alkanes (organic chem) Flashcards
hydrocarbons, fractional distillation of crude oil, uses of alkanes,cracking, combustion
define βalkanesβ
saturated hydrocarbons
define βpetroleum fractionβ
mixture of hydrocarbons with similar chain length & b.p range
gen. formula of alkanes
CnH(2n+2)
reactivity of alkanes
(and why?)
unreactive apart from combustion β> strong, non-polar C-C & C-H bonds
process of fractional distillation of crude oil
> the petroleum fractions condense at diff. heights
the temp. of the column decreases upwards
smaller molecules condense at top β> lower temp = lower b.p β> smaller size β> smaller VDWs
larger molecules condense at bottom β> higher temp = higher b.p β> larger size β> larger VDws
smaller molecule characteristics
- lighter colour
- very flammable
- low viscosity
larger molecule characteristics
- darker colour
- less flammable
- high viscosity
vacuum distillation
- heavy residue from fractionating column distilled under vac.
- lowering the pressure over a liquid = lower b.p
why might vacuum distillation be used?
- allows heavier fractions to be further seperated
- no need for high temps β> could break them down
define βcrackingβ
conversion of long hydrocarbons to smaller, more useful hydrocarbon molecules by breakage of C-C bonds
high Mr alkanes β>
smaller Mr alkanes + alkenes + (hydrogen)
name a solid material made from alkanes
polymer
why does cracking req. high temps?
involves splitting of strong cov. bonds (C-C)
list the economic reasons for cracking
- petroleum fractions with shorter C chains (eg. petrol) are higher in demand
- products of cracking = more valuable than starting materials
conditions for thermal cracking
- high pressure (7000kPa)
- high temp. (400-900 degrees)
products of thermal cracking
- mostly alkenes
- sometimes prod. hydrogen
process of thermal cracking
- proceeds via free radical mechanism
- 1st step is homolytic fission of C-C bond
conditions for catalytic cracking
- slight pressure
- high temp (450 degrees)
- zeolite catalyst
products of catalytic cracking
- branched and cyclic alkanes
- aromatic hydrocarbons
why is catalytic cracking used?
- branched/cyclic hydrocarbons burn more smoothly than unbranched ones β> used to give fuels higher octane no.
- cheaper than t. cracking β> uses less energy β> lower temp n pressure
why are alkanes used as fuels?
- they burn readily in presence of oxygen
- this combustion of alkanes = highly exo.
- can be used as fuels (fuels release heat energy when burnt)
complete combustion
- fuel + O2 β> CO2 + H2O
- excess O2
incomplete combustion
-
fuel + O2 β> C or CO + steam
β> CO = colourless, odourless, toxic gas which bonds to haemoglobin
β> C = causes global dimming, respiratory issues - insufficient O2
types of pollution from combustion
- sulphur impurities
- nitrogen oxides
- greenhouse gases