Specification points
OCR A-level Chemistry B (Salters) H433
389 points in 14 topics, with OCR's codes and titles.
Grade boundaries·OCR command words
Codes and titles are read by a script from OCR's published specification and have not been checked by a person. What each point covers is in the specification itself: OCR’s specification.
1 Development of practical skills in chemistry
- 1.1 Practical skills assessed in a written examination
- 1.1.1 Planning
- 1.1.1(a) Designing experiments to solve practical problems
- 1.1.1(b) Identifying variables to control
- 1.1.1(c) Judging whether a method suits the aims
- 1.1.2 Implementing
- 1.1.2(a) Using practical apparatus and techniques correctly
- 1.1.2(b) Units for measurements
- 1.1.2(c) Presenting observations and data
- 1.1.3 Analysis
- 1.1.3(a) Processing and interpreting experimental results
- 1.1.3(b) Maths skills for analysing quantitative data
- 1.1.3(c) Significant figures
- 1.1.3(d) Plotting and interpreting graphs of results
- 1.1.3(d)(i) Choosing and labelling graph axes
- 1.1.3(d)(ii) Gradients and intercepts from graphs
- 1.1.4 Evaluation
- 1.1.4(a) Evaluating results and drawing conclusions
- 1.1.4(b) Spotting anomalies in measurements
- 1.1.4(c) Limitations of experimental procedures
- 1.1.4(d) Precision, accuracy, errors and uncertainties
- 1.1.4(e) Improving experimental procedures and apparatus
- 1.2 Practical skills assessed in the practical endorsement
- 1.2.1 Practical skills
- 1.2.1(a) Investigative approaches in practical work
- 1.2.1(b) Safe, correct use of practical equipment
- 1.2.1(c) Following written instructions
- 1.2.1(d) Making and recording observations and measurements
- 1.2.1(e) Keeping records of practical activities
- 1.2.1(f) Presenting information and data scientifically
- 1.2.1(g) Software and tools for data and research
- 1.2.1(h) Research skills using online and printed sources
- 1.2.1(i) Citing sources of information
- 1.2.1(j) Range of practical instruments and techniques
- 1.2.2 Use of apparatus and techniques
- 1.2.2(a) Apparatus for measuring mass, time, volume and temperature
- 1.2.2(b) Heating with water baths, heaters or sand baths
- 1.2.2(c) Measuring pH
- 1.2.2(d) Laboratory techniques: titration, reflux, tests and filtration
- 1.2.2(d)(i) Titration with burette and pipette
- 1.2.2(d)(ii) Reflux and distillation apparatus
- 1.2.2(d)(iii) Qualitative tests for ions and functional groups
- 1.2.2(d)(iv) Filtration techniques
- 1.2.2(e) Making a standard solution
- 1.2.2(f) Acid–base indicators in titrations
- 1.2.2(g) Purifying solid and liquid products
- 1.2.2(g)(i) Recrystallising a solid product
- 1.2.2(g)(ii) Purifying a liquid with a separating funnel
- 1.2.2(h) Melting point apparatus
- 1.2.2(i) Thin layer or paper chromatography
- 1.2.2(j) Electrochemical cells and measuring voltages
- 1.2.2(k) Safe handling of hazardous substances
- 1.2.2(l) Measuring rates of reaction
- 1.2.2(l)(i) Initial rate methods such as clock reactions
- 1.2.2(l)(ii) Continuous monitoring of reaction rate
EL Elements of life
- EL(a) Atomic structure and relative mass terms
- EL(b) Mole calculations for masses, with practical work
- EL(b)(i) Mole calculations: masses, formulae and yields
- EL(b)(ii) Measuring masses of solids
- EL(c) Concentration calculations and titrations
- EL(c)(i) Mole calculations: concentration and titrations
