频率按对应 unit 的 MS 数量计算:U1 条目 = hit / WCH11 MS,U2 条目 = hit / WCH12 MS。 Sources 使用本地原始 MS 文件名,最新来源排在前面;题号是文本抽取后的定位辅助,最终以原 PDF 为准。
Highest-Frequency First
| Frequency | Papers | Unit | Topic | Point | Full-mark wording | Sources |
|---|---|---|---|---|---|---|
| 96% | 22/23 | Unit 2 WCH12 | Group 7 Observation | Halogen displacement | The solution turns orange/brown because chlorine oxidises bromide ions to bromine; chlorine is a stronger oxidising agent than bromine.
| wch12-01-rms-20260305 Q5wch12-01a-rms-20260122 Q8wch12-01-rms-20260122 Q21wch12-01-rms-20250814 Q6+18 more |
| 96% | 22/23 | Unit 2 WCH12 | Halogenoalkanes Definition | Nucleophile | A species that donates a pair of electrons to form a covalent bond.
| wch12-01a-rms-20260305 Q21wch12-01-rms-20260305 Q21wch12-01a-rms-20260122 Q2wch12-01-rms-20260122 Q20+18 more |
| 96% | 22/23 | Unit 2 WCH12 | Kinetics and equilibria Explanation | Temperature and rate | Particles have higher kinetic energy, so they collide more frequently and a greater proportion of particles have energy equal to or greater than Ea; therefore there are more successful collisions per unit time.
| wch12-01a-rms-20260305 Q17wch12-01-rms-20260305 Q1wch12-01a-rms-20260122 Q1wch12-01-rms-20260122 Q6+18 more |
| 91% | 21/23 | Unit 1 WCH11 | Bonding and structure Explanation | Shape and lone pair repulsion | Lone pairs repel bonding pairs more strongly than bonding pairs repel each other, so the bonding pairs are pushed closer together and the bond angle decreases.
| wch11-01-rms-20260305 Q22wch11-01a-rms-20260122 Q21wch11-01-rms-20260122 Q14wch11-01-rms-20250814 Q21+17 more |
| 91% | 21/23 | Unit 2 WCH12 | Kinetics and equilibria Definition | Activation energy | The minimum energy that particles must have for a reaction to occur when they collide.
| wch12-01a-rms-20260305 Q24wch12-01-rms-20260305 Q1wch12-01a-rms-20260122 Q1wch12-01-rms-20260122+17 more |
| 87% | 20/23 | Unit 1 WCH11 | Alkenes Reaction | Electrophilic addition to alkenes | Curly arrow from the C=C π bond to the electrophile, bond-breaking arrow in the reagent, formation of a carbocation/intermediate, then attack by a nucleophile.
| wch11-01a-rms-20260305 Q24wch11-01-rms-20260305 Q23wch11-01a-rms-20260122 Q23wch11-01-rms-20250814 Q19+16 more |
| 87% | 20/23 | Unit 2 WCH12 | Group 7 Observation | Halide test with silver nitrate | Add dilute nitric acid then silver nitrate. Cl⁻ gives white AgCl soluble in dilute NH₃; Br⁻ gives cream AgBr soluble in concentrated NH₃; I⁻ gives yellow AgI insoluble in NH₃.
| wch12-01-rms-20260305 Q5wch12-01a-rms-20260122 Q4wch12-01-rms-20260122 Q20wch12-01-rms-20250814 Q13+16 more |
| 87% | 20/23 | Unit 2 WCH12 | Kinetics and equilibria Explanation | Le Chatelier pressure | The equilibrium shifts to the side with fewer moles of gas, reducing the pressure.
| wch12-01-rms-20260305 Q10wch12-01a-rms-20260122 Q12wch12-01-rms-20260122 Q3wch12-01-rms-20250814 Q11+16 more |
| 83% | 19/23 | Unit 2 WCH12 | Group 7 Trend | Halogen oxidising power | Down the group, atoms are larger and outer electrons are more shielded, so the nucleus attracts an incoming electron less strongly.
