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Rate of
reaction
How
quickly
a reaction happens
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Mean rate
The rate could be
changing
over the
time
you measure, but this is true for any measurement over time
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Experiment to measure rate of reaction
1. Reacting
hydrochloric
acid and
sodium thiosulfate
in a conical flask
2. Measuring the time until the solution becomes
cloudy
(increased
turbidity
)
3. Repeating at different
temperatures
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As temperature
increases
The time taken for the reaction
decreases
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Experiment to measure rate of reaction
1. Using a
gas syringe
to measure the
volume
of gas produced
2. Plotting a
graph
with quantity on y-axis and time on
x-axis
3. Drawing a
tangent
to find the
rate
at any point
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Factors that increase the rate of reaction
Increasing the
concentration
of reactants
Increasing the
pressure
of
gas
reactants
Increasing the
surface area
of
solid
reactants
Increasing
temperature
Adding a
catalyst
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Reversible reaction
Reactions where the
products
can return to the
original
reactants
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Equilibrium
The point where the rates of the
forward
and reverse reactions are equal, so there is
no
overall change
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Increasing pressure
Favours the
forward
reaction in a
reversible
reaction
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Increasing temperature
Favours the
endothermic
(reverse)
reaction
in a
reversible
reaction
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In a
reversible
reaction, if the forward reaction is exothermic, the reverse reaction must be endothermic, and vice versa
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Organic compounds
Compounds with a
carbon backbone
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Crude oil is the result of
plankton
being
buried
under water a long time ago
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Alkanes
Hydrocarbons
with
single-bonded
carbon atoms and hydrogen atoms
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Alkane names
Methane
Ethane
Propane
Butane
Pentane
Hexane
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Fractional distillation of crude oil
1.
Heating
to evaporate
2. Fractions
condense
at different heights in the
column
based on boiling points
3. Collecting the different
fractions
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Fractions from fractional distillation
LPG
(up to 4 carbons)
Petrol
Kerosene
Diesel oil
Heavy fuel oil
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Properties of fractions
Longer
fractions are
more viscous
Shorter
fractions are
more flammable
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Alkenes
Hydrocarbons
with a
carbon-carbon double
bond
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Unsaturated
Having a
carbon-carbon double
bond
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Testing for alkenes
1. Adding
bromine water
2.
Colourless
solution indicates the presence of an
alkene
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Cracking
Breaking down longer
alkanes
into shorter
alkanes
and alkenes
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Catalytic
cracking
Using a temperature of around
550°C
and a
zeolite
catalyst
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Steam cracking
Using a temperature over
800°C
with no
catalyst
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Alcohols
Organic compounds with an
-OH
functional group
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Reactions of alcohols
1.
Combustion
to form
carbon dioxide
and water
2. Reaction with
sodium
to form
sodium alkoxide
and hydrogen
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Carboxylic acids
Organic compounds with a
-COOH
functional group
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Addition polymerisation
Joining together
monomers
with a
double
bond
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Condensation polymerisation
Joining together
monomers
with two functional groups, producing
water
as a by-product
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Amino acids
Organic compounds with both an amino (
-NH2
) and a carboxyl (
-COOH
) group
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DNA
A large molecule that stores
genetic
code, made from two
polymers
that spiral around each other
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Starch
and
cellulose
Natural polymers
made from
glucose
monomers
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Melting point
and
boiling point
Tests to determine if a substance is
pure
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Formulation
A
mixture
designed for a specific purpose, with carefully controlled quantities of different
substances
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Chromatography
A technique for separating the components of a mixture
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Polymer
Molecules made from a large number of
monomers
joined together in a
chain
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Nucleotides
Four different
monomers
that make up
DNA
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Starch
Natural polymer where the monomer is
glucose
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Cellulose
Polymer made from
beta
glucose
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Amino acids
Monomers that make up
proteins
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