properties of alkenes

Cards (14)

  • pi bonds are formed by electrons in the adjacent p-orbitals overlapping above and below the carbon atoms
    -> this bond can only be made after a sigma bond has been formed
    • the pi bond holds the atoms in position by restricting rotation around the double bond so alkene molecules have a flat shape in the region of the double bonds - they are described as planar
  • the pi bond is the reactive part of the molecule because of the high electron density around it
  • alkene double bond shape and bond angle are trigonal planar and 120 degrees
  • alkenes are more reactive than alkanes due to high electron density of the double bond + the fact the pi bond is slightly easier to break
  • intermolecular forces of alkenes are only alkenes due to non-polar nature of the double bond
  • alkenes are insoluble in water because they have a double bond between carbon atoms which are non-polar bonds
  • types of isomers that can be formed using alkenes are :
    • E/Z isomers due to restricted rotation
    • Cis-trans isomers if two of the same substituents are attached to each carbon
  • most stable type of carbocation intermediate are alkyl groups as they have a positive inductive effect, so the most stable carbocation is the one bonded to the most other carbon atoms
    e.g. a tertiary carbocation
  • major products will be formed from tertiary carbocations (or the most stable available
  • Carbocation
    An electrically charged species that contains a positively charged carbon atom. Can be primary, secondary, or tertiary.
  • Stability
    The tendency of a carbocation to persist without undergoing further reaction. A more stable carbocation is less reactive and persists for a longer time.
  • Inductive effect
    A phenomenon in which the electrons in a bond are attracted towards a more electronegative atom. In carbocations, the positive charge on the carbon atom leads to a positive inductive effect, which stabilizes the carbocation.
  • Alkyl groups
    Have the most positive inductive effect among carbocations, since they have a greater number of carbon atoms bonded to the positively charged carbon. This makes them more stable.
  • Tertiary carbocation
    A carbocation with three other carbon atoms bonded to the positively charged carbon. It is more stable than secondary or primary carbocations due to the positive inductive effect.