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CCEA GCE Chemistry (1110) · Unit AS 3: Basic Practical Chemistry
Mini-Lesson

AS 3: Basic Practical Chemistry

Unit AS 3 is where the theory has to survive contact with a burette. It assesses your practical skills: volumetric analysis, gravimetric analysis, calorimetry and qualitative testing.

The examinable skill is not just doing the experiment — it is justifying every step, quantifying the uncertainty and judging whether the conclusion is actually supported by the numbers.

Work through each screen, answer the questions as you go (several are full A-level calculations) and collect ⭐ stars. Press Start when you're ready.

Volumetric analysis

Making a standard solution

A standard solution has an accurately known concentration. The routine:

  • Weigh the solid accurately on a balance (weighing by difference removes the error from solid left in the weighing boat).
  • Dissolve it fully in a small volume of distilled water in a beaker.
  • Transfer to a volumetric flask, and rinse the beaker and stirring rod into the flask — otherwise some solute is left behind and the concentration is too low.
  • Make up to the graduation mark, with the bottom of the meniscus on the line, at eye level. Stopper and invert to mix thoroughly.
c = n ÷ Vand n = m ÷ M — so m = c × V × M
Calculate

Your turn — calculation 1

1Calculate the mass of anhydrous sodium carbonate, Na₂CO₃ (M = 106.0), needed to make 250 cm³ of a 0.100 mol dm⁻³ standard solution. Give your answer to 3 significant figures.
g
Hint: n = 0.100 × 0.250 = 0.0250 mol. mass = n × M.
Method

n = c × V = 0.100 × 0.250 = 0.0250 mol. mass = 0.0250 × 106.0 = 2.65 g.

Volumetric analysis

Titration technique — and why each step matters

  • Rinse the burette with the solution it will hold. Water left inside would dilute it, so a larger volume would be needed and the titre would be too high.
  • Rinse the pipette with the solution it will deliver, for the same reason.
  • The conical flask may be rinsed with distilled water — extra water changes the volume but not the moles of substance being titrated, so it has no effect on the titre.
  • Run a rough titration, then repeat carefully, adding dropwise near the end-point.
  • Take the mean of concordant titres only — within 0.10 cm³ of each other. Never include the rough titration or an anomaly.

Choosing an indicator: the colour change must fall entirely within the vertical section of the titration curve. Strong acid–strong base: either works. Strong acid–weak base (e.g. HCl with Na₂CO₃): methyl orange. Weak acid–strong base (e.g. ethanoic acid with NaOH): phenolphthalein.

Calculate

Your turn — calculation 2

225.0 cm³ of 0.100 mol dm⁻³ Na₂CO₃ is titrated against HCl. The mean titre is 22.50 cm³. Na₂CO₃ + 2HCl → 2NaCl + H₂O + CO₂. Calculate the concentration of the HCl in mol dm⁻³, to 3 significant figures.
mol dm⁻³
Hint: n(Na₂CO₃) = 0.0250 × 0.100 = 2.50 × 10⁻³ mol. The ratio is 1 : 2, so n(HCl) = 5.00 × 10⁻³. Then c = n ÷ 0.0225.
Method

n(Na₂CO₃) = 2.50 × 10⁻³ mol → n(HCl) = 2 × 2.50 × 10⁻³ = 5.00 × 10⁻³ mol. c = 5.00 × 10⁻³ ÷ 0.02250 = 0.222 mol dm⁻³.

Calculate

Your turn — calculation 3

3Titres recorded: 23.15, 23.10, 23.60 and 23.20 cm³. Calculate the mean of the concordant titres, in cm³, to 2 decimal places.
cm³
Hint: Concordant means within 0.10 cm³. 23.60 is an anomaly — leave it out.
Method

Concordant titres are 23.15, 23.10 and 23.20 (spread 0.10 cm³). Mean = (23.15 + 23.10 + 23.20) ÷ 3 = 69.45 ÷ 3 = 23.15 cm³.

Quick check

Think it through

?Why is a burette used for the acid rather than a 25 cm³ measuring cylinder?
Uncertainty

Quantifying the uncertainty in your result

% uncertainty = (uncertainty ÷ measured value) × 100
  • A burette reads to ±0.05 cm³. A titre needs two readings, so its uncertainty is ±0.10 cm³.
  • A thermometer reading to ±0.5 °C gives an uncertainty of ±1.0 °C in ΔT.
  • When values are multiplied or divided, add the percentage uncertainties.

Precise is not the same as accurate. Three titres agreeing to 0.05 cm³ are highly precise. If the burette is miscalibrated, they can all be equally wrong. Repeating reduces random error; only fixing the method removes a systematic one.

