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Chemistry
Fuels, Alkanes and Alkenes
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Homologous series
A family of
organic
compounds with the same
functional
group and similar
chemical
properties
Functional group
An atom or a group of atoms that gives a
molecule
its characteristic
properties
Homologous series
Alkanes
Alkenes
Alcohols
Carboxylic acids
Homologous series and their functional groups
Alkanes
:
no
functional group
Alkenes
:
carbon-carbon
double
covalent
bond
Alcohols
:
hydroxyl
group
Carboxylic acids
:
carboxyl
group
General characteristics of a homologous series
Same
functional
group
Similar
chemical
properties
Different from the next member by
–CH2–
group
Gradual
change
in
physical
properties
Same
general
formula
Prepared using
similar
methods
Prefix
Shows the
number
of
carbon
atoms in each molecule
Suffix
Shows the
homologous series
that the compound
belongs
to
Suffixes and their corresponding homologous series
–ane
: alkane
–ene
: alkene
–ol
: alcohol
–oic
acid: carboxylic acid
Alkanes
Saturated hydrocarbons
that contain only
carbon–carbon single covalent
bonds
General molecular formula for
alkanes
CnH2n+2
where n = 1, 2,
3
etc.
Each member of the alkane homologous series differs from the next by a
–CH2–
unit
Unbranched alkanes
Methane:
CH4
Ethane:
C2H6
Propane:
C3H8
Physical properties of alkanes
Low
melting and boiling points
Insoluble
in water
Soluble
in organic solvents
Physical properties trends of alkanes
Melting
and
boiling
points
increase
down the homologous series
Alkanes are generally
unreactive
except in terms of
combustion
and
substitution
by
chlorine
Combustion of
alkanes
1.
Burn
in excess air to produce
carbon dioxide
and water vapour
2. Complete combustion produces
carbon dioxide
and
water
only
3. Incomplete combustion produces
carbon dioxide
, carbon monoxide, soot, and
water
Substitution reactions of alkanes
React with
halogens
in the presence of
UV
light
Alkenes
Unsaturated
hydrocarbons that contain
one
or more carbon–carbon double bonds
General
molecular formula
for
alkenes
CnH2n
where n =
2
, 3, 4, etc.
Unbranched alkenes
Ethene:
C2H4
Propene:
C3H6
Physical properties of alkenes
Low
melting and boiling points
Insoluble
in water
Soluble
in organic solvents
Combustion of alkenes
1. Burn in
excess
air to produce
carbon dioxide
and
water vapour
2.
Incomplete
combustion produces
carbon
dioxide
,
carbon
monoxide
,
water vapour
, and
carbon
Addition reactions of alkenes
Carbon–carbon double bonds
are
very
reactive
and undergo
addition
reactions readily
Addition reaction: Hydrogenation
1. Addition of
hydrogen
to
alkenes
to form
alkanes
2. Conditions:
High
temperature,
nickel
catalyst
Addition reaction:
Bromination
1. Addition of
bromine
to
alkenes
to form
bromoalkanes
2. Conditions:
Room
temperature and
pressure
Alkane does not
decolourise bromine
solution under
normal
conditions
Alkene
decolourises
reddish-brown
bromine
solution
Polyunsaturated
fat molecules
Contain
more
than
one
–C=C– bond in their molecules
Manufacture of
margarine
Reacting
unsaturated
vegetable oils with
hydrogen
in the presence of
nickel catalyst
at
high
temperature
and
pressure
Types of fats
Saturated
fats:
solids
at r.t.p.
Unsaturated
fats:
liquids
at r.t.p.
Examples of fats and oils
Fats:
butter,
margarine
Oils:
vegetable
oil,
olive
oil
Cracking
A process in which
larger
hydrocarbon
molecules
are
broken
into
smaller
hydrocarbon
molecules
How cracking is done
1. Using a
catalyst
at
high
temperature
2. Conditions:
Aluminium oxide
and
silicon
(
IV
)
oxide,
high
temperature,
pressure
of
1
atm
An
alkene
is
always
produced in
cracking
Organic Compounds
All
organic
compounds contain the
element carbon
Not all carbon-containing compounds are
organic
Non-organic carbon-containing compounds
Carbon dioxide
Carbon monoxide
Metal carbonates
Hydrocarbons
Organic compounds that contain only
hydrogen
and
carbon
Example of a
hydrocarbon
Crude Oil (
Petroleum
)
Crude oil consists mainly of
hydrocarbons
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