- EL(c)(ii) Measuring volumes and preparing standard solutions
- EL(d) Full and ionic equations with state symbols
- EL(e) Representing electrons in orbitals
- EL(f) Electron configurations using sub-shells
- EL(f)(i) Configurations of atoms from hydrogen to krypton
- EL(f)(ii) Configurations of s- and p-block ions
- EL(f)(iii) Outer sub-shells of other periods
- EL(g) Developing models of the atom
- EL(h) Nuclear fusion and element formation
- EL(i) Bonding and dot-and-cross diagrams
- EL(j) Giant lattice and simple molecular structures
- EL(k) Shapes of molecules and ions
- EL(l) Sodium chloride type lattices
- EL(m) The periodic table and predicting properties
- EL(n) Melting point trends in Periods 2 and 3
- EL(o) Ion charges and formulae of common ions
- EL(p) Group 2 elements and compounds
- EL(q) Ionisation enthalpy and its trends
- EL(r) Charge density and carbonate stability
- EL(s) Solubility of salts and tests for ions
- EL(t) Acids, bases and making salts
- EL(u) Basic Group 2 oxides and hydroxides
- EL(v) Order of the electromagnetic spectrum
- EL(w) Atomic spectra and electron transitions
- EL(w)(i) Absorption and emission spectra
- EL(w)(ii) Features of atomic spectra
- EL(w)(iii) Energy and frequency: ∆E = hν
- EL(w)(iv) Frequency, wavelength and speed of light
- EL(w)(v) Flame colours of metal ions
- EL(x) Relative atomic mass from mass spectra
DF Developing fuels
- DF(a) Mole calculations for gases, equations and enthalpy
- DF(b) Sigma and pi bonds in organic compounds
- DF(c) Molecular shape and 3-D wedge diagrams
- DF(d) Enthalpy change terms
- DF(e) Bond enthalpy and overall enthalpy change
- DF(f) Measuring energy transferred in reactions
- DF(g) Hess' law enthalpy cycles
- DF(h) Catalysis terms
- DF(i) How heterogeneous catalysts work
- DF(j) Catalytic cracking
- DF(k) Atmospheric pollutants from fuels
- DF(l) Organic classification terms
- DF(m) Naming alkanes, cycloalkanes, alkenes and alcohols
- DF(n) Combustion equations for organic compounds
- DF(o) Addition reactions of alkenes
- DF(o)(i) Bromine addition and testing for unsaturation
- DF(o)(ii) Addition of hydrogen bromide
- DF(o)(iii) Hydrogenation to alkanes
- DF(o)(iv) Hydration to alcohols
- DF(p) Addition polymers and their monomers
- DF(q) Electrophilic addition mechanism and its evidence
- DF(r) Full, shortened and skeletal formulae
- DF(s) Structural isomerism
- DF(t) E/Z and cis/trans isomerism
- DF(t)(i) E/Z naming of isomers
- DF(t)(ii) Cis/trans naming of isomers
- DF(u) Fossil fuels, biofuels and hydrogen compared
ES Elements from the sea
- ES(a) Atom economy
- ES(b) Extracting halogens from seawater
- ES(c) Electrolysis and electrode half-equations
- ES(c)(i) Products at the anode
- ES(c)(ii) Products at the cathode
- ES(d) Redox as electron transfer
- ES(d)(i) Half-equations for oxidation and reduction
- ES(d)(ii) Oxidation and reduction as electron loss and gain
- ES(d)(iii) Oxidising and reducing agents
- ES(e) Oxidation states in redox reactions
- ES(f) Balancing redox equations and iodine–thiosulfate titrations
- ES(g) Naming inorganic compounds
- ES(h) Physical properties of the halogens
- ES(i) Relative reactivity of the halogens
- ES(j) Halogen displacement reactions
- ES(k) Silver halide precipitates and ammonia
- ES(l) Preparing hydrogen halides
- ES(m) Properties of hydrogen halides
- ES(n) Chlorine: risks and uses
- ES(o) Features of dynamic equilibrium
