1. Structure, Bonding & Introduction to Organic Chemistry

1.1 Formulae & Equations

1.1.1 Formulae & Mass

1.1.2 Avogadro & the Mole

1.1.3 Full & Ionic Equations

1.1.4 Calculating Formulae

1.2 Amount of Substance

1.2.1 Concentration Calculations

1.2.2 Reacting Mass Calculations

1.2.3 Reacting Volume Calculations

1.2.4 Calculations of Product

1.3 Atomic Structure

1.3.1 Sub-Atomic Particles

1.3.2 Isotopes & Mass Spectra

1.4 Electrons & Ions

1.4.1 Endothermic Ionisation Energy

1.4.2 Electronic Structures

1.4.3 Shapes of Orbitals

1.4.4 Electronic Configurations & Chemical Properties

1.5 The Periodic Table

1.5.1 Periodicity - Ionisation Energy

1.5.2 Periodicity - Thermal Trends

1.6 Ionic & Metallic Bonding & Structure

1.6.1 Evidence of Ions

1.6.2 Ionic Bonding & Structures

1.6.3 Ionic Bond Strength

1.6.4 Polarisation

1.6.5 Metallic Bonding & Lattices

1.7 Covalent Bonding & Structure

1.7.1 Evidence of Covalent Bonding

1.7.2 Covalent Bonding

1.7.3 Carbon Allotropes

1.7.6 Predicting Shapes & Angles

1.8 Introductory Organic Chemistry

1.8.2 Functional Groups & Homologous Series

1.8.3 Nomenclature & Classification

1.8.4 Isomers - Structural

1.9 Alkanes

1.9.1 Alkanes - Introduction

1.9.2 Alkanes as Fuels

1.9.3 Combustion of Alkanes

1.9.4 Alternative Fuels

1.9.5 Free Radicals & Fission

1.9.6 The Free Radical Substitution Mechanism

1.10 Alkenes

1.10.1 Alkenes - Introduction

1.10.2 Isomers - Geometric

1.10.3 Reactions of Alkenes

1.10.4 Saturation Test

1.10.5 Electrophilic Addition - Mechanism

1.10.6 Addition Polymerisation

1.10.7 Polymer Disposal

2. Energetics, Group Chemistry, Halogenoalkanes & Alcohols

2.1 Energetics

2.1.1 Enthalpy Level Diagrams

2.1.2 Enthalpy Change - Definitions

2.1.3 Using Calorimetry

2.1.4 Using Hess Cycles

2.1.5 Bond Enthalpies

2.2 Intermolecular Forces

2.2.1 Intermolecular Forces - Introduction

2.2.2 Hydrogen Bonding

2.2.3 Physical Properties

2.2.4 Solvent Choice

2.3 Redox Chemistry & Acid-Base Titrations

2.3.1 Oxidation Numbers - Introduction

2.3.2 Oxidation & Reduction

2.3.3 Disproportionation Reactions

2.3.4 Ionic Equations

2.3.5 Acid-Base Titrations with Indicators

2.4 Groups 1 & 2

2.4.1 Ionisation Energy - Groups 1 & 2

2.4.2 Reactivity - Groups 1 & 2

2.4.3 Oxides & Hydroxides

2.4.4 Group 2 Hydroxides & Sulfates

2.4.5 Nitrates & Carbonates

2.4.6 Flame Tests

2.4.7 Qualitative Tests

2.5 Group 7

2.5.1 Trends of the Group 7 Elements

2.5.2 Halogen Displacement Reactions

2.5.3 Redox Reactions of the Halogens

2.5.4 Other Reactions of the Halogens

2.6 Introduction to Kinetics & Equilibria

2.6.1 Collision Theory

2.6.2 Rates of Reaction

2.6.3 Maxwell-Boltzmann Distributions

2.6.4 Catalysts & Energy

2.6.5 Dynamic Equilibrium in Reversible Reactions

2.6.6 Le Chatelier's Principle

2.6.7 Industrial Compromises

2.7 Organic Chemistry: Introduction

2.7.1 Types of Reaction

2.7.2 Reaction Mechanisms: Introduction

2.8 Organic Chemistry: Halogenoalkanes

2.8.1 Halogenoalkanes - Introduction

2.8.2 Reactions of Halogenoalkanes

2.8.3 The Nucleophilic Substitution Mechanism

2.8.4 Hydrolysis of Halogenoalkanes

2.8.5 Trends in Halogenoalkanes

2.9 Organic Chemistry: Alcohols

2.9.1 Alcohols - Introduction

2.9.2 Reactions of Alcohols

2.9.3 Oxidation of Alcohols

2.10 Organic Chemistry: Techniques & Spectra

2.10.1 Organic Chemistry Techniques

2.10.2 Interpreting Mass Spectra

2.10.3 Using Infrared Spectrometry

3. Practical Skills in Chemistry I

3.1 Physical Chemistry Core Practicals

3.1.1 Molar Volume of a Gas

3.1.2 Determining Enthalpy Change of Reaction

3.1.3 Determining Concentrations

3.1.4 Standard Solutions

3.2 Inorganic & Organic Chemistry Core Practicals

3.2.1 Hydrolysis of Halogenoalkanes

3.2.2 Chlorination of 2-Methylpropan-2-ol

3.2.3 Propan-1-ol Oxidation

3.2.4 AS Qualitative Analysis