Wednesday, 3 June 2015

2.10.2a: demonstrate an understanding of the nomenclature and corresponding structural, displayed and skeletal formulae for halogenoalkanes, including the distinction between primary, secondary and tertiary structures

Halogenoalkanes:
  • general formula: CnH2n+X (where X is a halogen)
  • polar molecules with a polar C-X bond (different electronegativities)
    • electronegativity and polarity decreases down the group
  • solubility:
    • only sparingly soluble in water, at best, because they are not polar enough to break the hydrogen bonds between water molecules
    • much more soluble in a water/ethanol mixture because they are able to bond with the ethanol chains
  • flammability:
    • decreases as the number of halogen atoms increases
  • density:
    • increases with the number and mass of halogen atoms
  • boiling points:
    • the longer the chain, the higher the boiling point, as van der Waals forces get stronger
Primary, secondary, and tertiary halogenoalkanes:

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