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 surfacearea and more surfacecontact 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 nonpolar and the electronegativity between Cand H is so similar they can be considered nonpolar 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 carbondioxide and water
What is the incomplete combustion of alkanes and what does it produce?
When there is a limited supply of oxygen and carbonmonoxide 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 UVradiation 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?
radicalsubstitution
initiation, propagation and termination
what happens in initiation stage of bromination of an alkane?
covalent bond between bromine molecules broken by homolyticfission
both atoms take one radical
must have UVlight 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 hydrogenbromide (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 differentpositions leading to different isomers