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Topic 11 of 12 · 5 modules planned

Organic chemistry

Carbon compounds: naming them, fuels from crude oil, and the families that build plastics.

Modules

  1. 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.

Syllabus statements for this topic · for teachers · 50 statements

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 Formulae, functional groups and terminology

  • 11.1.1Displayed formula: all atoms and bondsC
  • 11.1.2General formulae: alkane, alkene, alcohol, carboxylic acidC
  • 11.1.3Functional groups and chemical familyC
  • 11.1.4Homologous series and shared chemistryC
  • 11.1.5Saturated carbon chainsC
  • 11.1.6Unsaturated carbon chainsC
  • 11.1.7Unambiguous structural formulaeS
  • 11.1.8Structural isomers: C4H10 and C4H8S
  • 11.1.9Series features: group, formula, CH2 step, physical trend, chemistryS

11.2 Naming organic compounds

  • 11.2.1Core names and displayed structures, including reaction productsC
  • 11.2.2Family recognition from suffix, formula or structureC
  • 11.2.3Unbranched families through C4, including position namesS
  • 11.2.4Ester names and structures from alcohol/acid pairs through C4S

11.3 Fuels

  • 11.3.1Coal, natural gas and petroleumC
  • 11.3.2Methane in natural gasC
  • 11.3.3Hydrocarbon classificationC
  • 11.3.4Petroleum as a hydrocarbon mixtureC
  • 11.3.5Petroleum fractional distillationC
  • 11.3.6Fraction trends: chain length, volatility, boiling, viscosityC
  • 11.3.7Eight petroleum fractions and their usesC

11.4 Alkanes

  • 11.4.1Alkane single bonds and saturationC
  • 11.4.2Alkane reactivity: combustion and chlorine substitutionC
  • 11.4.3Substitution as atom/group replacementS
  • 11.4.4UV-initiated alkane monochlorinationS

11.5 Alkenes

  • 11.5.1Alkene C=C and unsaturationC
  • 11.5.2Catalytic cracking into alkenes/hydrogenC
  • 11.5.3Why cracking is usedC
  • 11.5.4Aqueous bromine test for unsaturationC
  • 11.5.5Addition and one-product formationS
  • 11.5.6Alkene additions: bromine, hydrogen/Ni, steam/acidS

11.6 Alcohols

  • 11.6.1Ethanol routes: fermentation and ethene hydrationC
  • 11.6.2Ethanol combustionC
  • 11.6.3Ethanol as solvent and fuelC
  • 11.6.4Comparing ethanol production routesS

11.7 Carboxylic acids

  • 11.7.1Ethanoic acid with metal, base and carbonateC
  • 11.7.2Ethanol oxidation by reagent or bacteriaS
  • 11.7.3Acid-catalysed esterificationS

11.8 Polymers

  • 11.8.1Monomers and large polymer moleculesC
  • 11.8.2Ethene addition to poly(ethene)C
  • 11.8.3Plastic materials and polymersC
  • 11.8.4Plastic properties and disposalC
  • 11.8.5Landfill, ocean accumulation and toxic combustion productsC
  • 11.8.6Addition/condensation repeat units and linkagesS
  • 11.8.7Alkene monomer ↔ addition repeat unitS
  • 11.8.8Diacid+diamine/diol ↔ condensation polymerS
  • 11.8.9Addition versus condensation polymerisationS
  • 11.8.10Nylon and PET structuresS
  • 11.8.11PET depolymerisation and re-polymerisationS
  • 11.8.12Amino-acid monomers and natural polyamidesS
  • 11.8.13Protein polymer structureS