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SACE Stage 2 Chemistry exam strategy: The 2026 guide

SACEChemistryStudy guide13 min read

How the 2026 SACE Stage 2 Chemistry exam works: a 130-minute paper worth 30 percent covering all four topics, the data sheet you receive, what the investigation and knowledge criteria reward, worked calculations in the exam style (pH, Kc, calorimetry, concentration units), common mistakes and a plan to 4 November.

Jump to a section
  1. The exam at a glance
  2. What the criteria reward
  3. The four topics
  4. Worked calculations in the exam style
  5. Command words
  6. Common mistakes
  7. Six weeks to 4 November

The exam at a glance

2026 SACE Stage 2 Chemistry exam

Wednesday 4 November 2026, 9 am (South Australian time). A 130-minute external examination worth 30 percent of your subject result, covering science inquiry skills and all four topics. You receive a data sheet with a periodic table, SI prefixes, symbols of common quantities, some mathematical relationships and a table of the relative activities of metals.

The format comes from the SACE Stage 2 Chemistry subject outline, and the date and duration from the SACE Board's 2026 examinations timetable. The timetable notes that some subjects have additional reading time, with instructions sent to schools at the start of Term 4.

How your grade is built: investigations folio 30 percent, skills and applications tasks 40 percent, exam 30 percent.

What the criteria reward

All specific features of both assessment design criteria may be assessed in the exam.

  • Investigation, analysis and evaluation: designing investigations (IAE1), obtaining and representing data (IAE2), analysing and interpreting data to justify conclusions (IAE3), and evaluating procedures and their effect on data (IAE4).
  • Knowledge and application: understanding chemical concepts (KA1), applying them in new and familiar contexts (KA2), science and society (KA3), and communicating with correct terms, equations and representations (KA4).

In Chemistry, KA4 means balanced equations with states, correct structural formulas and IUPAC names, and correct units and significant figures.

The four topics

Topic Exam favourites
1. Monitoring the environment Greenhouse gases and ocean acidification (with pH), photochemical smog and catalytic converters, concentration units and titrations, chromatography (Rf and retention times), electron configurations and atomic absorption spectroscopy
2. Managing chemical processes Rate graphs and collision theory, energy profile diagrams, Kc expressions and calculations, Le Châtelier's principle, industrial compromise and flow charts
3. Organic and biological chemistry Alcohols, aldehydes and ketones, carbohydrates, carboxylic acids, amines, esters, amides, triglycerides and proteins
4. Managing resources Fuels, biofuels and enthalpy, fuel cells and hydrogen, water treatment, soil chemistry, polymers, metal extraction, electrolysis and recycling

The topics deep dive works through all four topics and links every dot point on the site.

Worked calculations in the exam style

Ocean pH (Topic 1)

Seawater has [H+]=7.9×10−9[\text{H}^+] = 7.9 \times 10^{-9} mol L−1^{-1}. Find its pH and explain how rising atmospheric carbon dioxide changes it.

pH=−log⁡(7.9×10−9)=8.10\text{pH} = -\log(7.9 \times 10^{-9}) = 8.10.

CO2(aq)+H2O(l)⇌H2CO3(aq)⇌H+(aq)+HCO3−(aq)\text{CO}_2(aq) + \text{H}_2\text{O}(l) \rightleftharpoons \text{H}_2\text{CO}_3(aq) \rightleftharpoons \text{H}^+(aq) + \text{HCO}_3^-(aq)

More dissolved CO2\text{CO}_2 shifts these equilibria to the right, increasing [H+][\text{H}^+] and lowering the pH. The extra H+\text{H}^+ reacts with carbonate ions (H++CO32−→HCO3−\text{H}^+ + \text{CO}_3^{2-} \rightarrow \text{HCO}_3^-), making less carbonate available for shells and favouring the dissolution of calcium carbonate.

Kc from initial and equilibrium quantities (Topic 2)

1.00 mol of N2O4\text{N}_2\text{O}_4 is placed in a sealed 2.00 L flask: N2O4(g)⇌2NO2(g)\text{N}_2\text{O}_4(g) \rightleftharpoons 2\text{NO}_2(g). At equilibrium, 0.40 mol of NO2\text{NO}_2 is present. Calculate Kc.

