International Baccalaureate · IB Diploma
Chemistry · HL
Papers, samples and curriculum documents for this course.
Handouts, exercise sheets and slides
Shared topic documents retain their source course and topic titles. Use your chosen board’s specification for coverage, tier and exam requirements.
Handouts · A-Level Chemistry (37)
- 1. Atomic structure
- 2. Atoms, molecules and stoichiometry
- 3. Chemical bonding
- 4. States of matter
- 5. Chemical energetics
- 6. Electrochemistry
- 7. Equilibria
- 8. Reaction kinetics
- 9. The Periodic Table: chemical periodicity
- 10. Group 2
- 11. Group 17
- 12. Nitrogen and sulfur
- 13. An introduction to AS Level organic chemistry
- 14. Hydrocarbons
- 15. Halogen compounds
- 16. Hydroxy compounds
- 17. Carbonyl compounds
- 18. Carboxylic acids and derivatives
- 19. Nitrogen compounds
- 20. Polymerisation
- 21. Organic synthesis
- 22. Analytical techniques
- 23. Chemical energetics
- 24. Electrochemistry
- 25. Equilibria
- 26. Reaction kinetics
- 27. Group 2
- 28. Chemistry of transition elements
- 29. An introduction to A Level organic chemistry
- 30. Hydrocarbons
- 31. Halogen compounds
- 32. Hydroxy compounds
- 33. Carboxylic acids and derivatives
- 34. Nitrogen compounds
- 35. Polymerisation
- 36. Organic synthesis
- 37. Analytical techniques
Exercise sheets · A-Level Chemistry (90)
- 1.1 Particles in the atom and atomic radius
- 1.2 Isotopes
- 1.3 Electrons, energy levels and atomic orbitals
- 1.4 Ionisation energy
- 2.1 Relative masses of atoms and molecules
- 2.2 The mole and the Avogadro constant
- 2.3 Formulas
- 2.4 Reacting masses and volumes (of solutions and gases)
- 3.1 Electronegativity and bonding
- 3.2 Ionic bonding
- 3.3 Metallic bonding
- 3.4 Covalent bonding and coordinate (dative covalent) bonding
- 3.5 Shapes of molecules
- 3.6 Intermolecular forces, electronegativity and bond properties
- 3.7 Dot-and-cross diagrams
- 4.1 The gaseous state: ideal and real gases and pV = nRT
- 4.2 Bonding and structure
- 5.1 Enthalpy change, ΔH
- 5.2 Hess’s law
- 6.1 Redox processes: electron transfer and changes in oxidation number (oxidation state)
- 7.1 Chemical equilibria: reversible reactions, dynamic equilibrium
- 7.2 Brønsted–Lowry theory of acids and bases
- 8.1 Rate of reaction
- 8.2 Effect of temperature on reaction rates and the concept of activation energy
- 8.3 Homogeneous and heterogeneous catalysts
- 9.1 Periodicity of physical properties of the elements in Period 3
- 9.2 Periodicity of chemical properties of the elements in Period 3
- 9.3 Chemical periodicity of other elements
- 10.1 Similarities and trends in the properties of the Group 2 metals, magnesium to barium, and their compounds
- 11.1 Physical properties of the Group 17 elements
- 11.2 The chemical properties of the halogen elements and the hydrogen halides
- 11.3 Some reactions of the halide ions
- 11.4 The reactions of chlorine
- 12.1 Nitrogen and sulfur
- 13.1 Formulas, functional groups and the naming of organic compounds
- 13.2 Characteristic organic reactions
- 13.3 Shapes of organic molecules; σ and π bonds
- 13.4 Isomerism: structural isomerism and stereoisomerism
- 14.1 Alkanes
- 14.2 Alkenes
- 15.1 Halogenoalkanes
- 16.1 Alcohols
- 17.1 Aldehydes and ketones
- 18.1 Carboxylic acids
- 18.2 Esters
- 19.1 Primary amines
- 19.2 Nitriles and hydroxynitriles
- 20.1 Addition polymerisation
- 21.1 Organic synthesis
- 22.1 Infrared spectroscopy
- 22.2 Mass spectrometry
- 23.1 Lattice energy and Born-Haber cycles
- 23.2 Enthalpies of solution and hydration
- 23.3 Entropy change, ΔS
- 23.4 Gibbs free energy change, ΔG
- 24.1 Electrolysis
- 24.2 Standard electrode potentials E⦵, standard cell potentials E⦵cell and the Nernst equation
- 25.1 Acids and bases
- 25.2 Partition coefficients