- ES(p) The equilibrium constant Kc
- ES(q) Kc, concentration, temperature and pressure
OZ The ozone story
- OZ(a) Electronegativity and bond polarity
- OZ(b) Instantaneous and permanent dipole bonds
- OZ(c) Hydrogen bonding in water and ice
- OZ(d) Boiling points and intermolecular bonds
- OZ(e) Activation enthalpy and enthalpy profiles
- OZ(f) Collision theory and factors affecting rate
- OZ(g) Catalysts lowering activation enthalpy
- OZ(h) Homogeneous catalysis and intermediates
- OZ(i) Gas composition in percent and ppm
- OZ(j) Haloalkanes and amines as homologous series
- OZ(j)(i) Haloalkanes and their naming
- OZ(j)(ii) Amines
- OZ(k) Properties of haloalkanes
- OZ(k)(i) Boiling points of haloalkanes
- OZ(k)(ii) Nucleophilic substitution of haloalkanes
- OZ(l) Substitution and nucleophiles
- OZ(m) The SN2 mechanism
- OZ(n) Haloalkane reactivity: bond enthalpy or polarity
- OZ(o) Homolytic and heterolytic fission
- OZ(p) Radicals and radical mechanisms
- OZ(p)(i) Radical chain reaction steps
- OZ(p)(ii) Radical halogenation of alkanes
- OZ(p)(iii) Half curly arrows
- OZ(q) Haloalkanes and ozone depletion
- OZ(r) Ozone in the stratosphere and troposphere
- OZ(r)(i) Ozone as a sunscreen against UV
- OZ(r)(ii) Ozone pollution and photochemical smog
- OZ(s) Radiation from the Earth and Sun
- OZ(t) UV and visible light exciting electrons
- OZ(u) Frequency, wavelength and energy calculations
WM What’s in a medicine?
- WM(a) Homologous series in medicines chemistry
- WM(b) Classifying alcohols by structure
- WM(c) Properties of phenols
- WM(c)(i) Acidity of phenols
- WM(c)(ii) Iron(III) chloride test for phenols
- WM(c)(iii) Phenols with acid anhydrides
- WM(d) Reactions of alcohols in synthesis
- WM(d)(i) Esterification of alcohols
- WM(d)(ii) Oxidation of alcohols with dichromate
- WM(d)(iii) Dehydration of alcohols to alkenes
- WM(d)(iv) Alcohols to haloalkanes
- WM(e) Making and purifying an organic solid
- WM(f) Making and purifying an organic liquid
- WM(g) Green chemistry in industry
- WM(h) Elimination reactions
- WM(i) Interpreting mass spectra
- WM(i)(i) Molecular ion peak
- WM(i)(ii) Fragment ion peaks
- WM(i)(iii) The M+1 peak and carbon-13
- WM(j) Infrared spectra and functional groups
CI The chemical industry
- CI(a) Rate terms and rate equations
- CI(a)(i) Rate of reaction
- CI(a)(ii) Rate constant and units
- CI(a)(iii) Order of reaction
- CI(a)(iv) Rate equations
- CI(b) Half-life calculations
- CI(c) Finding orders and rate equations experimentally
- CI(d) The Arrhenius equation
- CI(e) Rate-determining step and mechanisms
- CI(f) Temperature, pressure and catalysts on Kc
- CI(g) Economical conditions for industrial processes
- CI(h) Kc calculations and experiments
- CI(i) Reactions in industrial processes
- CI(j) Nitrogen chemistry
- CI(j)(i) Bonding in nitrogen, ammonia and ammonium
- CI(j)(ii) Oxides of nitrogen
- CI(j)(iii) Interconverting nitrogen species
- CI(j)(iv) Tests for nitrate and ammonium ions
- CI(k) Costs, benefits and risks of industrial processes
- CI(k)(i) Costs of industrial processes
- CI(k)(ii) Benefits and hazards of industrial processes
PL Polymers and life
- PL(a) Amino acids, proteins and paper chromatography
- PL(a)(i) Amino acids, peptide links and proteins
- PL(a)(ii) Paper chromatography
- PL(b) Protein structure and intermolecular bonds
- PL(c) Nucleic acids as condensation polymers of nucleotides
