At The Student Scoop, we provide an exceptional learning environment for AS/A Level Chemistry, ensuring you not only understand the advanced principles but also master exam techniques for top results.
Below is a detailed overview of the AS/A Level Chemistry structure to help you understand the program’s commitment and why our approach stands out.
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1. Atomic structure
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2. Atoms, molecules and stoichiometry
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3.Chemical bonding
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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 |
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4. States of matter
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5. Chemical energetics
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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)
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8. Reaction kinetics
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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 |
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10. Group 2
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11. Group 17
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12.Nitrogen and sulfur
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10.1 Similarities and trends in the properties of Group 2.
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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
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13. An introduction to AS Level organic chemistry
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14. Hydrocarbons
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15. Halogen compounds
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13.1 Formulas, functional groups and the naming of organic compounds
13.2 Characteristic organic reactionsbr 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
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16. Hydroxy compounds
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17. Carbonyl compounds
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18. Carboxylic acids and derivatives
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16.1 Alcohols
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17.1 Aldehydes and ketones
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18.1 Carboxylic acids
18.2 Esters |
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19. Nitrogen compounds
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20. Polymerisation
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21. Organic synthesis
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19.1 Primary amines
19.2 Nitriles and hydroxynitriles |
20.1 Addition polymerisation
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21.1 Organic synthesis
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22. Analytical technique
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22.1 Infrared spectroscopy
22.2 Mass spectrometry |
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1. Chemical energetics
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2. Electrochemistry
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3. Equilibria
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1.1 Lattice energy and Born-Haber cycles
1.2 Enthalpies of solution and hydration 1.3 Entropy change, ΔS 1.4 Gibbs free energy change, ΔG |
2.1 Electrolysis
2.2 Standard electrode potentials E⦵, standard cell potentials E⦵ cell and the Nernst equation |
3.1 Acids and bases
3.2 Partition coefficients |
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4. Reaction kinetics
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5. Group 2
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4.1 Simple rate equations, orders of reaction and rate constants
4.2 Homogeneous and heterogeneous catalysts |
5.1 Similarities and trends in the properties of the Group 2 metals, magnesium to barium, and
their compounds
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6.1 General physical and chemical properties of the first row of transition elements, titanium to
Copper.
6.2 General characteristic chemical properties of the first set of transition elements, titanium to Copper 6.3 Colour of complexes 6.4 Stereoisomerism in transition element complexes 6.5 Stability constants, Kstab |
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8. Hydrocarbons
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9. Halogen Compounds
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7.1 Formulas, functional groups and the naming of organic compounds
7.2 Characteristic organic reactions 7.3 Shapes of aromatic organic molecules; σ and π bonds 7.4 Isomerism: optical |
8.1 Arenes
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9.1 Halogen Compounds
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10. Hydroxy compounds
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11. Carboxylic acids and derivatives
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12. Nitrogen compounds
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10.1 Alcohols
10.2 Phenol |
11.1 Carboxylic acids
11.2 Esters 11.3 Acyl chlorides |
12.1 Primary and secondary amines
12.2 Phenylamine and azo compounds 12.3 Amides 12.4 Amino acids |
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13.Polymerisation
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14. Organic synthesis
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15. Analytical techniques
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13.1 Condensation polymerisation
13.2 Predicting the type of polymerisation 13.3 Degradable polymers |
14.1 Organic synthesis
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15.1 Thin-layer chromatography
15.2 Gas / liquid chromatography 15.3 Carbon-13 NMR spectroscopy 15.4 Proton (1H) NMR spectroscopy |
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