- 26.1 Simple rate equations, orders of reaction and rate constants
- 26.2 Homogeneous and heterogeneous catalysts
- 27.1 Similarities and trends in the properties of the Group 2 metals, magnesium to barium, and their compounds
- 28.1 General physical and chemical properties of the first row of transition elements, titanium to copper
- 28.2 General characteristic chemical properties of the first set of transition elements, titanium to copper
- 28.3 Colour of complexes
- 28.4 Stereoisomerism in transition element complexes
- 28.5 Stability constants, Kstab
- 29.1 Formulas, functional groups and the naming of organic compounds
- 29.2 Characteristic organic reactions
- 29.3 Shapes of aromatic organic molecules; σ and π bonds
- 29.4 Isomerism: optical
- 30.1 Arenes
- 31.1 Halogen compounds
- 32.1 Alcohols
- 32.2 Phenol
- 33.1 Carboxylic acids
- 33.2 Esters
- 33.3 Acyl chlorides
- 34.1 Primary and secondary amines
- 34.2 Phenylamine and azo compounds
- 34.3 Amides
- 34.4 Amino acids
- 35.1 Condensation polymerisation
- 35.2 Predicting the type of polymerisation
- 35.3 Degradable polymers
- 36.1 Organic synthesis
- 37.1 Thin-layer chromatography
- 37.2 Gas/liquid chromatography
- 37.3 Carbon-13 NMR spectroscopy
- 37.4 Proton (1H) NMR spectroscopy
Presentation slides · A-Level Chemistry (37)
- 1. Atomic structure
- 2. Atoms, molecules and stoichiometry
- 3. Chemical bonding
- 4. States of matter
- 5. Chemical energetics
- 6. Electrochemistry
- 7. Equilibria
- 8. Reaction kinetics
- 9. The Periodic Table: chemical periodicity
- 10. Group 2
- 11. Group 17
- 12. Nitrogen and sulfur
- 13. An introduction to AS Level organic chemistry
- 14. Hydrocarbons
- 15. Halogen compounds
- 16. Hydroxy compounds
- 17. Carbonyl compounds
- 18. Carboxylic acids and derivatives
- 19. Nitrogen compounds
- 20. Polymerisation
- 21. Organic synthesis
- 22. Analytical techniques
- 23. Chemical energetics
- 24. Electrochemistry
- 25. Equilibria
- 26. Reaction kinetics
- 27. Group 2
- 28. Chemistry of transition elements
- 29. An introduction to A Level organic chemistry
- 30. Hydrocarbons
- 31. Halogen compounds
- 32. Hydroxy compounds
- 33. Carboxylic acids and derivatives
- 34. Nitrogen compounds
- 35. Polymerisation
- 36. Organic synthesis
- 37. Analytical techniques
Course units and learning goals
These lessons teach selected course objectives. Check the remaining coverage gaps; the material is not a complete preparation programme.
Structure 1.1 · Introduction to the particulate nature of matter
- Temperature on the kelvin scale.
- At fixed amount and volume, pressure is proportional to kelvin temperature. At fixed temperature and amount, pressure is inversely proportional to volume. State which quantities are fixed before choosing a relationship.
- Use approved apparatus with a temperature range and pressure limit set by the teacher. Allow thermal equilibrium and record pressure against kelvin temperature. Never heat an improvised sealed vessel.
- absolute temperature
- Temperature on the kelvin scale
- ideal gas
- A gas model with specified simplifying assumptions
Structure 1.2 · The nuclear atom
- Attraction between oppositely charged ions.
- To explain a bulk property, name the structure, particles, forces and mobile charge carriers. Simple molecular substances can have strong covalent bonds inside molecules but weak attractions between molecules.
- Compare substances using evidence such as melting point, conductivity when solid and molten, and solubility. One property rarely proves a structure; use a pattern of evidence.
- ionic bond
- Attraction between oppositely charged ions
- delocalized electron
- An electron not confined to one atom or bond
Structure 1.3 · Electron configurations
- Attraction between oppositely charged ions.