- PL(c)(i) Phosphate–sugar backbone
- PL(c)(ii) Bases joining the backbone
- PL(c)(iii) The DNA double helix and base pairing
- PL(d) Base pairing, replication and protein coding
- PL(e) Molecular recognition in drug action
- PL(e)(i) Pharmacophores
- PL(e)(ii) Drug binding to receptor sites
- PL(e)(iii) Three-dimensional interactions between species
- PL(f) Enzyme rate and substrate concentration
- PL(g) Characteristics of enzyme catalysis
- PL(h) Acidity of carboxylic acids
- PL(i) Amino acids as zwitterions
- PL(j) Basicity of amines
- PL(k) Naming organic families and nylons
- PL(l) Primary and secondary amide groups
- PL(m) Hydrolysis of esters and amides
- PL(n) Acyl chlorides with amines and alcohols
- PL(o) Addition and condensation polymerisation compared
- PL(p) Condensation polymers and their monomers
- PL(q) Optical isomerism and chirality
- PL(q)(i) Drawing optical stereoisomers
- PL(q)(ii) Chiral molecules and chiral centres
- PL(q)(iii) Enantiomers
- PL(r) Further interpretation of mass spectra
- PL(r)(i) Molecular formula from a high-resolution M⁺ peak
- PL(r)(ii) Fragment losses from peak differences
- PL(s) Proton and carbon-13 NMR
- PL(t) Combining spectroscopic techniques
O Oceans
- O(a) Solubility in aqueous and non-aqueous solvents
- O(b) Enthalpy of solution, lattice and hydration terms
- O(b)(i) Enthalpy cycles for dissolving ionic solids
- O(b)(ii) Calculations with dissolving enthalpy cycles
- O(b)(iii) Measuring enthalpy changes in solution
- O(c) Charge density, lattice and hydration enthalpies
- O(d) Entropy and arrangements of energy quanta
- O(e) Predicting entropy changes qualitatively
- O(e)(i) Entropy of solids, liquids and gases
- O(e)(ii) Gaseous particle numbers and entropy
- O(f) Total entropy change and feasibility
- O(g) Calculating system entropy change
- O(h) Solubility products
- O(i) Brønsted–Lowry theory
- O(i)(i) Proton donors and acceptors
- O(i)(ii) Identifying donors and acceptors in reactions
- O(i)(iii) Conjugate acids and bases
- O(j) Strong acids and strong bases
- O(k) Weak acids, Kₐ and pKₐ
- O(l) pH calculations
- O(l)(i) pH of strong acids
- O(l)(ii) pH of strong bases using Kw
- O(l)(iii) pH of weak acids
- O(m) Buffer solutions
- O(m)(i) What a buffer is
- O(m)(ii) How buffers work
- O(m)(iii) Buffer calculations
- O(n) The greenhouse effect
- O(n)(i) Solar radiation reaching Earth
- O(n)(ii) Earth radiating infrared
- O(n)(iii) Greenhouse gases absorbing infrared
- O(n)(iv) How absorbed infrared raises temperature
- O(n)(v) Re-emission of infrared by greenhouse gases
- O(n)(vi) The enhanced greenhouse effect
DM Developing metals
- DM(a) Manganate(VII) and other titrations
- DM(b) Coordination number and complex shapes
- DM(c) Balancing redox equations with acid–base steps
- DM(d) Simple electrochemical cells
- DM(d)(i) Metal ion/metal half-cells
- DM(d)(ii) Half-cells with inert electrodes
- DM(d)(iii) Setting up electrochemical cells
- DM(e) How an electrochemical cell works
- DM(f) Standard electrode potentials and their uses
- DM(f)(i) Calculating Ecell
- DM(f)(ii) Predicting feasibility of redox reactions
- DM(f)(iii) Rusting and its prevention
- DM(g) Transition metals, iron and copper ions
- DM(h) d-block configurations and variable oxidation states
- DM(i) Ligands, complexes and ligand substitution
- DM(j) Complex formation and polydentate ligands