| wch12-01a-rms-20260305wch12-01-rms-20260305wch12-01a-rms-20260122 Q2wch12-01-rms-20250814+15 more |
| 78% | 18/23 | Unit 1 WCH11 | Alkanes Reaction | Free-radical substitution | Initiation: Cl₂ → 2Cl• under UV. Propagation: Cl• + CH₄ → HCl + CH₃•; CH₃• + Cl₂ → CH₃Cl + Cl•. Termination: two radicals combine.
| wch11-01a-rms-20260305 Q11wch11-01-rms-20260305 Q24wch11-01-rms-20260122 Q13wch11-01-rms-20250814 Q22+14 more |
| 78% | 18/23 | Unit 2 WCH12 | Kinetics and equilibria Explanation | Catalyst and rate | A catalyst provides an alternative reaction pathway with a lower activation energy, so a greater proportion of particles have E ≥ Ea.
| wch12-01a-rms-20260305 Q2wch12-01-rms-20260305 Q10wch12-01a-rms-20260122 Q21wch12-01-rms-20260122 Q22+14 more |
| 74% | 17/23 | Unit 1 WCH11 | Formulae, equations and amount Definition | Empirical formula | The simplest whole-number ratio of atoms of each element in a compound.
| wch11-01a-rms-20260305 Q1wch11-01-rms-20260305 Q8wch11-01-rms-20260122 Q3wch11-01-rms-20250814 Q12+13 more |
| 74% | 17/23 | Unit 2 WCH12 | Group 2 Trend | Thermal stability of Group 2 carbonates | Larger Group 2 cations have lower charge density and polarise the carbonate ion less, so the carbonate ion is less distorted and decomposes less readily.
| wch12-01a-rms-20260305 Q13wch12-01-rms-20260305 Q20wch12-01a-rms-20260122 Q7wch12-01-rms-20260122 Q13+13 more |
| 70% | 16/23 | Unit 1 WCH11 | Alkanes Definition | Free radical | A species with an unpaired electron.
| wch11-01a-rms-20260305 Q4wch11-01-rms-20260305 Q24wch11-01a-rms-20260122 Q17wch11-01-rms-20260122 Q13+12 more |
| 70% | 16/23 | Unit 1 WCH11 | Atomic structure Explanation | Successive ionisation evidence | A large jump shows the next electron is removed from an inner shell closer to the nucleus; the number of electrons removed before the jump equals the number of outer-shell electrons.
| wch11-01a-rms-20260305 Q16wch11-01-rms-20260305 Q1wch11-01-rms-20260122 Q14wch11-01-rms-20250814 Q23+12 more |
| 70% | 16/23 | Unit 2 WCH12 | Alcohols Reaction | Primary alcohol oxidation | Gentle oxidation and distillation gives an aldehyde; heating under reflux with excess acidified potassium dichromate(VI) gives a carboxylic acid.
| wch12-01-rms-20260305 Q14wch12-01a-rms-20260122 Q16wch12-01-rms-20250814 Q12wch12-01-rms-20250306+12 more |
| 65% | 15/23 | Unit 1 WCH11 | Alkenes Observation | Test for C=C | Shake with bromine water; orange/brown bromine water is decolourised.
| wch11-01-rms-20250306 Q16wch11-01-rms-20250116 Q15wch11-01-rms-20240815 Q19wch11-01-rms-20240307 Q15+11 more |
| 65% | 15/23 | Unit 2 WCH12 | Energetics Definition | Mean bond enthalpy | The enthalpy change required to break one mole of a specified covalent bond in gaseous molecules, averaged over a range of compounds.
| wch12-01a-rms-20260305 Q21wch12-01-rms-20260305 Q19wch12-01a-rms-20260122 Q15wch12-01-rms-20250306 Q19+11 more |
| 65% | 15/23 | Unit 2 WCH12 | Halogenoalkanes Reaction | Hydrolysis of halogenoalkanes | Warm/reflux with aqueous potassium hydroxide or aqueous sodium hydroxide; the reaction is nucleophilic substitution by OH⁻.
| wch12-01-rms-20260305wch12-01-rms-20250814wch12-01-rms-20250306wch12-01-rms-20240815+11 more |
| 61% | 14/23 | Unit 1 WCH11 | Alkanes Definition | Homolytic fission | Breaking a covalent bond so that each bonded atom receives one electron from the bond, forming radicals.
