Diploma del Bachillerato Internacional · IB Diploma
Chemistry · SL
Papers, samples and curriculum documents for this course. · Papeles, muestras y documentos curriculares para este curso.
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 · Material de apoyo · A-Level Chemistry · A-Level Química (37)
- 1. Atomic structure · 1. Estructura atómica
- 2. Atoms, molecules and stoichiometry · 2. Átomos, moléculas y estequiometría
- 3. Chemical bonding · 3. Enlace químico
- 4. States of matter · 4. Estados de la materia
- 5. Chemical energetics · 5. Energetica química
- 6. Electrochemistry · 6. Electroquímica
- 7. Equilibria · 7. Equilibrios
- 8. Reaction kinetics · 8. Cinética de reacción
- 9. The Periodic Table: chemical periodicity · 9. La Tabla Periódica: periodicidad química
- 10. Group 2 · 10. Grupo 2
- 11. Group 17 · 11. Grupo 17
- 12. Nitrogen and sulfur · 12. Nitrógeno y azufre
- 13. An introduction to AS Level organic chemistry · 13. Una introducción a la química orgánica AS Level
- 14. Hydrocarbons · 14. Hidrocarburos
- 15. Halogen compounds · 15. Compuestos halogenados
- 16. Hydroxy compounds · 16. Compuestos hidroxilados
- 17. Carbonyl compounds · 17. Compuestos carbonilo
- 18. Carboxylic acids and derivatives · 18. Ácidos carboxílicos y derivados
- 19. Nitrogen compounds · 19. Compuestos de nitrógeno
- 20. Polymerisation · 20. Polimerización
- 21. Organic synthesis · 21. Síntesis orgánica
- 22. Analytical techniques · 22. Técnicas analíticas
- 23. Chemical energetics · 23. Energetica química
- 24. Electrochemistry · 24. Electroquímica
- 25. Equilibria · 25. Equilibrios
- 26. Reaction kinetics · 26. Cinética de reacción
- 27. Group 2 · 27. Grupo 2
- 28. Chemistry of transition elements · 28. Química de elementos de transición
- 29. An introduction to A Level organic chemistry · 29. Una introducción a la química orgánica A Level
- 30. Hydrocarbons · 30. Hidrocarburos
- 31. Halogen compounds · 31. Compuestos halogenados
- 32. Hydroxy compounds · 32. Compuestos hidroxilados
- 33. Carboxylic acids and derivatives · 33. Ácidos carboxílicos y derivados
- 34. Nitrogen compounds · 34. Compuestos de nitrógeno
- 35. Polymerisation · 35. Polimerización
- 36. Organic synthesis · 36. Síntesis orgánica
- 37. Analytical techniques · 37. Técnicas analíticas
Exercise sheets · Hojas de ejercicios · A-Level Chemistry · A-Level Química (90)
- 1.1 Particles in the atom and atomic radius · 1.1 Parteículas en el átomo y radio atómico
- 1.2 Isotopes · 1.2 Isótopos
- 1.3 Electrons, energy levels and atomic orbitals · 1.3 Electrones, niveles de energía y orbitales atómicos
- 1.4 Ionisation energy · 1.4 Energía de ionización
- 2.1 Relative masses of atoms and molecules · 2.1 Masas relativas de átomos y moléculas
- 2.2 The mole and the Avogadro constant · 2.2 El mol y la constante de Avogadro
- 2.3 Formulas · 2.3 Fórmulas
- 2.4 Reacting masses and volumes (of solutions and gases) · 2.4 Masas y volúmenes de reacción (soluciones y gases)
- 3.1 Electronegativity and bonding · 3.1 Electronegatividad y enlace
- 3.2 Ionic bonding · 3.2 Enlace iónico
- 3.3 Metallic bonding · 3.3 Enlace metálico
- 3.4 Covalent bonding and coordinate (dative covalent) bonding · 3.4 Enlace covalente y enlace dativo (covalente coordenado)
- 3.5 Shapes of molecules · 3.5 Formas de las moléculas
- 3.6 Intermolecular forces, electronegativity and bond properties · 3.6 Fuerzas intermoleculares, electronegatividad y propiedades del enlace
- 3.7 Dot-and-cross diagrams · 3.7 Diagramas de puntos y cruces
- 4.1 The gaseous state: ideal and real gases and pV = nRT · 4.1 Estado gaseoso: gases ideales y reales y pV = nRT
- 4.2 Bonding and structure · 4.2 Enlace y estructura
