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Organic Chemistry
Cracking + Alkenes
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Cracking
Hydrocarbons
can be broken down (cracked) to produce
smaller
, more
useful
molecules.
Products of cracking (long-chain hydrocarbons)
useful as
fuels
polymers e.g
plastics
Cracking
Thermal
decomposition
Two types of cracking
Catalytic
cracking
Steam
cracking
Catalytic cracking
heat
the long-chain hydrocarbon to
vaporise
/
evaporate
them
passed over a hot, powdered
catalyst
crack on the surface on the specs of the
catalyst
Steam cracking
heat
the long-chain hydrocarbon to
vaporise
/
evaporate
them
mixed with
steam
and
heated
to a very
high
temperature
lead to the thermal
decomposition
of long-chain hydrocarbon molecules to form
smaller
one
Give two conditions used to crack large alkane molecules.
High
temperatures
Catalyst
OR
steam
Similarity between Catalytic cracking and Steam cracking
heat
long-chain hydrocarbons to
vaporise
/
evaporate
them
Products of cracking 2
alkanes
alkenes
Cracking of decane
decane =
ethene
+
octane
Economic reasons for cracking
There is a
high
demand for fuels with
small
molecules
Alkenes
unsaturated hydrocarbons
homologous
series
General formula of alkenes
CnH2n
Alkenes are
hydrocarbons
contain
hydrogen
and
carbon
atoms only
Reactivity : alkenes
more reactive
than alkanes
Bonds in alkenes
form a single,
double carbon-carbon
bond
unsaturated
Carbon bonds in alkenes
carbon atoms always
4
bonds by
HYDROGEN
atoms make only
one
Uses of alkenes
produce
polymers
e.g ethene =
plastics
starting
materials for the production of other
chemicals
Why are alkenes more reactive than alkanes?
double
carbon-carbon bond can open up to become a
single
bond
this allows the
two
carbon atoms to
bond
to other atoms
First four alkenes
ethene
propene
butene
pentene
How do you know C5H10 is an alkene?
matches the
general
formula of an alkene :
CnH2n
Alkenes
+
bromine water
When
alkenes
react with
bromine water
, the
colour
changes from
orange
to
colourless
Alkanes + bromine water
When
alkanes
react with
bromine
water,
no reaction
occurs and solution remains
orange
Pentene is useful because many pentene molecules can
join
together
to form .................................................. .
poly
(pentene)
Complete Combustion of alkenes
plentiful
supply of
oxygen
combust
completely
produce
carbon dioxide
+
water
(vapour)
Incomplete combustion
limited
supply of
oxygen
also produces, carbon
monoxide
+
carbon
(soot)
Complete combustion v Incomplete combustion
less
energy is released by
incomplete
combustion
long chain hydrocarbon -->
long chain hydrocarbon -->
shorter
chain molecule
alkane
+
alkene
Alkenes : functional group
contain a
double
carbon-carbon
functional
group
Why are alkenes considered part of a homologous series?
all contain
double
carbon-carbon functional group
all react in
similar
ways
Why are alkene molecules unsaturated?
contain
two
fewer
hydrogen
carbon atoms than the alkane with the
same
number of carbon atoms
Flame in incomplete combustion of alkenes
burn
with a
smoky yellow
flame
Why are
alkenes
useful?
reactive
Feedstock
Solvents
Detergents
Fuels
petrol
kerosene
Catalyst that can be used for catalytic cracking
aluminium oxide
Suggest how the use of a suspension of limestone decreases one of the environmental impacts that the waste gases would cause
acid rain
is caused by
sulphur dioxide
global warming
is caused by
carbon dioxide
carbon dioxide
dissolve in suspension by
limestone