| wch11-01-rms-20260305 Q24wch11-01-rms-20260122 Q13wch11-01-rms-20250306 Q1wch11-01-rms-20240307 Q19+10 more |
| 61% | 14/23 | Unit 1 WCH11 | Bonding and structure Explanation | Sigma and pi bonds | A σ bond is formed by direct/head-on overlap of orbitals along the internuclear axis; a π bond is formed by sideways overlap of adjacent p orbitals above and below the σ bond.
| wch11-01a-rms-20260305 Q23wch11-01a-rms-20260122 Q23wch11-01-rms-20250814 Q21wch11-01-rms-20250116 Q20+10 more |
| 61% | 14/23 | Unit 2 WCH12 | Halogenoalkanes Reaction | Elimination from halogenoalkanes | Heat/reflux with ethanolic potassium hydroxide; H and X are eliminated to form an alkene.
| wch12-01-rms-20260305 Q21wch12-01a-rms-20260122 Q19wch12-01-rms-20250814 Q13wch12-01-rms-20250306 Q19+10 more |
| 57% | 13/23 | Unit 1 WCH11 | Alkenes Reaction | Addition polymerisation | Open the C=C double bond to a C-C single bond, keep the substituents on the same carbons, put brackets around the repeating unit and place n outside.
| wch11-01a-rms-20260305 Q22wch11-01-rms-20260305 Q23wch11-01a-rms-20260122 Q23wch11-01-rms-20260122+9 more |
| 57% | 13/23 | Unit 1 WCH11 | Atomic structure Definition | Isotopes | Atoms of the same element with the same number of protons but different numbers of neutrons.
| wch11-01a-rms-20260305 Q22wch11-01-rms-20260305 Q25wch11-01-rms-20260122 Q1wch11-01-rms-20250306 Q23+9 more |
| 57% | 13/23 | Unit 1 WCH11 | Bonding and structure Definition | Ionic bonding | The electrostatic attraction between oppositely charged ions.
| wch11-01-rms-20260305 Q21wch11-01a-rms-20260122 Q2wch11-01-rms-20250814wch11-01-rms-20250116 Q20+9 more |
| 57% | 13/23 | Unit 1 WCH11 | Bonding and structure Definition | Metallic bonding | The electrostatic attraction between positive metal ions and delocalised electrons.
| wch11-01a-rms-20260305 Q20wch11-01-rms-20260305 Q21wch11-01a-rms-20260122 Q8wch11-01-rms-20260122 Q15+9 more |
| 57% | 13/23 | Unit 2 WCH12 | Group 2 Trend | Group 2 sulfate solubility | Group 2 sulfates become less soluble down the group; BaSO₄ is very insoluble and forms a white precipitate.
| wch12-01a-rms-20260122 Q7wch12-01-rms-20260122 Q2wch12-01-rms-20250306 Q3wch12-01-rms-20250116 Q16+9 more |
| 57% | 13/23 | Unit 2 WCH12 | Organic analysis Observation | IR spectroscopy key absorptions | An O-H stretch in alcohols is broad around 3200-3600 cm⁻¹; a C=O absorption is strong around 1700 cm⁻¹.
| wch12-01-rms-20260305 Q1wch12-01-rms-20260122 Q14wch12-01-rms-20250814 Q2wch12-01-rms-20250306 Q18+9 more |
| 52% | 12/23 | Unit 2 WCH12 | Energetics Explanation | Heat loss consequence | The measured temperature change is smaller than the true value, so the calculated energy change is too small in magnitude.
| wch12-01a-rms-20260122 Q14wch12-01-rms-20250116 Q16wch12-01-rms-20240815 Q19wch12-01-rms-20240307 Q24+8 more |
| 48% | 11/23 | Unit 1 WCH11 | Bonding and structure Definition | Covalent bonding | The electrostatic attraction between the nuclei of two atoms and a shared pair of electrons.
| wch11-01-rms-20260305 Q21wch11-01-rms-20250814 Q23wch11-01-rms-20250306 Q10wch11-01-rms-20240307 Q9+7 more |
| 48% | 11/23 | Unit 1 WCH11 | Bonding and structure Definition | Dative covalent bond | A covalent bond in which both electrons in the shared pair are donated by the same atom.
