Alkanes ✂️

Cards (14)

  • what is the general formula of an alkane?
    general formula of CnH2n+2
  • what type of bonding does an alkane have?
    saturated- only contain single covalent bonds
    each carbon atom has four sigma bonds
    sigma bond- overlap of two orbitals, one from each bonding atom
    • each orbital has one electron so therefore each sigma bond has two electrons shared between the bonding atoms
  • what is the bond angle of an alkane?
    • has 4 sigma bonds= repulsion causes a bond angle of 109.5 around eavh carbon
  • How do boiling points change in alkanes?
    More carbons in alkane= higher boiling point
    • longer chain length =more London forces more energy required to break forces
    • longer chain length= larger surface area and more surface contact therefore more London forces
  • How does branching affect the boiling point?
    • branched isomers have lower boiling points
    • fewer points of contact between molecules of branched alkanes = less London forces= less energy required
    • shape also means that the packing of molecules is not tight and the molecules wont be as close together = more further= decreases intermolecular forces= less energy required
  • Why are alkanes not that reactive?
    C-C bonds are non polar and the electronegativity between Cand H is so similar they can be considered non polar too and therefore find it difficult to attract molecules
    C-H and C-C sigma bonds are strong
  • why are alkanes used as fuels?
    because they react with a plentiful supply of oxygen in a combustion reaction
    producing carbon dioxide and water
  • What is the incomplete combustion of alkanes and what does it produce?
    When there is a limited supply of oxygen and carbon monoxide or just carbon is formed alongside water
  • how do alkanes react with halogens and what conditions are needed?
    an alkane reacting with a halogen requires UV radiation from the sunlight to provide the initial energy needed for the reaction to occur
    the reaction is a substitution react where the hydrogen atom replaces the bromine atom
  • what is the mechanism for an alkane reacting with a halogen called and what are the three steps?
    • radical substitution
    • initiation, propagation and termination
  • what happens in initiation stage of bromination of an alkane?
    • covalent bond between bromine molecules broken by homolytic fission
    • both atoms take one radical
    • must have UV light present
    • radical is very reactive
  • what happens in the propagation stage of bromination of an alkane?
    • chain reaction so two steps occur
    • step 1= Br radical reacts with the C-H bond, forming a CH3 radical, and a molecule of hydrogen bromide (HBr)
    • step 2= the methyl radical reacts with another bromine molecule to form CH3Br and a Br radical
    • in theory these two steps can occur till all reactant is used up but in practise the step is terminated when the two radicals collide
  • What happens in the termination stage of bromination of an alkane?
    • two radicals collide and there are more than one possibility of collisions so there are more than one termination steps
  • what are the potential weaknesses of using radical substitution to make haloalkanes?
    • the bromine radical can collide with the bromoethane molecule for example to make dibromoethane, this substitution can occur until all hydrogen atoms have been substituted
    • If carbon chain is longer than the substitution of a hydrogen atom by a bromine atom can occur in different positions leading to different isomers