

An acidified solution forms a white precipitate when barium chloride solution is added. Identify the ion being tested.

Tier 2 · Standard

3 marks
ORIGINAL

Describe the reagent sequence and positive observation for testing an unknown solution for sulfate ions.

Tier 3 · Hard

4 marks
ORIGINAL

A student adds barium chloride directly to an unknown solution, sees a white precipitate and reports sulfate ions. Evaluate the procedure and give the complete test needed before accepting the identification.

4.8.3.6

Instrumental methods (chemistry only)

  • Instrumental methods detect and identify elements or compounds using measured signals rather than only visible chemical-test observations.
  • Choose an instrumental method when rapid analysis, high sensitivity or accurate measurement is important.
  • For example, a sensitive instrument can detect a component at a concentration too low to give a clear precipitate or colour change.
  • A common error is to list 'easy' as a specification advantage; the required comparison is that instrumental methods are accurate, sensitive and rapid.

Tier 1 · Easy

1 mark
ORIGINAL

State one advantage of an instrumental method over a chemical test based on a visible colour change.

Tier 2 · Standard

2 marks
ORIGINAL

A laboratory must screen 180180 water samples in one day for a contaminant present at very low concentration. Give two reasons for choosing an instrumental method.

Tier 3 · Hard

4 marks
ORIGINAL

For a certified 10.0mgdm310.0\,\mathrm{mg\,dm^{-3}} standard, method A reports 12mgdm312\,\mathrm{mg\,dm^{-3}} after 2525 minutes and misses very dilute samples. Method B reports 10.1mgdm310.1\,\mathrm{mg\,dm^{-3}} after 4040 seconds and detects every sample. Compare the methods using the three specification advantages of instrumental analysis.

4.8.3.7

Flame emission spectroscopy (chemistry only)

  • In flame emission spectroscopy, a solution sample enters a flame and the emitted light passes through a spectroscope.
  • Identify metal ions by comparing the positions of lines in the sample spectrum with a reference set recorded in the same form.
  • Line intensity can be compared with calibration data to measure concentration; for example, an intensity halfway between two standards gives an intermediate concentration when the calibration is linear.
  • A common error is to use line brightness to identify the ion; line position identifies the ion, while intensity is used for concentration.

Tier 1 · Easy

1 mark
ORIGINAL

Reference lines occur at 589nm589\,\mathrm{nm} for sodium and 671nm671\,\mathrm{nm} for lithium. A sample has one line at 671nm671\,\mathrm{nm}. Identify the metal ion.

Tier 2 · Standard

3 marks
ORIGINAL

A sodium calibration is linear through the origin. An intensity of 2424 units corresponds to 3.0mgdm33.0\,\mathrm{mg\,dm^{-3}}. A sample gives 4040 units under identical conditions. Calculate its sodium-ion concentration.

Tier 3 · Hard

5 marks
ORIGINAL

A solution produces emission lines at 589nm589\,\mathrm{nm} and 766nm766\,\mathrm{nm}. References assign these to sodium and potassium. At 766nm766\,\mathrm{nm}, standards of 2.02.0 and 6.0mgdm36.0\,\mathrm{mg\,dm^{-3}} give intensities 1515 and 4747 units; the sample gives 3131 units. Identify both ions and estimate the potassium-ion concentration, assuming a linear response.