12.1 -12.2 Flashcards
What are alkanes
- saturated hydrocarbons
What does a compound being saturated mean
- all the carbon bonds are bonded 4 times
What is the general formula of alkanes
- CnH2n+2
What is the shape and bond angle of alkanes
- tetrahedral (109.5)
Why do alkanes have a specific shape with specific angle
- because the bond repel each other equally
If a molecule has no branching what does this mean
- molecules can pack together closely leading to more surface contact
Why is the boiling point for longer straight chain high
- they have more London forces so more energy is needed to overcome these forces so a high boiling point
What is the boiling point for branched hydrocarbons
- they can’t pack closely together which weakens the London forces between the chain so they have a lower boiling point
What do alkanes form when they are completely combusted
- CO2 and H2O
What are alkanes good as
- fuels as most burn readily to produce large amounts of energy
- used to power vehicles
- used in most of Britain’s electricity
Using combustion equations:
15cm^3 of hydrocarbon ‘A’ burns completely in 120cm^3 of oxygen. 75cm^3 of carbon dioxide is produced what is the molecular formula of hydrocarbon A?
FORMULA: C5H12
1) use info to write a volume ratio equation
2) simplify ratio
3) 8 moles of O2 reacts to form 5 moles of CO2 and the ‘n’ moles of H2O. Any oxygen that isn’t in CO2 must be in H2O
4) combustion equation is
5) to identify ‘A’- all carbon in ‘A’ make CO2 and the number of hydrogens in ‘A’ must be 12 (we have 6H2O)
What is incomplete combustion
- alkanes burning with a limited oxygen supply
What is produced in incomplete combustion
- carbon monoxide(CO) and carbon(soot)
What problems does carbon monoxide cause
- poisonous as it bonds to haemoglobin in the blood preventing oxygen from binding
What problems does soot cause
- breathing problems
What reaction do alkanes undergo
- free radical reactions
What type of bond fission happens in free radical substitution reactions
- homolytic fission
What are the three steps of free radical substitution reactions
1) Initiation
2) Propagation
3) Termination
What is the catalyst in free radical substitution
- UV light
What happens in initiation
- radicals are produced by breaking a covalent bond forming two radical using UV light
What happens in propagation
- radicals react with non-radicals to form radicals and non radicals
What happens in termination
- 2 radicals react and form a non-radical molecules
- ends the chain reaction
Write the free radical substitution reaction for this reaction:
CH4 + Cl2 —> CH3Cl + HCl
Initiation:
UV
Cl2——> Cl . + Cl .
Propagation:
1) Cl . + CH4 —-> . CH3 + HCl
2) . CH3 + Cl2 —> CH3Cl + Cl .
Termination:
1) Cl . + Cl . —> Cl2
2) . CH3 + . CH3 —> C2H6
3) . CH3 + . Cl —> CH3Cl
What are usually the products of free radical substitution reaction
- normally a mixture of product
- so it has a low percentage yield
What is required to get your desired product in free radical substitution
- further substitution