- To explain a bulk property, name the structure, particles, forces and mobile charge carriers. Simple molecular substances can have strong covalent bonds inside molecules but weak attractions between molecules.
- Compare substances using evidence such as melting point, conductivity when solid and molten, and solubility. One property rarely proves a structure; use a pattern of evidence.
- ionic bond
- Attraction between oppositely charged ions
- delocalized electron
- An electron not confined to one atom or bond
Structure 1.4 · Counting particles by mass: the mole
- The SI unit of amount of substance.
- Calculate the amount available for each reactant and divide by its coefficient. The smaller ratio limits the reaction. Use that reactant to calculate the maximum product before comparing actual yield.
- Write the balanced equation first, include units in molar masses, then convert each given mass or solution volume into amount. Convert cubic centimetres to cubic decimetres before using concentration in moles per cubic decimetre.
- mole
- The SI unit of amount of substance
- limiting reagent
- The reactant that limits the possible product amount
Structure 1.5 · Ideal gases
- Temperature on the kelvin scale.
- At fixed amount and volume, pressure is proportional to kelvin temperature. At fixed temperature and amount, pressure is inversely proportional to volume. State which quantities are fixed before choosing a relationship.
- Use approved apparatus with a temperature range and pressure limit set by the teacher. Allow thermal equilibrium and record pressure against kelvin temperature. Never heat an improvised sealed vessel.
- absolute temperature
- Temperature on the kelvin scale
- ideal gas
- A gas model with specified simplifying assumptions
Structure 2.1 · The ionic model
- Attraction between oppositely charged ions.
- To explain a bulk property, name the structure, particles, forces and mobile charge carriers. Simple molecular substances can have strong covalent bonds inside molecules but weak attractions between molecules.
- Compare substances using evidence such as melting point, conductivity when solid and molten, and solubility. One property rarely proves a structure; use a pattern of evidence.
- ionic bond
- Attraction between oppositely charged ions
- delocalized electron
- An electron not confined to one atom or bond
Structure 2.2 · The covalent model
- Attraction between oppositely charged ions.
- To explain a bulk property, name the structure, particles, forces and mobile charge carriers. Simple molecular substances can have strong covalent bonds inside molecules but weak attractions between molecules.
- Compare substances using evidence such as melting point, conductivity when solid and molten, and solubility. One property rarely proves a structure; use a pattern of evidence.
- ionic bond
- Attraction between oppositely charged ions
- delocalized electron
- An electron not confined to one atom or bond
Structure 2.3 · The metallic model
- Attraction between oppositely charged ions.
- To explain a bulk property, name the structure, particles, forces and mobile charge carriers. Simple molecular substances can have strong covalent bonds inside molecules but weak attractions between molecules.
- Compare substances using evidence such as melting point, conductivity when solid and molten, and solubility. One property rarely proves a structure; use a pattern of evidence.
- ionic bond
- Attraction between oppositely charged ions
- delocalized electron
- An electron not confined to one atom or bond
Structure 2.4 · From models to materials
- Attraction between oppositely charged ions.
- To explain a bulk property, name the structure, particles, forces and mobile charge carriers. Simple molecular substances can have strong covalent bonds inside molecules but weak attractions between molecules.
- Compare substances using evidence such as melting point, conductivity when solid and molten, and solubility. One property rarely proves a structure; use a pattern of evidence.
- ionic bond
- Attraction between oppositely charged ions
- delocalized electron
- An electron not confined to one atom or bond
Structure 3.1 · The periodic table: classification of elements
- Attraction between oppositely charged ions.
- To explain a bulk property, name the structure, particles, forces and mobile charge carriers. Simple molecular substances can have strong covalent bonds inside molecules but weak attractions between molecules.
- Compare substances using evidence such as melting point, conductivity when solid and molten, and solubility. One property rarely proves a structure; use a pattern of evidence.
- ionic bond
- Attraction between oppositely charged ions
- delocalized electron
- An electron not confined to one atom or bond
Structure 3.2 · Functional groups: classification of organic compounds
- An atom group determining characteristic reactions.
- Distinguish addition, substitution, oxidation and polymerization by tracing bonds before and after reaction. Conditions and reagents belong to the reaction arrow; they are not interchangeable labels.
