14. Hydrocarbons
14.1 Alkanes 14.2 Alkenes Download PDF 14.1 Alkanes Download PDF 14.2 Alkenes
14.1 Alkanes 14.2 Alkenes Download PDF 14.1 Alkanes Download PDF 14.2 Alkenes
Download PDF 13.1 Formula, functional group, and naming of organic compounds Download PDF 13.3 Shapes of Organic Compounds Download PDF 13.4 Isomerism
Download PDF 12 Nitrogen and Sulphur
Download PDF 11.1 Group 11- Physical properties Download PDF 11.2 Group 11- properties of halogens and hydrogen halides Download PDF 11.3 reactions of halide ions
Download PDF 10. Group 2
Download PDF 9.1 Physical Properties of period 3 elements Download PDF 9.2 Chemical properties of period 3 elements
Download PDF 8.1 Rate of reaction Download PDF 8.2 Effect of temperature Download PDF 8.3 Catalysts
Download PDF 7.1 Equilibrium Download PDF 7.2 Bronsted Lowry Theory of Acids and Bases
Download PDF 6.1 Redox processes
Download PDF 4.1 The gaseous state Download PDF 4.2 Bonding and Structure
Download 3.1 Electronegativity Download PDF 3.2 Ionic Bonding Download PDF 3.3 Metallic Bonding Download PDF 3.4 Covalent and Coordinate bonding Download PDF 3.5 Shapes of Molecules Download PDF 3.6 Intermolecular forces
Download 2.1 Relative masses Download 2.2 The mole Download 2.3 Formulae Download 2.4 Reacting Volumes and Masses
1.1 Particles in the Atom & Atomic Radius Download 1.2 Isotopes Download 1.3 Electrons, energy levels, and atomic orbitals Download 1.4 Ionization Energy
Learning outcomesCandidates should be able to: Unsaturated hydrocarbons: compounds of hydrogen and carbon only whose molecules contain carbon-to-carbon double bonds (or triple bonds) Preparations From a halogenoalkanes (dehydrohalogenation – elimination) Dehydration of an alcohol Addition of halogen, X2 Use of aqueous bromine to show the presence of a C=C bond Properties Electrophilic addition The double…