The required syllabus content for Unit 2, in order. Each card is one lesson-sized checkpoint.
Conceptual understanding: The mole makes it possible to correlate the number of particles with the mass that can be measured.
What is the meaning behind the term empirical formula?
Complete the following practical investigation to determine the water of crystallization of hydrated copper sulphate.
Lesson 4 of Unit 2.
Lesson 5 of Unit 2.
Watch the videos provided on how to graph data on excel
Lesson 8 of Unit 2.
Lesson 9 of Unit 2.
Lesson 10 of Unit 2.
Lesson 11 of Unit 2.
Conceptual understanding: Mole ratios in chemical equations can be used to calculate reacting ratios by mass and gas volume.
Each lesson card below mirrors the original teacher deck — syllabus refs, content, worked examples and practice questions in order.
The mole (mol) is the SI unit of amount of substance. One mole = exactly Avogadro's number of elementary entities — 6.022 × 10²³ — which is the same number of carbon atoms there are in exactly 12 g of ¹²C.
n = m / M · amount from mass and molar mass
n = N / NA · amount from particle count
N = n × NA · particle count from amount
Sum of relative atomic masses of all atoms in the formula unit. Mr(H₂O) = 2(1.01) + 16.00 = 18.02. Mr(Na₂SO₄·10H₂O) = 2(22.99) + 32.07 + 4(16.00) + 10(18.02) = 322.25.
Molar mass M in g mol⁻¹ is numerically equal to Mr.
The empirical formula is the simplest whole-number ratio of atoms in a compound. The molecular formula gives the actual count. They are related by a whole-number multiplier:
molecular formula = (empirical formula) × k where k = Mr(molecular) / Mr(empirical).
Burn a known mass in excess O₂. Measure the masses of CO₂ and H₂O produced. All the C ends up as CO₂; all the H ends up as H₂O. Any O in the original is found by subtracting (mass of C + mass of H) from the original sample mass.
Many ionic compounds crystallise with water molecules locked into the lattice. These are hydrated salts, written with a centred dot: CuSO₄·5H₂O is "copper(II) sulfate pentahydrate" — five waters per formula unit.
Heating drives off the water (the anhydrous salt remains). Measuring the mass before and after heating gives the ratio of moles of salt to moles of water, and hence the value of x in MX·xH₂O.
A balanced equation gives the ratios in which substances react. The five-step method works for every stoichiometry problem:
Golden rule: always convert to moles first.
A solution is a homogeneous mixture of a solute (dissolved substance) and a solvent (substance doing the dissolving — usually water in chemistry).
c = n / V mol dm⁻³ (molar concentration; square brackets [X] mean concentration of X)
ρ = m / V g dm⁻³ (mass concentration)
c = ρ / M (links the two via molar mass)
Unit conversion: 1 dm³ = 1000 cm³ = 1 L. Divide cm³ by 1000 to get dm³.
c1V1 = c2V2 · moles are conserved when only solvent is added.
A standard solution is one whose concentration is precisely known. They are needed for quantitative analysis — for titrations, calibration of spectrophotometers and determination of unknowns.
Dilute the stock solution by known factors (e.g. 1:2, 1:5, 1:10). Measure absorbance of each at a chosen λ in a spectrophotometer. Plot absorbance (y) vs concentration (x) — Beer-Lambert predicts a straight line through the origin (A = ε·c·l). Read unknown concentrations by matching their absorbance to the line.
A titration determines the concentration of one solution by reacting it with a measured volume of another of known concentration, until the reaction is complete.
For a balanced reaction aA + bB → products, at the endpoint:
n(A) / a = n(B) / b or equivalently cAVA / a = cBVB / b
The limiting reactant is the one fully consumed first — it sets the maximum amount of product. The excess reactant has some left over.
Method 1 (ratio): for each reactant, divide moles by its stoichiometric coefficient. The smallest answer wins.
Method 2 (test): pick one reactant, calculate how much of the other is needed. If the actual amount is less, that reactant is limiting.
Once the limiting reactant is identified, all further calculations (theoretical yield, excess remaining) start from its moles, not from the moles in the chemical equation.
Theoretical yield = maximum mass (or moles) of product calculated from the limiting reactant, assuming 100% conversion. Actual yield = mass actually obtained in the laboratory.
% yield = (actual / theoretical) × 100%
Reasons actual < theoretical: side reactions; equilibrium; product loss during transfer or purification; incomplete reaction; experimental error.
A different metric — looks at the percentage of atoms in the reactants that end up in the desired product:
AE = (Mr of desired product / Σ Mr of all reactants) × 100%
A high atom economy means little waste. A reaction can have 100% yield but only 30% atom economy if it produces lots of by-products. Atom economy is a key green-chemistry metric.
AE = (Mr of desired product / Σ Mr of all reactants) × 100%. Example: HCl + NaOH → NaCl + H₂O. Mr(NaCl) = 58.44. Total reactants = 36.46 + 40.00 = 76.46. AE = (58.44/76.46) × 100 = 76.4% — i.e. 23.6% of reactant mass is 'wasted' as H₂O.Avogadro's law: at the same temperature and pressure, equal volumes of any gases contain equal numbers of molecules. Equivalently, the volume per mole of any gas under the same conditions is the same — the molar volume.
At STP (273 K, 100 kPa): molar volume = 22.7 dm³ mol⁻¹.
For reactions involving only gases, you can work entirely in volume ratios — no need to convert to moles.
Boyle's law (constant T, n): pV = constant → halve V, double p.
Charles' law (constant p, n): V / T = constant → double T, double V.
Combined: p1V1/T1 = p2V2/T2.
pV = nRT
SI units: p in Pa (kPa × 1000), V in m³ (dm³ ÷ 1000, cm³ ÷ 10⁶), n in mol, T in K (°C + 273). R = 8.31 J K⁻¹ mol⁻¹.
Real gases deviate from ideal behaviour at low T (IMFs significant) and high p (particle volume non-negligible). Gases with strong IMFs (NH₃, H₂O) deviate more than non-polar gases (He, Ne).
If you can't define one of these in a sentence, that's where to revise next. Click any term for its definition.