- Draw displayed or structural formulae with the correct number of bonds at each carbon. Use a carbon count to check a proposed synthesis. At advanced level, track reagents and conditions through multistep routes.
- functional group
- An atom group determining characteristic reactions
- isomer
- A compound sharing a formula but differing in structure
Reactivity 1.1 · Measuring enthalpy change
- Transferring energy to the surroundings.
- Use energy transferred = mass × specific heat capacity × temperature change. Convert joules to kilojoules before dividing by reaction amount. An exothermic molar enthalpy change has a negative sign.
- Use insulation and a lid, measure starting temperatures consistently, stir, and record a temperature-time series. Estimate the reaction temperature from an appropriate extrapolation rather than ignoring cooling during measurement.
- exothermic
- Transferring energy to the surroundings
- enthalpy change
- Heat change at constant pressure for a stated process
Reactivity 1.2 · Energy cycles in reactions
- Transferring energy to the surroundings.
- Use energy transferred = mass × specific heat capacity × temperature change. Convert joules to kilojoules before dividing by reaction amount. An exothermic molar enthalpy change has a negative sign.
- Use insulation and a lid, measure starting temperatures consistently, stir, and record a temperature-time series. Estimate the reaction temperature from an appropriate extrapolation rather than ignoring cooling during measurement.
- exothermic
- Transferring energy to the surroundings
- enthalpy change
- Heat change at constant pressure for a stated process
Reactivity 1.3 · Energy from fuels
- Assessment across production, use and disposal.
- Define the functional unit before comparing products. The same delivered service, such as carrying one litre of water a hundred times, is fairer than comparing one object with another regardless of lifetime.
- List system boundaries, energy sources and assumptions. Compare water demand, emissions and waste separately before making a judgement. Explain whose priorities affect the decision and where the data are uncertain.
- life-cycle assessment
- Assessment across production, use and disposal
- functional unit
- The common service used for a fair comparison
Reactivity 1.4 · Entropy and spontaneity
- A state property related to energy dispersal and accessible arrangements.
- Use ΔG = ΔH - TΔS with consistent energy units. A negative Gibbs energy change indicates thermodynamic favourability for the stated conditions, not a fast rate. An activation barrier can make a favourable process slow.
- State whether values are standard-state quantities and record temperature in kelvin. Convert entropy from joules per kelvin per mole into kilojoules per kelvin per mole when enthalpy is in kilojoules per mole.
- entropy
- A state property related to energy dispersal and accessible arrangements
- Gibbs energy
- A thermodynamic quantity combining enthalpy and entropy contributions
Reactivity 2.1 · How much? The amount of chemical change
- The SI unit of amount of substance.
- Calculate the amount available for each reactant and divide by its coefficient. The smaller ratio limits the reaction. Use that reactant to calculate the maximum product before comparing actual yield.
- Write the balanced equation first, include units in molar masses, then convert each given mass or solution volume into amount. Convert cubic centimetres to cubic decimetres before using concentration in moles per cubic decimetre.
- The volume delivered between two burette readings.
- Calculate the known amount first, apply the stoichiometric ratio, then divide by the unknown solution volume in cubic decimetres. Use concordant titres as required by the school method and report the accepted values.
- Rinse the burette with its solution and the pipette with the solution it transfers. Rinse the flask with distilled water. Add titrant slowly near the endpoint, swirl, and read the meniscus at eye level. Use a white tile and appropriate eye protection.
- mole
- The SI unit of amount of substance
- limiting reagent
- The reactant that limits the possible product amount
- titre
- The volume delivered between two burette readings
- equivalence point
- The point of stoichiometric reaction completion
Reactivity 2.2 · How fast? The rate of chemical change
- The energy barrier for a reaction pathway.
- A product-time graph has a steeper gradient where rate is larger. A tangent estimates instantaneous rate; a secant gives average rate over an interval. The final plateau reflects the total collected product under the stated conditions.
- For gas production, check apparatus for leaks, start timing consistently and record volume at regular intervals. Keep concentration, reactant amount and surface area controlled when changing temperature.
- activation energy
- The energy barrier for a reaction pathway
- rate
- Change in a measured quantity per unit time
Reactivity 2.3 · How far? The extent of chemical change
- A state with equal forward and reverse reaction rates.