- 5.1 Enthalpy change, ΔH · 5.1 Cambio de entalpía, ΔH
- 5.2 Hess’s law · 5.2 Ley de Hess
- 6.1 Redox processes: electron transfer and changes in oxidation number (oxidation state) · 6.1 Procesos redox: transferencia de electrones y cambios en el número de oxidación (estado de oxidación)
- 7.1 Chemical equilibria: reversible reactions, dynamic equilibrium · 7.1 Equilibrio químico: reacciones reversibles, equilibrio dinámico
- 7.2 Brønsted–Lowry theory of acids and bases · 7.2 Teoría de Brønsted–Lowry de ácidos y bases
- 8.1 Rate of reaction · 8.1 Velocidad de reacción
- 8.2 Effect of temperature on reaction rates and the concept of activation energy · 8.2 Efecto de la temperatura sobre las velocidades de reacción y el concepto de energía de activación
- 8.3 Homogeneous and heterogeneous catalysts · 8.3 Catálisis homogénea y heterogénea
- 9.1 Periodicity of physical properties of the elements in Period 3 · 9.1 Periodicidad de las propiedades físicas de los elementos del Periodo 3
- 9.2 Periodicity of chemical properties of the elements in Period 3 · 9.2 Periodicidad de las propiedades químicas de los elementos del Periodo 3
- 9.3 Chemical periodicity of other elements · 9.3 Periodicidad química de otros elementos
- 10.1 Similarities and trends in the properties of the Group 2 metals, magnesium to barium, and their compounds · 10.1 Similitudes y tendencias en las propiedades de los metales del Grupo 2, magnesio a bario, y sus compuestos
- 11.1 Physical properties of the Group 17 elements · 11.1 Propiedades físicas de los elementos del Grupo 17
- 11.2 The chemical properties of the halogen elements and the hydrogen halides · 11.2 Propiedades químicas de los halógenos y los haluros de hidrógeno
- 11.3 Some reactions of the halide ions · 11.3 Algunas reacciones de los iones haluro
- 11.4 The reactions of chlorine · 11.4 Reacciones del cloro
- 12.1 Nitrogen and sulfur · 12.1 Nitrógeno y azufre
- 13.1 Formulas, functional groups and the naming of organic compounds · 13.1 Fórmulas, grupos funcionales y nomenclatura de compuestos orgánicos
- 13.2 Characteristic organic reactions · 13.2 Reacciones orgánicas características
- 13.3 Shapes of organic molecules; σ and π bonds · 13.3 Geometrías de moléculas orgánicas; enlaces σ y π
- 13.4 Isomerism: structural isomerism and stereoisomerism · 13.4 Isomerismo: isomería estructural y estereoisomería
- 14.1 Alkanes · 14.1 Alcanos
- 14.2 Alkenes · 14.2 Alquenos
- 15.1 Halogenoalkanes · 15.1 Halogenoalcanos
- 16.1 Alcohols · 16.1 Alcoholes
- 17.1 Aldehydes and ketones · 17.1 Aldehídos y cetonas
- 18.1 Carboxylic acids · 18.1 Ácidos carboxílicos
- 18.2 Esters · 18.2 Ésteres
- 19.1 Primary amines · 19.1 Aminas primarias
- 19.2 Nitriles and hydroxynitriles · 19.2 Nitrilos y hidroxinitrilos
- 20.1 Addition polymerisation · 20.1 Polimerización por adición
- 21.1 Organic synthesis · 21.1 Síntesis orgánica
- 22.1 Infrared spectroscopy · 22.1 Espectroscopía infrarroja
- 22.2 Mass spectrometry · 22.2 Espectrometría de masas
- 23.1 Lattice energy and Born-Haber cycles · 23.1 Energía reticular y ciclos de Born-Haber
- 23.2 Enthalpies of solution and hydration · 23.2 Entalpías de disolución e hidratación
- 23.3 Entropy change, ΔS · 23.3 Cambio de entropía, ΔS
- 23.4 Gibbs free energy change, ΔG · 23.4 Cambio de energía libre de Gibbs, ΔG
- 24.1 Electrolysis · 24.1 Electrólisis
- 24.2 Standard electrode potentials E⦵, standard cell potentials E⦵cell and the Nernst equation · 24.2 Potenciales estándar de electrodo E⦵, potenciales estándar de celda E⦵cell y ecuación de Nernst
- 25.1 Acids and bases · 25.1 Ácidos y bases
- 25.2 Partition coefficients · 25.2 Coeficientes de partición