Calculate

Your turn — calculation 4

4A burette reading has an uncertainty of ±0.05 cm³. Calculate the percentage uncertainty in a titre of 22.50 cm³, to 2 decimal places.
%
Hint: Two readings → ±0.10 cm³. (0.10 ÷ 22.50) × 100.
Method

Uncertainty in the titre = 2 × 0.05 = ±0.10 cm³. (0.10 ÷ 22.50) × 100 = 0.44%. A larger titre would reduce this — one reason a 25 cm³ aliquot is chosen to give a titre near 25 cm³.

Gravimetric analysis

Water of crystallisation and heating to constant mass

Heating a hydrated salt drives off the water of crystallisation. Comparing the masses before and after gives the formula:

CuSO₄·5H₂O(s) → CuSO₄(s) + 5H₂O(g)blue crystals → white anhydrous powder
  • Weigh the crucible, then the crucible + hydrated salt.
  • Heat gently, cool in a desiccator, and re-weigh.
  • Repeat until two consecutive masses agreeheating to constant mass proves all the water has gone.

Two systematic errors to name: heating too strongly can decompose the anhydrous salt (giving a mass loss that is too large); cooling in open air lets the hygroscopic anhydrous solid reabsorb water (giving a mass loss that is too small). A desiccator solves the second.

Calculate

Your turn — calculation 5

52.50 g of hydrated copper(II) sulfate, CuSO₄·5H₂O (M = 249.6), is heated to constant mass. Calculate the mass of anhydrous CuSO₄ (M = 159.6) that should remain, to 3 significant figures.
g
Hint: n(CuSO₄·5H₂O) = 2.50 ÷ 249.6. The ratio is 1 : 1, so n(CuSO₄) is the same. mass = n × 159.6.
Method

n = 2.50 ÷ 249.6 = 0.01002 mol. mass of CuSO₄ = 0.01002 × 159.6 = 1.60 g. The mass lost as water is 2.50 − 1.60 = 0.90 g, which is 0.0501 mol — five times the moles of salt, confirming the ·5H₂O.

Qualitative analysis

Tests for cations, anions and gases

Cations

  • Flame tests — Li⁺ crimson · Na⁺ yellow · K⁺ lilac · Ca²⁺ brick-red · Cu²⁺ blue-green.
  • NH₄⁺ — warm with NaOH(aq): ammonia is released, turning damp red litmus blue.

Anions

  • Carbonate — add dilute acid: effervescence, and the CO₂ turns limewater milky.
  • Sulfate — acidify with dilute HCl, then add BaCl₂(aq): a white precipitate of BaSO₄.
  • Halides — acidify with dilute HNO₃, then add AgNO₃(aq): Cl⁻ white, Br⁻ cream, I⁻ yellow. Confirm with ammonia: AgCl dissolves in dilute NH₃, AgBr only in concentrated NH₃, AgI in neither.

Gases — O₂ relights a glowing splint · H₂ gives a squeaky pop · CO₂ turns limewater milky · NH₃ turns damp red litmus blue · Cl₂ bleaches damp litmus.

Order matters. Test for carbonate first, then sulfate, then halide. Carbonate would give a precipitate with Ba²⁺ (BaCO₃ is white) and with Ag⁺, so it must be removed by acidifying first — and that acid must be the right one: use dilute HNO₃ before AgNO₃, never HCl, or you will precipitate AgCl from the acid itself.

Sort it

What is being tested for?

Tap a test result, then tap what kind of species it identifies.

🔵 A cation

🟡 An anion

💨 A gas

Quick check

Think it through

?Before testing for a halide with silver nitrate, the solution is acidified. Which acid must be used, and why?
Match it

Match the apparatus to its purpose

Tap a piece of apparatus on the left, then its purpose on the right.

Apparatus
Purpose
Quick check

Think it through

?A student rinses the conical flask with distilled water before adding the aliquot from the pipette. What effect does this have on the titre?
Quick check

Think it through

?In a calorimetry experiment the measured enthalpy change is consistently less exothermic than the data book value. Which improvement addresses the cause?
Quick check

Think it through

?Why is a hydrated salt heated to constant mass rather than for a fixed time?
Recap

The big ideas to know

Standard solution: weigh by difference, dissolve, rinse the beaker into the volumetric flask, make up to the mark at eye level

Titration: rinse the burette and pipette with their own solution; the conical flask may be wet; use concordant titres (within 0.10 cm³) only

Indicators: methyl orange for strong acid–weak base; phenolphthalein for weak acid–strong base

Uncertainty: % uncertainty = (uncertainty ÷ value) × 100; two readings double it; add percentages when multiplying

Gravimetric: heat to constant mass; cool in a desiccator

Qualitative: carbonate → sulfate → halide, in that order; acidify with HNO₃ before AgNO₃

Error: repeating reduces random error only — a systematic error needs the method fixed

That is Unit AS 3 — the practical skills, and the reasoning behind every step. Press Finish to see your score.

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