International Baccalaureate · IB Diploma
Chemistry · HL
Papers, samples and curriculum documents for this course. · Papers, amostras e documentos curriculares deste curso.
Handouts, exercise sheets and slides
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Handouts · Material de apoio · A-Level Chemistry · Química do A-Level (37)
- 1. Atomic structure · 1. Estrutura atômica
- 2. Atoms, molecules and stoichiometry · 2. Átomos, moléculas e estequiometria
- 3. Chemical bonding · 3. Ligação química
- 4. States of matter · 4. Estados da matéria
- 5. Chemical energetics · 5. Energetica química
- 6. Electrochemistry · 6. Eletroquímica
- 7. Equilibria · 7. Equilíbrios
- 8. Reaction kinetics · 8. Cinética de reação
- 9. The Periodic Table: chemical periodicity · 9. Tabela Periódica: periodicidade química
- 10. Group 2 · 10. Grupo 2
- 11. Group 17 · 11. Grupo 17
- 12. Nitrogen and sulfur · 12. Nitrogênio e enxofre
- 13. An introduction to AS Level organic chemistry · 13. Introdução à Química Orgânica Nível AS
- 14. Hydrocarbons · 14. Hidrocarbonetos
- 15. Halogen compounds · 15. Compostos de halogênio
- 16. Hydroxy compounds · 16. Compostos hidroxilados
- 17. Carbonyl compounds · 17. Compostos carbonila
- 18. Carboxylic acids and derivatives · 18. Ácidos carboxílicos e derivados
- 19. Nitrogen compounds · 19. Compostos nitrogenados
- 20. Polymerisation · 20. Polimerização
- 21. Organic synthesis · 21. Síntese orgânica
- 22. Analytical techniques · 22. Técnicas analíticas
- 23. Chemical energetics · 23. Energetica química
- 24. Electrochemistry · 24. Eletroquímica
- 25. Equilibria · 25. Equilíbrios
- 26. Reaction kinetics · 26. Cinética de reação
- 27. Group 2 · 27. Grupo 2
- 28. Chemistry of transition elements · 28. Química de elementos de transição
- 29. An introduction to A Level organic chemistry · 29. Introdução à Química Orgânica Nível A
- 30. Hydrocarbons · 30. Hidrocarbonetos
- 31. Halogen compounds · 31. Compostos de halogênio
- 32. Hydroxy compounds · 32. Compostos hidroxilados
- 33. Carboxylic acids and derivatives · 33. Ácidos carboxílicos e derivados
- 34. Nitrogen compounds · 34. Compostos nitrogenados
- 35. Polymerisation · 35. Polimerização
- 36. Organic synthesis · 36. Síntese orgânica
- 37. Analytical techniques · 37. Técnicas analíticas
Exercise sheets · Folhas de exercícios · A-Level Chemistry · Química do A-Level (90)
- 1.1 Particles in the atom and atomic radius · 1.1 Parteículas no átomo e raio atômico
- 1.2 Isotopes · 1.2 Isótopos
- 1.3 Electrons, energy levels and atomic orbitals · 1.3 Elétrons, níveis de energia e orbitais atômicos
- 1.4 Ionisation energy · 1.4 Energia de ionização
- 2.1 Relative masses of atoms and molecules · 2.1 Massas relativas de átomos e moléculas
- 2.2 The mole and the Avogadro constant · 2.2 O mol e a constante de Avogadro
- 2.3 Formulas · 2.3 Fórmulas
- 2.4 Reacting masses and volumes (of solutions and gases) · 2.4 Massas e volumes reagidos (de soluções e gases)
- 3.1 Electronegativity and bonding · 3.1 Eletronegatividade e ligação
- 3.2 Ionic bonding · 3.2 Ligação iônica
- 3.3 Metallic bonding · 3.3 Ligação metálica
- 3.4 Covalent bonding and coordinate (dative covalent) bonding · 3.4 Ligação covalente e ligação coordenada (covalente dative)
- 3.5 Shapes of molecules · 3.5 Formas moleculares
- 3.6 Intermolecular forces, electronegativity and bond properties · 3.6 Forças intermoleculares, eletronegatividade e propriedades das ligações
- 3.7 Dot-and-cross diagrams · 3.7 Diagramas de pontos e cruzes