N2O4\text{N}_2\text{O}_4 NO2\text{NO}_2
Initial (mol) 1.00 0
Change (mol) −0.20-0.20 +0.40+0.40
Equilibrium (mol) 0.80 0.40
Equilibrium (mol L−1^{-1}) 0.40 0.20

Kc=[NO2]2[N2O4]=(0.20)20.40=0.10K_c = \frac{[\text{NO}_2]^2}{[\text{N}_2\text{O}_4]} = \frac{(0.20)^2}{0.40} = 0.10

Convert moles to concentrations before substituting, and use the mole ratio (1 : 2) for the change row.

Calorimetry and fuel comparison (Topic 4)

Burning 0.50 g of ethanol (M=46.07M = 46.07 g mol−1^{-1}) raises the temperature of 200 g of water by 15.0 °C. Estimate the molar enthalpy of combustion.

q=mcΔT=200×4.18×15.0=12 540q = mc\Delta T = 200 \times 4.18 \times 15.0 = 12\,540 J =12.5= 12.5 kJ. n(ethanol)=0.5046.07=0.0109n(\text{ethanol}) = \dfrac{0.50}{46.07} = 0.0109 mol.

ΔH≈−12.50.0109≈−1.16×103\Delta H \approx -\dfrac{12.5}{0.0109} \approx -1.16 \times 10^3 kJ mol−1^{-1}.

The accepted value is about −1367-1367 kJ mol−1^{-1}; the experimental value is smaller in magnitude because heat is lost to the surroundings and combustion may be incomplete, a systematic error worth naming in an evaluation question. Per gram, the accepted value is 1367÷46.07≈29.71367 \div 46.07 \approx 29.7 kJ g−1^{-1}.

Concentration units (Topic 1)

A water sample contains 25 mg of nitrate ions per litre. Express this in ppm and in mol L−1^{-1} (M(NO3−)=62.0M(\text{NO}_3^-) = 62.0 g mol−1^{-1}).

For dilute aqueous solutions, 1 mg L−1^{-1} is 1 ppm, so the concentration is 25 ppm. In moles: 0.02562.0=4.0×10−4\dfrac{0.025}{62.0} = 4.0 \times 10^{-4} mol L−1^{-1}.

Command words

Word What it asks
Write (an equation) Balanced, with states when asked, and ionic where appropriate.
Describe Features, steps or observations, specifically.
Explain Cause and effect linked to a principle (collision theory, equilibrium, intermolecular forces, reactivity).
Calculate Working, units and sensible significant figures.
Compare Similarities and differences, side by side.
Evaluate A judgement about a procedure, process or claim, using evidence, including limitations.

Common mistakes

Where Chemistry marks go missing
  • Substituting moles instead of concentrations into a Kc expression.
  • Saying a catalyst shifts equilibrium. It speeds up both directions equally and does not change the yield at equilibrium.
  • Missing states, charges or electrons in equations and half-equations.
  • Confusing Rf values (TLC, a ratio of distances) with retention times (GC and HPLC, a time).
  • Writing the anode as negative in an electrolytic cell. In electrolysis the anode is positive.
  • Evaluations that say "human error" instead of naming a specific error and its effect on the result.

Six weeks to 4 November

  1. Week of 21 September: Topic 1: environmental chemistry, titrations, chromatography and spectroscopy.
  2. Week of 28 September: Topic 2: rates, equilibrium calculations and industrial compromise.
  3. Week of 5 October: Topic 3: organic families, reactions and biological molecules.
  4. Week of 12 October: Topic 4: energy, water, soil and materials. First past exam from the SACE website under 130-minute conditions.
  5. Week of 19 October: Second past exam, compared with the subject assessment advice; drill equations and calculations you missed.
  6. Week of 26 October to 3 November: Final past exam and a timed practice of evaluation questions.

Test yourself with the mixed exam-style quiz and the topics quiz.

Sources & how we know this

  • chemistry
  • sace
  • sace-chemistry
  • exam-strategy
  • equilibrium
  • volumetric-analysis
  • organic-chemistry
  • year-12
  • 2026
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