HALOGENALKANES

Cards (76)

  • What is a Halo alkane?
    An alkane with a halogen attached
  • What is an example of a Halo alkane derived from methane?
    Chloromethane
  • How is a Halo alkane formed from an alkane?
    By replacing a hydrogen with a halogen
  • What is the process used to synthesize Halo alkanes?
    Free radical substitution
  • What are the three steps of Halo alkane synthesis?
    1. Initiation step
    2. Propagation step (two stages)
    3. Termination step
  • What is the first step in Halo alkane synthesis?
    Initiation step
  • What occurs during the initiation step?
    A halogen molecule breaks down into free radicals
  • What is the representation of a free radical?
    A single unpaired electron denoted by a dot
  • What causes the halogen bond to break in the initiation step?
    UV light
  • What is the result of the initiation step when chlorine is involved?
    Two chlorine free radicals are produced
  • What happens during the first stage of the propagation step?
    A methane molecule reacts with a chlorine free radical
  • What is formed when methane reacts with a chlorine free radical?
    Chloromethane and hydrogen chloride
  • What is the role of the chlorine free radical in the propagation step?
    It acts as a catalyst
  • How does the propagation step contribute to Halo alkane synthesis?
    It produces the Halo alkane through substitution
  • What is the final step of Halo alkane synthesis?
    Termination step
  • What occurs during the termination step?
    Two radicals combine to form a non-radical
  • What is an example of a termination step involving chlorine radicals?
    Two chlorine radicals forming chlorine gas
  • What is the significance of CFCs in relation to ozone depletion?
    CFCs release chlorine radicals that attack ozone
  • Why were CFCs widely used before their ban?
    They were effective solvents and refrigerants
  • What happens to CFCs when they reach the atmosphere?
    They break down under UV light
  • Why is the carbon-chlorine bond more likely to break than the carbon-fluorine bond?
    The carbon-chlorine bond is weaker
  • What is the consequence of ozone depletion?
    Increased UV radiation exposure
  • What is the chemical formula for chlorofluorocarbons (CFCs)?
    Examples include CCl2F2 and CHClF2
  • What is the role of ozone in the atmosphere?
    It filters UV radiation from the Sun
  • What is the relationship between CFCs and skin cancer?
    Increased CFCs lead to more UV exposure
  • What is the focus of this lesson?
    Nucleophilic substitution
  • What is nucleophilic substitution classified under in AQA Chemistry?
    It is one of three mechanisms
  • In which section of AQA Chemistry Unit 2 is nucleophilic substitution found?
    Haloalkanes
  • What does the term 'nucleophile' break down into?
    Nuclear and file
  • What does 'nucleo' relate to in the context of nucleophiles?
    It relates to positivity, like a nucleus
  • What does the term 'substitution' mean in nucleophilic substitution?
    It means to swap
  • What is the significance of bromine in bromoethane?
    Bromine allows nucleophilic attack
  • Why does the carbon-bromine bond allow for nucleophilic substitution?
    Bromine is more electronegative than carbon
  • What does the term 'Delta' imply in the context of charge?
    It indicates a difference in charge
  • What is the definition of a nucleophile?
    An electron pair donor
  • What does the double-headed arrow signify in nucleophilic substitution?
    Movement of a pair of electrons
  • What happens to the carbon-bromine bond during nucleophilic substitution?
    Electrons move from the bond to bromine
  • What are the three nucleophiles expected to be known in this unit?
    Hydroxide ion, cyanide ion, ammonia
  • How does the hydroxide ion act as a nucleophile?
    It has a lone pair of electrons
  • What product is formed when hydroxide ion attacks bromoethane?
    Ethanol