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Alkanes and Alkenes
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Hydrocarbon molecules vary in
size
, affecting their
properties
and how they can be used as
fuels
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The larger the hydrocarbon:
the more
viscous
it is (flows less easily)
the
higher
its boiling point
the
less
volatile it is and the less easily it
ignites
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Each fraction contains
hydrocarbon molecules
with a similar number of
carbon atoms
and similar
boiling points
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Most
hydrocarbons
obtained from
fractional
distillation are
alkanes
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During
fractional
distillation, the crude oil is
heated
until it
evaporates
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The
vapour
moves up the
fractionating column
, with the top being much
colder
than the bottom
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Shorter
hydrocarbon molecules reach the top of the column before
condensing
and are collected
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Longer
hydrocarbon molecules
condense
at
higher
temperatures and are collected
lower
down the column
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Hydrogen
can be added to
alkenes
to produce
alkanes
, using a
nickel catalyst
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Example:
propene
+
hydrogen
->
propane
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This is an
addition
reaction
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Ethanol
can be produced by reacting
ethene
with
steam
in the presence of
phosphoric acid catalyst
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Example:
ethene
+
steam
->
ethanol
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Bromine
Water test
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Alkenes react with
bromine water
, turning it from
orange
to
colourless
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This reaction can be used to
differentiate
between
alkanes
and
alkenes
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Example:
ethene
(
colourless
) +
bromine water
(
orange brown
) ->
colourless
solution
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Example:
ethane
(
colourless
) +
bromine water
(
orange brown
) ->
remains orange brown solution
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Cracking
is the process of breaking
longer-chain
hydrocarbons into
shorter
, more
useful
hydrocarbons
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During
catalytic
cracking:
Hydrocarbons
are
heated
until they
vaporise
The
vapour
is passed over a hot
catalyst
A
thermal decomposition reaction
takes place
The products include
alkanes
and
alkenes
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During
steam
cracking,
hydrocarbons
are mixed with
steam
and
heated
to a
high
temperature
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Products of cracking
are useful as
fuels
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There is a
high
demand for fuels with
small
chains of
carbon
atoms because they are
easy
to
ignite
and have
low
boiling points
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