- 26.1 Simple rate equations, orders of reaction and rate constants · 26.1 Ecuaciones de velocidad simples, órdenes de reacción y constantes de velocidad
- 26.2 Homogeneous and heterogeneous catalysts · 26.2 Catálisis homogénea y heterogénea
- 27.1 Similarities and trends in the properties of the Group 2 metals, magnesium to barium, and their compounds · 27.1 Similitudes y tendencias en las propiedades de los metales del Grupo 2, magnesio a bario, y sus compuestos
- 28.1 General physical and chemical properties of the first row of transition elements, titanium to copper · 28.1 Propiedades físicas y químicas generales de la primera fila de elementos de transición, titanio a cobre
- 28.2 General characteristic chemical properties of the first set of transition elements, titanium to copper · 28.2 Propiedades químicas características generales del primer conjunto de elementos de transición, titanio a cobre
- 28.3 Colour of complexes · 28.3 Color de los complejos
- 28.4 Stereoisomerism in transition element complexes · 28.4 Estereoisomería en complejos de elementos de transición
- 28.5 Stability constants, Kstab · 28.5 Constantes de estabilidad, Kstab
- 29.1 Formulas, functional groups and the naming of organic compounds · 29.1 Fórmulas, grupos funcionales y nomenclatura de compuestos orgánicos
- 29.2 Characteristic organic reactions · 29.2 Reacciones orgánicas características
- 29.3 Shapes of aromatic organic molecules; σ and π bonds · 29.3 Geometrías de moléculas orgánicas aromáticas; enlaces σ y π
- 29.4 Isomerism: optical · 29.4 Isomerismo: óptico
- 30.1 Arenes · 30.1 Arenas
- 31.1 Halogen compounds · 31.1 Compuestos halogenados
- 32.1 Alcohols · 32.1 Alcoholes
- 32.2 Phenol · 32.2 Fenol
- 33.1 Carboxylic acids · 33.1 Ácidos carboxílicos
- 33.2 Esters · 33.2 Ésteres
- 33.3 Acyl chlorides · 33.3 Cloruros de acilo
- 34.1 Primary and secondary amines · 34.1 Aminas primarias y secundarias
- 34.2 Phenylamine and azo compounds · 34.2 Fenilamina y compuestos azo
- 34.3 Amides · 34.3 Amidas
- 34.4 Amino acids · 34.4 Aminoácidos
- 35.1 Condensation polymerisation · 35.1 Polimerización por condensación
- 35.2 Predicting the type of polymerisation · 35.2 Predecir el tipo de polimerización
- 35.3 Degradable polymers · 35.3 Polímeros degradables
- 36.1 Organic synthesis · 36.1 Síntesis orgánica
- 37.1 Thin-layer chromatography · 37.1 Cromatografía en capa fina
- 37.2 Gas/liquid chromatography · 37.2 Cromatografía de gases/líquidos
- 37.3 Carbon-13 NMR spectroscopy · 37.3 Espectroscopía RMN de carbono-13
- 37.4 Proton (1H) NMR spectroscopy · 37.4 Espectroscopía RMN de protones (¹H)
Presentation slides · Diapositivas de presentación · A-Level Chemistry · A-Level Química (37)
- 1. Atomic structure · 1. Estructura atómica
- 2. Atoms, molecules and stoichiometry · 2. Átomos, moléculas y estequiometría
- 3. Chemical bonding · 3. Enlace químico
- 4. States of matter · 4. Estados de la materia
- 5. Chemical energetics · 5. Energetica química
- 6. Electrochemistry · 6. Electroquímica
- 7. Equilibria · 7. Equilibrios
- 8. Reaction kinetics · 8. Cinética de reacción
- 9. The Periodic Table: chemical periodicity · 9. La Tabla Periódica: periodicidad química
- 10. Group 2 · 10. Grupo 2
- 11. Group 17 · 11. Grupo 17
- 12. Nitrogen and sulfur · 12. Nitrógeno y azufre
- 13. An introduction to AS Level organic chemistry · 13. Una introducción a la química orgánica AS Level
- 14. Hydrocarbons · 14. Hidrocarburos
- 15. Halogen compounds · 15. Compuestos halogenados
- 16. Hydroxy compounds · 16. Compuestos hidroxilados
- 17. Carbonyl compounds · 17. Compuestos carbonilo
- 18. Carboxylic acids and derivatives · 18. Ácidos carboxílicos y derivados
- 19. Nitrogen compounds · 19. Compuestos de nitrógeno
