Module 1 · syllabus 11.1, 11.2
Naming organic molecules
What does a name tell you about a molecule?
This module is planned. It will have readings, an experiment, practice with self-checks and a final check.
Topic 11 of 12 · 5 modules planned
Carbon compounds: naming them, fuels from crude oil, and the families that build plastics.
Module 1 · syllabus 11.1, 11.2
What does a name tell you about a molecule?
This module is planned. It will have readings, an experiment, practice with self-checks and a final check.
Core for every pupil · Supplement also for Extended entry. Paraphrased from the Cambridge IGCSE Chemistry 0620 syllabus (2026–2028); check the official syllabus for exact wording.
11.1.1Displayed formula: all atoms and bondsC11.1.2General formulae: alkane, alkene, alcohol, carboxylic acidC11.1.3Functional groups and chemical familyC11.1.4Homologous series and shared chemistryC11.1.5Saturated carbon chainsC11.1.6Unsaturated carbon chainsC11.1.7Unambiguous structural formulaeS11.1.8Structural isomers: C4H10 and C4H8S11.1.9Series features: group, formula, CH2 step, physical trend, chemistryS11.2.1Core names and displayed structures, including reaction productsC11.2.2Family recognition from suffix, formula or structureC11.2.3Unbranched families through C4, including position namesS11.2.4Ester names and structures from alcohol/acid pairs through C4S11.3.1Coal, natural gas and petroleumC11.3.2Methane in natural gasC11.3.3Hydrocarbon classificationC11.3.4Petroleum as a hydrocarbon mixtureC11.3.5Petroleum fractional distillationC11.3.6Fraction trends: chain length, volatility, boiling, viscosityC11.3.7Eight petroleum fractions and their usesC11.4.1Alkane single bonds and saturationC11.4.2Alkane reactivity: combustion and chlorine substitutionC11.4.3Substitution as atom/group replacementS11.4.4UV-initiated alkane monochlorinationS11.5.1Alkene C=C and unsaturationC11.5.2Catalytic cracking into alkenes/hydrogenC11.5.3Why cracking is usedC11.5.4Aqueous bromine test for unsaturationC11.5.5Addition and one-product formationS11.5.6Alkene additions: bromine, hydrogen/Ni, steam/acidS11.6.1Ethanol routes: fermentation and ethene hydrationC11.6.2Ethanol combustionC11.6.3Ethanol as solvent and fuelC11.6.4Comparing ethanol production routesS11.7.1Ethanoic acid with metal, base and carbonateC11.7.2Ethanol oxidation by reagent or bacteriaS11.7.3Acid-catalysed esterificationS11.8.1Monomers and large polymer moleculesC11.8.2Ethene addition to poly(ethene)C11.8.3Plastic materials and polymersC11.8.4Plastic properties and disposalC11.8.5Landfill, ocean accumulation and toxic combustion productsC11.8.6Addition/condensation repeat units and linkagesS11.8.7Alkene monomer ↔ addition repeat unitS11.8.8Diacid+diamine/diol ↔ condensation polymerS11.8.9Addition versus condensation polymerisationS11.8.10Nylon and PET structuresS11.8.11PET depolymerisation and re-polymerisationS11.8.12Amino-acid monomers and natural polyamidesS11.8.13Protein polymer structureS