- A concentration or pressure change disturbs the balance. The system responds toward a new equilibrium. Temperature changes can also change the equilibrium constant; a catalyst changes how quickly equilibrium is reached.
- State the balanced equation and whether the forward reaction is exothermic before predicting a temperature effect. Count gas coefficients when considering pressure; pressure has no composition effect when gaseous amounts are equal on both sides.
- equilibrium
- A state with equal forward and reverse reaction rates
- reversible reaction
- A reaction that can proceed in both directions
Reactivity 3.1 · Proton transfer reactions
- The volume delivered between two burette readings.
- Calculate the known amount first, apply the stoichiometric ratio, then divide by the unknown solution volume in cubic decimetres. Use concordant titres as required by the school method and report the accepted values.
- Rinse the burette with its solution and the pipette with the solution it transfers. Rinse the flask with distilled water. Add titrant slowly near the endpoint, swirl, and read the meniscus at eye level. Use a white tile and appropriate eye protection.
- titre
- The volume delivered between two burette readings
- equivalence point
- The point of stoichiometric reaction completion
Reactivity 3.2 · Electron transfer reactions
- Loss of electrons.
- Predict products using the specified electrolyte and electrode material. In an aqueous solution, hydrogen or oxygen may form because water-related species compete. Molten salts contain only the ions of the salt.
- Use a low-voltage direct-current supply, approved electrodes, and the school risk assessment. Collect gases only by an approved method. Keep chlorine demonstrations teacher-controlled; do not ask students to generate hazardous gases independently.
- oxidation
- Loss of electrons
- reduction
- Gain of electrons
Reactivity 3.3 · Electron sharing reactions
- An atom group determining characteristic reactions.
- Distinguish addition, substitution, oxidation and polymerization by tracing bonds before and after reaction. Conditions and reagents belong to the reaction arrow; they are not interchangeable labels.
- Draw displayed or structural formulae with the correct number of bonds at each carbon. Use a carbon count to check a proposed synthesis. At advanced level, track reagents and conditions through multistep routes.
- functional group
- An atom group determining characteristic reactions
- isomer
- A compound sharing a formula but differing in structure
Reactivity 3.4 · Electron-pair sharing reactions
- An atom group determining characteristic reactions.
- Distinguish addition, substitution, oxidation and polymerization by tracing bonds before and after reaction. Conditions and reagents belong to the reaction arrow; they are not interchangeable labels.
- Draw displayed or structural formulae with the correct number of bonds at each carbon. Use a carbon count to check a proposed synthesis. At advanced level, track reagents and conditions through multistep routes.
- functional group
- An atom group determining characteristic reactions
- isomer
- A compound sharing a formula but differing in structure
Practical · Experimental programme
- A quantified limitation on a measured result.
- For a product or quotient, adding fractional uncertainties is a common maximum-uncertainty approximation. For a difference, add absolute uncertainties. A nonzero intercept can reveal an offset or an incomplete model.
- Show units on axes and choose a sensible scale. Plot uncertainty bars where justified, draw a best-fit line rather than joining every point, and estimate steepest and shallowest plausible gradients when the course method calls for them.
- uncertainty
- A quantified limitation on a measured result
- systematic error
- A consistent measurement bias
Preparing for this qualification
- Structure and reactivity replace the old topic/option model. Entropy and spontaneity is AHL; all other topics still require exact SL/AHL statement separation from the guide.
- Paper 1A MCQ + 1B experimental/data work, Paper 2 short/extended responses; SL 1.5/1.5 h, HL 2/2.5 h; weights 36%/44%. Scientific investigation 20%, 3,000 words.
- Practical work 40 h plus collaborative sciences project 10 h and investigation 10 h; use the current chemistry data booklet.
Teaching coverage still needed
- Full 2025 SL/AHL understanding and guidance statements are not established by the brief. Focus cases do not cover complete bonding, acid-base, mechanism or spectroscopy objectives.
- Full experimental-technique objectives and current data booklet need acquisition.
Specifications and sample documents
- Chemistry — Subject brief · 2025 ↗
First assessment: 2025
- IB Chemistry guide first assessment 2025 ↗
Course materials
Course preparation
Documents are available. Board-specific notes, assessments and interactive past-paper practice are not yet available for every course.
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