- DM(k) Iron and copper ions with hydroxide and ammonia
- DM(l) Transition metals as catalysts
- DM(m) Colour in transition metal complexes
- DM(m)(i) Coloured transition metal ions
- DM(m)(ii) d-orbital splitting and colour
- DM(n) Colorimetry and spectrophotometry
CD Colour by design
- CD(a) How dyes attach to fibres
- CD(b) Dye structure and the chromophore
- CD(b)(i) Groups modifying the chromophore
- CD(b)(ii) Groups affecting dye solubility
- CD(b)(iii) Groups bonding dyes to fibres
- CD(c) Fats and oils as esters
- CD(d) Arenes and delocalisation
- CD(d)(i) Delocalised electrons in arenes
- CD(d)(ii) Properties explained by delocalisation
- CD(e) Representations of benzene
- CD(e)(i) Shape of the benzene molecule
- CD(e)(ii) Bonding in benzene and hydrogenation enthalpy
- CD(f) Polyfunctional molecules and functional group tests
- CD(g) Electrophilic substitution reactions of arenes
- CD(g)(i) Halogenation of the benzene ring
- CD(g)(ii) Nitration and its mechanism
- CD(g)(iii) Sulfonation
- CD(g)(iv) Friedel–Crafts alkylation and acylation
- CD(h) Diazonium compounds and azo dyes
- CD(i) Reactions of aldehydes and ketones
- CD(i)(i) Oxidising aldehydes with dichromate
- CD(i)(ii) Fehling's and Tollens' tests
- CD(i)(iii) Cyanide addition to form cyanohydrins
- CD(j) Planning synthetic routes
- CD(k) Nucleophilic addition mechanism with cyanide
- CD(l) Classifying organic reactions and mechanisms
- CD(l)(i) Types of organic reaction
- CD(l)(ii) Describing unfamiliar mechanisms
- CD(m) Colour and UV absorption in organic molecules
- CD(n) Gas–liquid chromatography
- CD(n)(i) Sample injection into carrier gas
- CD(n)(ii) The chromatography column
- CD(n)(iii) Detecting emerging compounds
- CD(n)(iv) Retention times
CL Chemical literacy
5d How Science Works (HSW)
- HSW1 Theories and models to explain science
- HSW2 Posing questions and presenting scientific arguments
- HSW3 Methods, including ICT, to answer scientific questions
- HSW4 Experimental work and risk management
- HSW5 Analysing data, correlation and causation
- HSW6 Evaluating methods, evidence and data
- HSW7 How scientific knowledge develops over time
- HSW8 Communicating science with correct terminology
- HSW9 Applications, benefits and risks of science
- HSW10 Ethical and environmental issues in science
- HSW11 Scientific community and validating knowledge
- HSW12 Science in society's decision making
5e Mathematical requirements
- M0 Arithmetic and numerical computation
- M0.0 Units in calculations
- M0.1 Decimal and ordinary form
- M0.2 Ratios, fractions and percentages
- M0.3 Estimating results
- M0.4 Powers, exponentials and logarithms on calculators
- M1 Handling data
- M1.1 Significant figures
- M1.2 Arithmetic means
- M1.3 Uncertainties in measurements and combined data
- M2 Algebra
- M2.1 Mathematical symbols
- M2.2 Changing the subject of an equation
- M2.3 Substituting values into equations
- M2.4 Solving algebraic equations
- M2.5 Logarithms for wide-ranging quantities
- M3 Graphs
- M3.1 Graphical, numerical and algebraic forms
- M3.2 Plotting two variables from data
- M3.3 Slope and intercept of a linear graph
- M3.4 Rate of change from a linear graph
- M3.5 Tangents to curves as rates of change
- M4 Geometry and trigonometry
- M4.1 Angles and shapes in 2-D and 3-D structures
- M4.2 Representing 2-D and 3-D forms
- M4.3 Symmetry of 2-D and 3-D shapes