| wch11-01a-rms-20260122 Q20wch11-01-rms-20250116 Q21wch11-01-rms-20240118 Q4wch11-01-rms-20230302 Q25+7 more |
| 48% | 11/23 | Unit 1 WCH11 | Formulae, equations and amount Definition | Relative atomic mass | The weighted mean mass of an atom of an element compared with one twelfth of the mass of an atom of carbon-12.
| wch11-01-rms-20260305 Q1wch11-01a-rms-20260122 Q5wch11-01-rms-20250306wch11-01-rms-20240815 Q16+7 more |
| 48% | 11/23 | Unit 2 WCH12 | Group 7 Definition | Disproportionation | A redox reaction in which the same element is both oxidised and reduced.
| wch12-01a-rms-20260305 Q10wch12-01-rms-20260122 Q21wch12-01-rms-20250306 Q10wch12-01-rms-20240118 Q7+7 more |
| 43% | 10/23 | Unit 1 WCH11 | Alkenes Reaction | Hydration of ethene | Steam with a phosphoric acid catalyst at high temperature and pressure.
| wch11-01a-rms-20260305 Q24wch11-01-rms-20260305 Q23wch11-01-rms-20240815 Q19wch11-01-rms-20230817 Q22+6 more |
| 43% | 10/23 | Unit 1 WCH11 | Bonding and structure Definition | Electronegativity | The ability of an atom to attract the bonding pair of electrons in a covalent bond.
| wch11-01-rms-20260305 Q22wch11-01-rms-20260122wch11-01-rms-20250306 Q10wch11-01-rms-20240118 Q20+6 more |
| 43% | 10/23 | Unit 2 WCH12 | Group 2 Trend | Group 2 hydroxide solubility | Group 2 hydroxides become more soluble down the group; barium hydroxide solution can be used to test for sulfate ions, giving white BaSO₄.
| wch12-01a-rms-20260122 Q5wch12-01-rms-20260122 Q2wch12-01r-rms-20240815 Q10wch12-01-rms-20240307 Q9+6 more |
| 39% | 9/23 | Unit 1 WCH11 | Atomic structure Definition | First ionisation energy | The energy required to remove one electron from each atom in one mole of gaseous atoms to form one mole of gaseous 1+ ions.
| wch11-01-rms-20260305 Q1wch11-01a-rms-20260122wch11-01-rms-20250814 Q21wch11-01-rms-20250306+5 more |
| 39% | 9/23 | Unit 2 WCH12 | Alcohols Reaction | Secondary and tertiary alcohol oxidation | A secondary alcohol is oxidised to a ketone; a tertiary alcohol is not oxidised under these conditions.
| wch12-01-rms-20260305 Q14wch12-01-rms-20250814 Q12wch12-01r-rms-20240815 Q17wch12-01-rms-20240815 Q0+5 more |
| 39% | 9/23 | Unit 2 WCH12 | Halogenoalkanes Explanation | Hydrolysis rate trend | The C-I bond has a lower bond enthalpy than C-Br and C-Cl, so it is weaker and breaks more easily.
| wch12-01a-rms-20260305 Q21wch12-01-rms-20250306 Q19wch12-01-rms-20250116 Q17wch12-01-rms-20240815 Q16+5 more |
| 35% | 8/23 | Unit 1 WCH11 | Intermolecular forces Explanation | London forces and boiling point | A larger molecule has more electrons and a larger surface area, so stronger London forces act between molecules; more energy is needed to overcome these intermolecular forces.
| wch11-01-rms-20250306 Q10wch11-01-rms-20230817 Q22wch11-01-rms-20230112WCH11_01_rms_20220303 Q22+4 more |
| 35% | 8/23 | Unit 1 WCH11 | Organic chemistry foundations Definition | E/Z stereoisomerism condition | There must be restricted rotation about the C=C double bond and each carbon of the C=C must have two different groups attached.
| wch11-01a-rms-20260305 Q23wch11-01a-rms-20260122wch11-01-rms-20260122 Q16wch11-01-rms-20250306 Q21+4 more |
| 30% | 7/23 | Unit 2 WCH12 | Kinetics and equilibria Definition | Le Chatelier's principle | When a system at equilibrium is disturbed, the equilibrium shifts to oppose the change.