- 4.1 The gaseous state: ideal and real gases and pV = nRT · 4.1 Estado gasoso: gases ideais e reais e pV = nRT
- 4.2 Bonding and structure · 4.2 Ligações e estrutura
- 5.1 Enthalpy change, ΔH · 5.1 Variação de entalpia, ΔH
- 5.2 Hess’s law · 5.2 Lei de Hess
- 6.1 Redox processes: electron transfer and changes in oxidation number (oxidation state) · 6.1 Processos redox: transferência de elétrons e alterações no número de oxidação (estado de oxidação)
- 7.1 Chemical equilibria: reversible reactions, dynamic equilibrium · 7.1 Equilíbrios químicos: reações reversíveis, equilíbrio dinâmico
- 7.2 Brønsted–Lowry theory of acids and bases · 7.2 Teoria de Brønsted–Lowry de ácidos e bases
- 8.1 Rate of reaction · 8.1 Taxa de reação
- 8.2 Effect of temperature on reaction rates and the concept of activation energy · 8.2 Efeito da temperatura nas taxas de reação e o conceito de energia de ativação
- 8.3 Homogeneous and heterogeneous catalysts · 8.3 Catalisadores homogêneos e heterogêneos
- 9.1 Periodicity of physical properties of the elements in Period 3 · 9.1 Periodicidade de propriedades físicas dos elementos no Período 3
- 9.2 Periodicity of chemical properties of the elements in Period 3 · 9.2 Periodicidade de propriedades químicas dos elementos no Período 3
- 9.3 Chemical periodicity of other elements · 9.3 Periodicidade química de outros elementos
- 10.1 Similarities and trends in the properties of the Group 2 metals, magnesium to barium, and their compounds · 10.1 Semelhanças e tendências nas propriedades dos metais do Grupo 2, magnésio a bário, e seus compostos
- 11.1 Physical properties of the Group 17 elements · 11.1 Propriedades físicas dos elementos do Grupo 17
- 11.2 The chemical properties of the halogen elements and the hydrogen halides · 11.2 Propriedades químicas dos elementos halogênios e dos hidretos halogênicos
- 11.3 Some reactions of the halide ions · 11.3 Algumas reações dos íons haluretos
- 11.4 The reactions of chlorine · 11.4 As reações do cloro
- 12.1 Nitrogen and sulfur · 12.1 Nitrogênio e enxofre
- 13.1 Formulas, functional groups and the naming of organic compounds · 13.1 Fórmulas, grupos funcionais e nomenclatura de compostos orgânicos
- 13.2 Characteristic organic reactions · 13.2 Reações orgânicas características
- 13.3 Shapes of organic molecules; σ and π bonds · 13.3 Formas de moléculas orgânicas; ligações σ e π
- 13.4 Isomerism: structural isomerism and stereoisomerism · 13.4 Isomerismo: isomerismo estrutural e estereoisomerismo
- 14.1 Alkanes · 14.1 Alcanos
- 14.2 Alkenes · 14.2 Alcenos
- 15.1 Halogenoalkanes · 15.1 Haloalcanos
- 16.1 Alcohols · 16.1 Álcoois
- 17.1 Aldehydes and ketones · 17.1 Aldeídos e cetonas
- 18.1 Carboxylic acids · 18.1 Ácidos carboxílicos
- 18.2 Esters · 18.2 Ésteres
- 19.1 Primary amines · 19.1 Aminas primárias
- 19.2 Nitriles and hydroxynitriles · 19.2 Nitrilos e hidroxonitrilos
- 20.1 Addition polymerisation · 20.1 Polimerização por adição
- 21.1 Organic synthesis · 21.1 Síntese orgânica
- 22.1 Infrared spectroscopy · 22.1 Espectroscopia Infravermelha
- 22.2 Mass spectrometry · 22.2 Espectrometria de massas
- 23.1 Lattice energy and Born-Haber cycles · 23.1 Energia reticular e ciclos de Born-Haber
- 23.2 Enthalpies of solution and hydration · 23.2 Entalpias de solução e hidratação
- 23.3 Entropy change, ΔS · 23.3 Variação de entropia, ΔS
- 23.4 Gibbs free energy change, ΔG · 23.4 Variação de energia livre de Gibbs, ΔG
- 24.1 Electrolysis · 24.1 Eletrólise
- 24.2 Standard electrode potentials E⦵, standard cell potentials E⦵cell and the Nernst equation · 24.2 Potenciais eletrodos padrão E⦵, potenciais de célula padrão E⦵cell e equação de Nernst
