Pearson Edexcel · A Level · 9CH0
Pearson Edexcel A Level Chemistry (9CH0)
Topic-by-topic keywords, key terms and definitions for precise exam language—separate from our revision checklists (topic coverage) and formula sheets (equations).
Examiner-style keywords and definitions organised by syllabus topic. Terms are tagged Essential (start here), Core (typical exam standard), and Advanced for harder distinctions — tick each row when you can recall it. Your progress is saved in this browser for this list.
Pearson Edexcel A Level Chemistry (9CH0)
Pearson Edexcel A Level Chemistry (9CH0)
Pearson Edexcel Chemistry (9CH0) topics 1–19 span atomic structure and the periodic table, bonding and structure, redox, inorganic chemistry, formulae/equations/amounts, organic chemistry, modern analytical techniques, energetics, kinetics, equilibria and transition metals — assessed across Papers 1–3 with Core Practicals.
Mark schemes: Pearson Edexcel rewards linked reasoning, precise IUPAC names, state symbols in equations and correct units (kJ mol⁻¹, mol dm⁻³). ΔH signs must match the exothermic/endothermic context; equilibrium expressions raise concentrations or partial pressures to stoichiometric powers. Mechanisms require curly arrows from a bond or lone pair to an electrophilic centre, with δ+/δ− shown where relevant.
Active recall: 0 / 20 terms ticked
| Recalled | Topic | Level | Keyword | Definition |
|---|---|---|---|---|
| Atoms, moles & gases | Essential | Mole | Amount of substance containing 6.02 × 10²³ specified entities (Avogadro's constant). | |
| Atoms, moles & gases | Core | Mass–mole relation | n = m/M, where m is mass in g and M is molar mass in g mol⁻¹. | |
| Atoms, moles & gases | Core | Concentration | n = cV, where c is in mol dm⁻³ and V in dm³. | |
| Atoms, moles & gases | Core | Ideal gas equation | pV = nRT with R = 8.31 J K⁻¹ mol⁻¹ and SI units throughout. | |
| Atoms, moles & gases | Advanced | Empirical vs molecular formula | Empirical is the simplest whole-number ratio; molecular is the actual number of atoms per molecule. | |
| Energetics & kinetics | Core | Hess's law | ΔH = Σ ΔHf(products) − Σ ΔHf(reactants); enthalpy change is route-independent. | |
| Energetics & kinetics | Core | Born–Haber cycle | Thermochemical cycle used to determine lattice enthalpy from measurable enthalpy changes. | |
| Energetics & kinetics | Core | Gibbs free energy | ΔG = ΔH − TΔS; reaction is feasible when ΔG < 0 at the stated temperature. | |
| Energetics & kinetics | Core | Rate equation | Experimentally determined: rate = k[A]^m[B]^n with overall order m + n. | |
| Energetics & kinetics | Advanced | Arrhenius equation | k = A e^(−Ea/RT); plot of ln k against 1/T has gradient −Ea/R. | |
| Equilibria & redox | Core | Equilibrium constants Kc and Kp | Kc uses equilibrium concentrations; Kp uses partial pressures of gases. | |
| Equilibria & redox | Core | pH and Ka | pH = −log[H⁺]; Ka = [H⁺][A⁻]/[HA] for a weak acid dissociation. | |
| Equilibria & redox | Core | Henderson–Hasselbalch | Buffer pH = pKa + log([A⁻]/[HA]); resists pH change on small additions of acid or base. | |
| Equilibria & redox | Core | Standard electrode potential | E° measured versus the standard hydrogen electrode under standard conditions. | |
| Equilibria & redox | Advanced | E°cell | E°cell = E°(cathode) − E°(anode); positive value indicates a feasible redox reaction under standard conditions. | |
| Organic chemistry & analysis | Core | Nucleophilic substitution | Nucleophile replaces a leaving group at a saturated carbon via SN1 or SN2. | |
| Organic chemistry & analysis | Core | Electrophilic addition | Alkenes attacked by an electrophile across the C=C double bond. | |
| Organic chemistry & analysis | Core | ¹H and ¹³C NMR | Spectra showing chemical environments of hydrogen and carbon atoms via chemical shift. | |
| Organic chemistry & analysis | Core | Infrared spectroscopy | Identifies functional groups from characteristic absorption wavenumbers. | |
| Organic chemistry & analysis | Advanced | Mass spectrometry | Molecular ion peak gives Mr; fragmentation pattern aids structure elucidation. |
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