| wch12-01-rms-20260305 Q12wch12-01a-rms-20260122 Q12wch12-01-rms-20250814 Q11wch12-01-rms-20250306 Q21+3 more |
| 26% | 6/23 | Unit 1 WCH11 | Organic chemistry foundations Definition | Structural isomers | Compounds with the same molecular formula but different structural formulae / different arrangement of atoms.
| wch11-01-rms-20260305 Q18wch11-01-rms-20260122 Q15wch11-01-rms-20250306 Q24wch11-01-rms-20240118 Q15+2 more |
| 26% | 6/23 | Unit 2 WCH12 | Alcohols Reaction | Dehydration of alcohols | Heat with concentrated sulfuric acid or pass vapour over hot aluminium oxide; water is eliminated to form an alkene.
| wch12-01-rms-20240118 Q8wch12-01-rms-20230817 Q18wch12-01-rms-20230112 Q21wch12-01-rms-20220818 Q0+2 more |
| 17% | 4/23 | Unit 2 WCH12 | Energetics Definition | Standard enthalpy change of combustion | The enthalpy change when one mole of a substance is completely burned in oxygen under standard conditions, with all substances in their standard states.
| wch12-01-rms-20260305 Q2wch12-01-rms-20240118 Q3wch12-01-rms-20230817wch12-01-rms-20220818 |
| 17% | 4/23 | Unit 2 WCH12 | Energetics Definition | Standard enthalpy change of formation | The enthalpy change when one mole of a compound is formed from its elements in their standard states under standard conditions.
| wch12-01-rms-20260305 Q2wch12-01-rms-20240118 Q1wch12-01-rms-20230112 Q2wch12-01-rms-20220818 Q1 |
| 13% | 3/23 | Unit 1 WCH11 | Alkanes Explanation | Alkanes are relatively unreactive | C-C and C-H bonds are strong / have high bond enthalpies, and the molecules are non-polar, so they are not readily attacked by electrophiles or nucleophiles.
| wch11-01-rms-20250306 Q21WCH11_01_msc_20210304 Q12WCH11_01_rms_20190815 Q3 |
| 9% | 2/23 | Unit 1 WCH11 | Organic chemistry foundations Definition | Functional group | The atom or group of atoms responsible for the characteristic chemical reactions of an organic compound.
| wch11-01-rms-20250306 Q21wch11-01-rms-20240307 |
| 4% | 1/23 | Unit 1 WCH11 | Alkenes Definition | Electrophile | A species that accepts a pair of electrons to form a covalent bond.
| WCH11_01_msc_20190307 Q13 |
| 4% | 1/23 | Unit 1 WCH11 | Organic chemistry foundations Definition | Homologous series | A series of organic compounds with the same functional group, similar chemical properties and successive members differing by CH₂.
| WCH11_01_msc_20210113 Q8 |
| 4% | 1/23 | Unit 2 WCH12 | Halogenoalkanes Definition | Heterolytic fission | Breaking a covalent bond so that both electrons from the bond go to one of the bonded atoms, forming ions.
| wch12-01-rms-20230817 Q19 |
| 4% | 1/23 | Unit 2 WCH12 | Kinetics and equilibria Definition | Dynamic equilibrium | In a closed system, the forward and reverse reactions occur at the same rate, so the concentrations of reactants and products remain constant.
| WCH12_01_rms_20220113 |
Appendix: specification / teacher-note points with no direct U1/U2 MS keyword hit
| Frequency | Papers | Unit | Topic | Point | Full-mark wording | Sources |
|---|---|---|---|---|---|---|
| 0% | 0/23 | Unit 1 WCH11 | Intermolecular forces Explanation | Branched alkane boiling point | Branching reduces surface contact between molecules, so London forces are weaker and less energy is needed to separate the molecules.
| specification / teacher notes |
| 0% | 0/23 | Unit 1 WCH11 | Intermolecular forces Explanation | Hydrogen bonding condition | Hydrogen bonding occurs when H is bonded to N, O or F and is attracted to a lone pair on N, O or F in another molecule.
| specification / teacher notes |
| 0% | 0/23 | Unit 2 WCH12 | Kinetics and equilibria Definition | Closed system | A system in which no substances enter or leave.
| specification / teacher notes |