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07/09/13
C14 Organic ChemistryC14 Organic Chemistry
Syllabus statementsSyllabus statements
14.1 Fuels14.1 Fuels
1. Recall coal, natural gas and petroleum as fossil
fuels that produce carbon dioxide on combustion.
2. Understand the essential principle of
fractional distillation in terms of differing boiling
points (ranges) of fractions related to molecular
size and intermolecular attractive forces.
14.1 Fuels14.1 Fuels
3. Name methane as the main constituent of
natural gas.
4. Describe petroleum as a mixture of
hydrocarbons and its separation into useful
fractions by fractional distillation.
14.1 Fuels14.1 Fuels
5. State the use of:
• refinery gas for bottled gas for heating
and cooking,
• gasoline fraction for fuel (petrol) in cars,
• diesel oil / gas oil for fuel in diesel engines.
14.2 Intro to organic cmpds14.2 Intro to organic cmpds
1. Identify and draw the structures of
methane, ethane, ethene and ethanol.
2. Describe the concept of homologous series
of alkanes and alkenes as families of
compounds with similar properties.
14.2 Intro to organic cmpds14.2 Intro to organic cmpds
3. State the type of compound present, given
a chemical name ending in -ane, -ene and -ol, or
a molecular structure.
4. Name, identify and draw the structures of
the unbranched alkanes and alkenes (not cis-
trans), containing up to four carbon atoms per
molecule.
14.3 Hydrocarbons14.3 Hydrocarbons
1. Describe the properties of alkanes
(exemplified by methane) as being generally
unreactive, except in terms of burning.
2. State that the products of complete
combustion of hydrocarbons, exemplified by
methane, are carbon dioxide and water.
14.3 Hydrocarbons14.3 Hydrocarbons
3. Name cracking as a reaction which produces
alkenes.
4. Describe the manufacture of alkenes by
cracking.
14.3 Hydrocarbons14.3 Hydrocarbons
5. Recognise saturated and unsaturated
hydrocarbons
• from molecular structures,
• by their reaction with aqueous bromine.
6. Describe the addition reactions of alkenes,
exemplified by ethene, with bromine, hydrogen
and steam
14.4 Alcohols14.4 Alcohols
1. State that ethanol may be formed by
reaction between ethene and steam.
2. Describe the formation of ethanol by the
catalytic addition of steam to ethene.
3. Describe the complete combustion reaction
of ethanol.
4. State the uses of ethanol as a solvent and
as a fuel.
14.5 Macromolecules14.5 Macromolecules
1. Describe macromolecules in terms of large
molecules built up from small units
(monomers), different macromolecules having
different units.
14.6 Synthetic polymers14.6 Synthetic polymers
1. Describe the formation of poly(ethene) as
an example of addition polymerisation of
monomer units.
2. Draw the structure of poly(ethene).
3. Describe the formation of a simple
condensation polymer exemplified by nylon,
the structure of nylon being represented as:
14.7 Natural macromolecules14.7 Natural macromolecules
1. Describe proteins as possessing the same
(amide) linkages as nylon but formed from the
linking of amino acids.
2. State that proteins can be hydrolysed to
amino acids under acid or alkaline conditions.
(Structures and names are not required.)

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C14 syllabus statements

  • 1. 07/09/13 C14 Organic ChemistryC14 Organic Chemistry Syllabus statementsSyllabus statements
  • 2. 14.1 Fuels14.1 Fuels 1. Recall coal, natural gas and petroleum as fossil fuels that produce carbon dioxide on combustion. 2. Understand the essential principle of fractional distillation in terms of differing boiling points (ranges) of fractions related to molecular size and intermolecular attractive forces.
  • 3. 14.1 Fuels14.1 Fuels 3. Name methane as the main constituent of natural gas. 4. Describe petroleum as a mixture of hydrocarbons and its separation into useful fractions by fractional distillation.
  • 4. 14.1 Fuels14.1 Fuels 5. State the use of: • refinery gas for bottled gas for heating and cooking, • gasoline fraction for fuel (petrol) in cars, • diesel oil / gas oil for fuel in diesel engines.
  • 5. 14.2 Intro to organic cmpds14.2 Intro to organic cmpds 1. Identify and draw the structures of methane, ethane, ethene and ethanol. 2. Describe the concept of homologous series of alkanes and alkenes as families of compounds with similar properties.
  • 6. 14.2 Intro to organic cmpds14.2 Intro to organic cmpds 3. State the type of compound present, given a chemical name ending in -ane, -ene and -ol, or a molecular structure. 4. Name, identify and draw the structures of the unbranched alkanes and alkenes (not cis- trans), containing up to four carbon atoms per molecule.
  • 7. 14.3 Hydrocarbons14.3 Hydrocarbons 1. Describe the properties of alkanes (exemplified by methane) as being generally unreactive, except in terms of burning. 2. State that the products of complete combustion of hydrocarbons, exemplified by methane, are carbon dioxide and water.
  • 8. 14.3 Hydrocarbons14.3 Hydrocarbons 3. Name cracking as a reaction which produces alkenes. 4. Describe the manufacture of alkenes by cracking.
  • 9. 14.3 Hydrocarbons14.3 Hydrocarbons 5. Recognise saturated and unsaturated hydrocarbons • from molecular structures, • by their reaction with aqueous bromine. 6. Describe the addition reactions of alkenes, exemplified by ethene, with bromine, hydrogen and steam
  • 10. 14.4 Alcohols14.4 Alcohols 1. State that ethanol may be formed by reaction between ethene and steam. 2. Describe the formation of ethanol by the catalytic addition of steam to ethene. 3. Describe the complete combustion reaction of ethanol. 4. State the uses of ethanol as a solvent and as a fuel.
  • 11. 14.5 Macromolecules14.5 Macromolecules 1. Describe macromolecules in terms of large molecules built up from small units (monomers), different macromolecules having different units.
  • 12. 14.6 Synthetic polymers14.6 Synthetic polymers 1. Describe the formation of poly(ethene) as an example of addition polymerisation of monomer units. 2. Draw the structure of poly(ethene). 3. Describe the formation of a simple condensation polymer exemplified by nylon, the structure of nylon being represented as:
  • 13. 14.7 Natural macromolecules14.7 Natural macromolecules 1. Describe proteins as possessing the same (amide) linkages as nylon but formed from the linking of amino acids. 2. State that proteins can be hydrolysed to amino acids under acid or alkaline conditions. (Structures and names are not required.)