- 25.1 Acids and bases · 25.1 Ácidos e bases
- 25.2 Partition coefficients · 25.2 Coeficientes de partição
- 26.1 Simple rate equations, orders of reaction and rate constants · 26.1 Equações de taxa simples, ordens de reação e constantes de taxa
- 26.2 Homogeneous and heterogeneous catalysts · 26.2 Catalisadores homogêneos e heterogêneos
- 27.1 Similarities and trends in the properties of the Group 2 metals, magnesium to barium, and their compounds · 27.1 Semelhanças e tendências nas propriedades dos metais do Grupo 2, magnésio a bário, e seus compostos
- 28.1 General physical and chemical properties of the first row of transition elements, titanium to copper · 28.1 Propriedades físicas e químicas gerais da primeira série de elementos de transição, titânio a cobre
- 28.2 General characteristic chemical properties of the first set of transition elements, titanium to copper · 28.2 Propriedades químicas características gerais do primeiro conjunto de elementos de transição, titânio a cobre
- 28.3 Colour of complexes · 28.3 Cor de complexos
- 28.4 Stereoisomerism in transition element complexes · 28.4 Estereoisomerismo em complexos de elementos de transição
- 28.5 Stability constants, Kstab · 28.5 Constantes de estabilidade, Kstab
- 29.1 Formulas, functional groups and the naming of organic compounds · 29.1 Fórmulas, grupos funcionais e nomenclatura de compostos orgânicos
- 29.2 Characteristic organic reactions · 29.2 Reações orgânicas características
- 29.3 Shapes of aromatic organic molecules; σ and π bonds · 29.3 Formas de moléculas orgânicas aromáticas; ligações σ e π
- 29.4 Isomerism: optical · 29.4 Isomerismo: óptico
- 30.1 Arenes · 30.1 Arenos
- 31.1 Halogen compounds · 31.1 Compostos de halogênio
- 32.1 Alcohols · 32.1 Álcoois
- 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 Cloreto de acila
- 34.1 Primary and secondary amines · 34.1 Aminas primárias e secundárias
- 34.2 Phenylamine and azo compounds · 34.2 Fenilamina e compostos azo
- 34.3 Amides · 34.3 Amidas
- 34.4 Amino acids · 34.4 Aminoácidos
- 35.1 Condensation polymerisation · 35.1 Polimerização por condensação
- 35.2 Predicting the type of polymerisation · 35.2 Prevendo o tipo de polimerização
- 35.3 Degradable polymers · 35.3 Polímeros degradáveis
- 36.1 Organic synthesis · 36.1 Síntese orgânica
- 37.1 Thin-layer chromatography · 37.1 Cromatografia em camada fina
- 37.2 Gas/liquid chromatography · 37.2 Cromatografia gasosa/líquida
- 37.3 Carbon-13 NMR spectroscopy · 37.3 Espectroscopia NMR de Carbono-13
- 37.4 Proton (1H) NMR spectroscopy · 37.4 Espectroscopia NMR de Próton (1H)
Presentation slides · Slides de apresentação · A-Level Chemistry · Química do A-Level (37)
- 1. Atomic structure · 1. Estrutura atômica
- 2. Atoms, molecules and stoichiometry · 2. Átomos, moléculas e estequiometria
- 3. Chemical bonding · 3. Ligação química
- 4. States of matter · 4. Estados da matéria
- 5. Chemical energetics · 5. Energetica química
- 6. Electrochemistry · 6. Eletroquímica
- 7. Equilibria · 7. Equilíbrios
- 8. Reaction kinetics · 8. Cinética de reação
- 9. The Periodic Table: chemical periodicity · 9. Tabela Periódica: periodicidade química
- 10. Group 2 · 10. Grupo 2
- 11. Group 17 · 11. Grupo 17
- 12. Nitrogen and sulfur · 12. Nitrogênio e enxofre
- 13. An introduction to AS Level organic chemistry · 13. Introdução à Química Orgânica Nível AS
- 14. Hydrocarbons · 14. Hidrocarbonetos
- 15. Halogen compounds · 15. Compostos de halogênio
- 16. Hydroxy compounds · 16. Compostos hidroxilados
