Did you know there are six primary examination boards in the UK? The three most popular are AQA, Pearson Edexcel, and OCR, followed by CIE, Eduqas and WJEC. If you’re studying or teaching Eduqas or WJEC, you can still get loads of value from your subscription as there is a lot of similarity and overlap between all the examination boards. To help you out, we’ve created a handy table of contents so you can find and jump to everything you need in just a few clicks.
Topic | Eduqas specification | Reference document | Additional content required |
---|---|---|---|
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Core Ideas, Principles and Concepts |
| |
C1 |
The language of chemistry and structure of matter |
| |
C1.1 |
Formulae and equations |
|
|
C1.2 |
Basic idea about atoms |
|
Radioactivity, atomic emission spectrum of the hydrogen atom, order of increasing energy of infrared, visible and ultraviolet light &Lyman series |
C1.3 |
Chemical calculations |
Edexcel: 16. Redox equilibria (Calculating the uncertainties in measurements) |
Cell |
C1.4 |
Bonding |
intermediate character of many bonds between purely ionic and purely covalent |
|
C1.5 |
Solid structures |
Cell | |
C1.6 |
The periodic table |
CIE: 09. The periodic table: chemical periodicity |
Cell |
C2 |
Chemical change |
Cell | Cell |
C2.1 |
Simple equilibria and acid-base reactions |
AQA: 06. Chemical Equilibria, Le Chatelier’s principle and Kc |
Cell |
C2.2 |
Thermochemistry |
Cell | |
C2.3 |
Rates of reaction |
Cell | |
C2.4 |
The wider impact of chemistry |
N/A |
Cell |
C3 |
Chemistry of carbon compounds |
Cell | Cell |
C3.1 |
Organic compounds |
Cell | |
C3.2 |
Hydrocarbons |
AQA: 19. Introduction to organic chemistry |
Cell |
C3.3 |
Halogenoalkanes |
CIE: 38. Chromatography and qualitative analysis (test for halogenoalkanes) |
Cell |
C3.4 |
Alcohols and carboxylic acids |
|
reaction of carboxylic acids with hydrogen carbonates |
C3.5 |
Instrumental analysis |
OCR: 21. Analytical techniques |
Cell |
Cell |
Physical and Inorganic chemistry |
Cell | Cell |
PI1 |
Electrochemistry |
Cell | Cell |
PI1.1
PI1.2 |
Redox and standard electrode potential Redox reactions |
Cell | |
PI2 |
More complex patterns of the Periodic Table |
Cell | Cell |
PI2.1 |
Chemistry of the p-block |
CIE: 09. The periodic table: chemical periodicity |
Group 3 elements, properties of CO2 and PbO, Bonding in group 4 chlorides and their reaction with water |
PI2.2 |
Chemistry of the d-block transition metals |
|
Cell |
PI3 |
Chemical kinetics |
Cell | |
PI4 |
Energy changes |
Cell | Cell |
PI4.1 |
Enthalpy changes for solids and solutions |
Cell | |
PI4.2 |
Entropy and feasibility of reactions |
Cell | |
PI5 |
Equilibria |
Cell | Cell |
PI5.1 |
Equilibrium constants |
Cell | |
PI5.2 |
Acid-base equilibria |
Cell | |
Cell |
ORGANIC CHEMISTRY AND ANALYSIS |
Cell | Cell |
OA1 |
Higher concepts in organic chemistry |
Cell | Cell |
OA1.1 |
Stereoisomerism |
AQA: 19. Introduction to organic chemistry (E-Z isomerism) |
Cell |
OA1.2 |
Aromaticity |
CIE: 15. Hydrocarbons (Electrophilic substitution of benzene) |
Cell |
OA2 |
Organic compounds containing oxygen |
Cell | Cell |
OA2.1 |
Alcohols and phenols |
AQA: 21. Halogenoalkanes (forming primary and secondary alcohols from halogenoalkanes) AQA: 26. Aldehydes and ketones (forming primary and secondary alcohols from carbonyl compounds) |
FeCl3(aq) test for phenols |
OA2.2 |
Aldehydes and ketones |
addition of HCN to propanone |
|
OA2.3 |
Carboxylic acids and their derivatives |
CIE: 19. Carboxylic acids and derivatives Edexcel: 28. Carboxylic acids (Reduction of carboxylic acids) CIE: 15. Hydrocarbons (Oxidation of side chains in arenes) OCR: 36. Carbon-carbon bond formation |
Cell |
OA3 |
Organic compounds containing nitrogen |
Cell | Cell |
OA3.1 |
Amines |
reaction of primary amines (aliphatic) with cold nitric(III) acid,origin of colour in terms of the wavelengths of visible light absorbed |
|
OA3.2 |
Amino acids, peptides and proteins |
Cell | |
OA4 |
Organic synthesis and analysis |
AQA: 33. Nuclear magnetic resonance spectroscopy |
Cell |