- 20. Polymerisation · 20. Polimerización
- 21. Organic synthesis · 21. Síntesis orgánica
- 22. Analytical techniques · 22. Técnicas analíticas
- 23. Chemical energetics · 23. Energetica química
- 24. Electrochemistry · 24. Electroquímica
- 25. Equilibria · 25. Equilibrios
- 26. Reaction kinetics · 26. Cinética de reacción
- 27. Group 2 · 27. Grupo 2
- 28. Chemistry of transition elements · 28. Química de elementos de transición
- 29. An introduction to A Level organic chemistry · 29. Una introducción a la química orgánica A Level
- 30. Hydrocarbons · 30. Hidrocarburos
- 31. Halogen compounds · 31. Compuestos halogenados
- 32. Hydroxy compounds · 32. Compuestos hidroxilados
- 33. Carboxylic acids and derivatives · 33. Ácidos carboxílicos y derivados
- 34. Nitrogen compounds · 34. Compuestos de nitrógeno
- 35. Polymerisation · 35. Polimerización
- 36. Organic synthesis · 36. Síntesis orgánica
- 37. Analytical techniques · 37. Técnicas analíticas
Course units and learning goals · Unidades del curso y objetivos de aprendizaje
These lessons teach selected course objectives. Check the remaining coverage gaps; the material is not a complete preparation programme. · Estas lecciones enseñan objetivos del curso seleccionados. Revisa los vacíos de cobertura restantes; el material no es un programa completo de preparación.
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 · enlace iónico
- 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 · enlace iónico
- 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 · enlace iónico
- 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 · enlace iónico
- 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 · enlace iónico
- 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 · enlace iónico
- 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 · enlace iónico
- 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 · exotérmica
- 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 · exotérmica
- 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 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 · punto de equivalencia
- 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 · velocidad
- 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 · equilibrio
- 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 · punto de equivalencia
- 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 · reducción
- 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 · Preparación para esta cualificación
- 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 20 h plus collaborative sciences project 10 h and investigation 10 h; use the current chemistry data booklet.
Teaching coverage still needed · Cobertura docente aún necesaria
- Full 2025 SL 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 · Especificaciones y documentos de muestra
- Chemistry — Subject brief · 2025 ↗
First assessment: 2025
- IB Chemistry guide first assessment 2025 ↗
Course materials · Materiales del curso
- Study notes · Notas de estudio →
- Revision questions · Preguntas de repaso →
- Teaching guidance · Guía docente · Teacher access · Acceso del profesor →
- Teacher diagnostics · Diagnóstico del profesor · Teacher access · Acceso del profesor →
- Supervised task guidance · Guía de tareas supervisadas · Teacher access · Acceso del profesor →
Course preparation · Preparación del curso
Documents are available. Board-specific notes, assessments and interactive past-paper practice are not yet available for every course. · Los documentos están disponibles. Las notas específicas de la entidad evaluadora, las evaluaciones y la práctica interactiva deantiguos exámenes no están disponibles aún para todos los cursos.
Lessons · Lecciones →