- 17. Carbonyl compounds · 17. Compostos carbonila
- 18. Carboxylic acids and derivatives · 18. Ácidos carboxílicos e derivados
- 19. Nitrogen compounds · 19. Compostos nitrogenados
- 20. Polymerisation · 20. Polimerização
- 21. Organic synthesis · 21. Síntese orgânica
- 22. Analytical techniques · 22. Técnicas analíticas
- 23. Chemical energetics · 23. Energetica química
- 24. Electrochemistry · 24. Eletroquímica
- 25. Equilibria · 25. Equilíbrios
- 26. Reaction kinetics · 26. Cinética de reação
- 27. Group 2 · 27. Grupo 2
- 28. Chemistry of transition elements · 28. Química de elementos de transição
- 29. An introduction to A Level organic chemistry · 29. Introdução à Química Orgânica Nível A
- 30. Hydrocarbons · 30. Hidrocarbonetos
- 31. Halogen compounds · 31. Compostos de halogênio
- 32. Hydroxy compounds · 32. Compostos hidroxilados
- 33. Carboxylic acids and derivatives · 33. Ácidos carboxílicos e derivados
- 34. Nitrogen compounds · 34. Compostos nitrogenados
- 35. Polymerisation · 35. Polimerização
- 36. Organic synthesis · 36. Síntese orgânica
- 37. Analytical techniques · 37. Técnicas analíticas
Course units and learning goals · Unidades do curso e objetivos de aprendizagem
These lessons teach selected course objectives. Check the remaining coverage gaps; the material is not a complete preparation programme. · Estas aulas ensinam objetivos selecionados do curso. Verifique as lacunas de cobertura restantes; o material não é um programa completo de preparação.
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 · ligação iônica
- 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 · ligação iônica
- 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 · ligação iônica
- 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 · ligação iônica
- 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 · ligação iônica
- 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 · ligação iônica
- 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 · ligação iônica
- 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 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 · ponto de equivalência
- 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 · taxa
- 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 · equilíbrio
- 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 · ponto de equivalência
- 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 · redução
- 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 · Preparação para esta qualificação
- 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 · Cobertura do ensino ainda necessária
- 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 · Especificações e documentos de exemplo
- Chemistry — Subject brief · 2025 ↗
First assessment: 2025
- IB Chemistry guide first assessment 2025 ↗
Course materials · Materiais do curso
- Study notes · Notas de estudo →
- Revision questions · Questões de revisão →
- Teaching guidance · Orientações de ensino · Teacher access · Acesso do professor →
- Teacher diagnostics · Diagnósticos do professor · Teacher access · Acesso do professor →
- Supervised task guidance · Orientações de tarefa supervisionada · Teacher access · Acesso do professor →
Course preparation · Preparação do curso
Documents are available. Board-specific notes, assessments and interactive past-paper practice are not yet available for every course. · Os documentos estão disponíveis. Notas específicas da banca, avaliações e prática interativa de provas anteriores ainda não estão disponíveis para todos os cursos.
Lessons · Lições →