| 0620-IGCSE-CHEMISTRY
PAPER-4-TOPIC-WISE PAST PAPERS / ORGANIC CHEMISTRY
  • 14.1-Homologous series-Set-1-qp-ms.pdf
  • 14.1-Homologous series-Set-2-qp-ms.pdf
  • 14.1-Homologous series-Set-3-qp-ms.pdf
  • 14.2-Fuels-Set-1-qp-ms.pdf
  • 14.3-Functional groups-Set-1-qp-ms.pdf
  • 14.4-Isomers-Set-1-qp-ms.pdf
  • 14.4-Isomers-Set-2-qp-ms.pdf
  • 14.5-Saturated-Unsaturated Hydrocarbons-Set-1-qp-ms.pdf
  • 14.6-Fractional distillation-Set-1-qp-ms.pdf
  • 14.7-Alkanes-Alkenes-Set-1-qp-ms.pdf
  • 14.8-Alkanes-Cracking-Set-1-qp-ms.pdf
  • 14.8-Alkanes-Cracking-Set-2-qp-ms.pdf
  • 14.9-Combustion-Set-1-qp-ms.pdf
  • 14.9-Combustion-Set-2-qp-ms.pdf
  • 14.10-Organic chem-Mixed bag-Set-1-qp-ms.pdf
  • 14.11-Alkanes-Substitution-Set-1-qp-ms.pdf
  • 14.11-Alkanes-Substitution-Set-2-qp-ms.pdf
  • 14.12-Carboxylic acids-Set-1-qp-ms.pdf
  • 14.12-Carboxylic acids-Set-2-qp-ms.pdf
  • 14.12-Carboxylic acids-Set-3-qp-ms.pdf
  • 14.13-Alcohols-Set-1-qp-ms.pdf
  • 14.14-Making ethanol-Set-1-qp-ms.pdf
  • 14.16-Chromarography-Set-1-qp-ms.pdf
  • 14.16-Petroleum fuels-Set-1-qp-ms.pdf
  • 14.17-Hydrolysis-Set-1-qp-ms.pdf
  • 14.17-Hydrolysis-Set-2-qp-ms.pdf
  • 14.18-Addition polymerisation-Set-1-qp-ms.pdf
  • 14.19-Condensation polymerisation-Set-1-qp-ms.pdf
  • 14.19-Condensation polymerisation-Set-2-qp-ms.pdf
  • 14.20-Esters-Set-1-qp-ms.pdf
Note:

IGCSE Chemistry Topic Questions Paper 4 Extended Theory for Organic Chemistry.

The exam aims to test you on the following concepts:

  • 14.1 Names of compounds

Core 

  • Name and draw the structures of methane, ethane, ethene, ethanol, ethanoic acid and the products of the reactions stated in sections 14.4–14.6 
  • State the type of compound present, given a chemical name ending in -ane, -ene, -ol, or -oic acid or a molecular structure

Supplement 

  • Name and draw the structures of the unbranched alkanes, alkenes (not cis-trans), alcohols and acids containing up to four carbon atoms per molecule 
  • Name and draw the structural formulae of the esters which can be made from unbranched alcohols and carboxylic acids, each containing up to four carbon atoms

14.2 Fuels

Core 

  • Name the fuels: coal, natural gas and petroleum 
  • Name methane as the main constituent of natural gas 
  • Describe petroleum as a mixture of hydrocarbons and its separation into useful fractions by fractional distillation 
  • Describe the properties of molecules within a fraction 
  • Name the uses of the fractions as: – refinery gas for bottled gas for heating and cooking – gasoline fraction for fuel (petrol) in cars – naphtha fraction for making chemicals – kerosene/paraffin fraction for jet fuel – diesel oil/gas oil for fuel in diesel engines – fuel oil fraction for fuel for ships and home heating systems – lubricating fraction for lubricants, waxes and polishes – bitumen for making roads

14.3 Homologous series

Core 

  • Describe the concept of homologous series as a ‘family’ of similar compounds with similar chemical properties due to the presence of the same functional group

Supplement 

  • Describe the general characteristics of a homologous series
  • Recall that the compounds in a homologous series have the same general formula 
  • Describe and identify structural isomerism

14.4 Alkanes

  • Core 

Describe the properties of alkanes (exemplified by methane) as being generally unreactive, except in terms of burning 

Describe the bonding in alkanes

Supplement

  • Describe substitution reactions of alkanes with chlorine

14.5 Alkenes

Core 

  • Describe the manufacture of alkenes and of hydrogen by cracking 
  • Distinguish between saturated and unsaturated hydrocarbons: – from molecular structures – by reaction with aqueous bromine
  • Describe the formation of poly(ethene) as an example of addition polymerisation of monomer units

Supplement 

  • Describe the properties of alkenes in terms of addition reactions with bromine, hydrogen and steam 14.6 Alcohols Core • Describe the manufacture of ethanol by fermentation and by the catalytic addition of steam to ethene • Describe the properties of ethanol in terms of burning • Name the uses of ethanol as a solvent and as a fuel Supplement • Outline the advantages and disadvantages of these two methods of manufacturing ethanol

14.7 Carboxylic acids

Core 

  • Describe the properties of aqueous ethanoic acid

Supplement 

  • Describe the formation of ethanoic acid by the oxidation of ethanol by fermentation and with acidified potassium manganate(VII) 
  • Describe ethanoic acid as a typical weak acid 
  • Describe the reaction of a carboxylic acid with an alcohol in the presence of a catalyst to give an ester

14.8 Polymers

14.8.1 Polymers

Core

  • Define polymers as large molecules built up from small units (monomers) Supplement • Understand that different polymers have different units and/or different linkages

14.8.2 Synthetic polymers

Core

  • Name some typical uses of plastics and of man-made fibres such as nylon and Terylene 
  • Describe the pollution problems caused by non-biodegradable plastics Supplement • Explain the differences between condensation and addition polymerisation 
  • Deduce the structure of the polymer product from a given alkene and vice versa
  • Describe the formation of nylon (a polyamide) and Terylene (a polyester) by condensation polymerisation, the structure of nylon 
  • Name proteins and carbohydrates as constituents of food Supplement • Describe proteins as possessing the same (amide) linkages as nylon but with different units 
  • Describe the structure of proteins
  • Describe the hydrolysis of proteins to amino acids. (Structures and names are not required.)
  • Describe complex carbohydrates in terms of a large number of sugar units,
  • Describe the hydrolysis of complex carbohydrates (e.g. starch), by acids or enzymes to give simple sugars 
  • Describe the fermentation of simple sugars to produce ethanol (and carbon dioxide). (Candidates will not be expected to give the molecular formulae of sugars.) 
  • Describe, in outline, the usefulness of chromatography in separating and identifying the products of hydrolysis of carbohydrates and proteins

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