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What is an
ACID and
Base?
Classifications
Classifications
Bronsted-lowry Study Quiz
C. pH scale → 0 -14 →
Indicates concentration of
hydronium ions
• 0-6 = acid → closer to 0 is
more acidic
• 8-14 = base → closer to 14 is
more basic
• 7 = neutral → H3O+
concentration = OH-
concentrations
Review
How acidic or basic is it?
D. Each pH unit = a power of ten
• Example: pH 3 is 100 times more acidic than pH 5
Review Review
• Strong Acid: An acid that has a very low pH (0-4).
Introduction
It is the measure of the change in concentration of the reactants or the change in concentration of
the products per unit time.
Rates of Reaction
Chemical reactions
will only occur when
the reacting particles
collide with each
other with sufficient
energy so they react.
Rates of Reaction
Temperature
Temperature
Pressure
(of gases)
Temperature
Pressure
(of gases)
Concentration
Temperature
Pressure
(of gases)
Pressure
Catalysts
(of gases)
Kinetic
what?
The ACTIVATION
ENERGY is the relatively
small amount of energy
needed to start a
chemical reaction
Activation energy
Activation energy
reactants
Used to break
apart the old
bonds
Increasing energy
products
Time
Activation energy
Activation energy
reactants
using a catalyst.
Increasing energy
the reaction – this
makes the reaction
go faster.
products
Time
Activation Energy Formula
K = Ae-Ea/RT
• K = Rate Constant
• A = Arrhenius Constant
• Ea = Activation Energy
• R = Gas constant = 8.34J/K/mol
Activation Energy Formula
Kinetic theory
is all about the
random
movement of
particles
Kinetic theory assumes
that particles are in
constant random motion
Kinetic theory
is all about the
!
random
movement of
particles
!
Kinetic theory is all about
the random movement of
particles
Do you remember
the five factors
that can affect the
rate of chemical
reactions?
Rates of Reaction
Rates of Reaction
Low temperature
HEAT
High temperature
Cold conditions, When heated,
particles have little particles have more
energy, move slowly energy, move faster,
and collide collide frequently
infrequently and and more
less successfully successfully
Rates of Reaction
1. Temperature of the Reactants
Low temperature
HEAT
High temperature
Cold conditions, When heated,
particles have little particles have more
energy, move slowly energy, move faster,
and collide collide frequently
infrequently and and more
less successfully successfully
Rates of Reaction
2. Concentration of the Dissolved Reactants
Rates of Reaction
2. Concentration of the Dissolved
Reactants
Low concentration
High concentration
Particles are spread Particles are
out and will collide crowded close
with each other less together, so collide
often, with fewer more often, with
successful collisions more successful
collisions
Rates of Reaction
2. Concentration of the Dissolved
Reactants
Low concentration
High concentration
Particles are spread Particles are
out and will collide crowded close
with each other less together, so collide
often, with fewer more often, with
successful collisions more successful
collisions
Rates of Reaction
3. Pressure (in gases)
Rates of Reaction
3. Pressure (in gases)
Low pressure
Low pressure
High pressure
Particles are spread Particles are pushed
out and will collide closer together, they
with each other less collide more
often, with fewer frequently, with
successful collisions more successful
collisions
Rates of Reaction
3. Pressure (in gases)
Low pressure
High pressure
Particles are spread Particles are pushed
out and will collide closer together,
with each other less they collide more
often, with fewer frequently, with
successful collisions more successful
collisions
Rates of Reaction
4. Surface area of solid reactants
Rates of Reaction
4. Surface area of solid reactants
Positive Catalysts
A catalyst that helps to increase
the rate of reaction or which
support the reaction to carry out
quickly is called a positive
catalyst. Such catalyst decreases
activation energy by accepting a
smaller path, so the rate of
reaction is increased.
Rates of Reaction
Types of Catalysts
1. Surface
area
Boiling tube
1. Surface
area
Boiling tube
Boiling tube
2.
Concentration
View from
Volume of sodium Volume of
above
thiosulphate (cm3) water (cm3)
10 40
10cm3 sodium
thiosulphate +
20 30
40cm3 water +
10cm3 30 20
hydrochloric acid
40 10
X 50 0
Rate of reaction experiments
2.
Concentration
10 40 98
10cm3 sodium
thiosulphate +
20 30 64
40cm3 water +
10cm3 30 20 31
hydrochloric acid
40 10 16
50 0 8
Rate of reaction experiments
Volume of thiosulphate
View from Time for cross
Volume of sodium Volume of
above to disappear
thiosulphate (cm3) water (cm3) (secs)
10 40 98
10cm3 sodium
thiosulphate +
20 30 64
40cm3 water +
10cm3 30 20 31
hydrochloric acid
40 10 16
50 0 8
Rate of reaction experiments
As the concentration of sodium
disappear
2.
Concentration
time taken decreases – the rate
of reaction gets faster.
Volume of thiosulphate
View from Time for cross
Volume of sodium Volume of
above to disappear
thiosulphate (cm3) water (cm3) (secs)
10 40 98
10cm3 sodium
thiosulphate +
20 30 64
40cm3 water +
10cm3 30 20 31
hydrochloric acid
40 10 16
50 0 8
Rate of reaction experiments
Temperature Reaction time (secs) Average
of reaction reaction time
mixture (oC) Experiment 1 Experiment 2 Experiment 3 (secs)
3.
Temperature 40 24 25 25 25
50 22 20 20 21
60 17 16 16 16
70 12 11 11 11
80 7 7 8 7
Rate of reaction experiments
Temperature Reaction time (secs) Average
of reaction reaction time
mixture (oC) Experiment 1 Experiment 2 Experiment 3 (secs)
3.
Temperature 40 24 25 25 25
50 22 20 20 21
60 17 16 16 16
70 12 11 11 11
80 7 7 8 7
Rate of reaction experiments
Temperature Reaction time (secs) Average
of reaction reaction time
mixture (oC) Experiment 1 Experiment 2 Experiment 3 (secs)
3.
Temperature 40 24 25 25 25
50 22 20 20 21
60 17 16 16 16
70 12 11 11 11
80 7 7 8 7
As the temperature
increases so the time
taken for the cross
to disappear
decreases – the
reaction gets faster.
Rate of reaction experiments
4.
Catalysts
Decomposition of hydrogen peroxide
2H2O2 → 2H2O + O2
produced.
Manganese oxide
catalyst
Rate of reaction experiments
4.
Catalysts
Decomposition of hydrogen peroxide
2H2O2 → 2H2O + O2
20
0
Manganese oxide 0 10 20 30 40 50 60 70 80 90 100
catalyst Time (secs)
Rate of reaction experiments
4.
Catalysts
Decomposition of hydrogen peroxide
2H2O2 → 2H2O + O2
2H2O2 → 2H2O + O2
plus
• particles must approach each other in a certain relative way -
STERIC EFFECT
COLLISION THEORY
Collision theory states that...
• particles must COLLIDE before a reaction can take place
• not all collisions lead to a reaction
• reactants must possess at least a minimum amount of energy – ACTIVATION ENERGY
plus
• particles must approach each other in a certain relative way - STERIC EFFECT
more frequent collisions increase particle speed or have more particles present
more successful collisions give particles more energy or lower the activation energy
INCREASING THE RATE
The following methods may be used to increase the
rate of a chemical reaction
• INCREASE TEMPERATURE
• SHINE LIGHT
• ADD A CATALYST
+
In many organic reactions there are two liquid layers, one aqueous, the other non-
aqueous. Shaking the mixture increases the reaction rate as an emulsion is often
formed and the area of the boundary layers is increased giving more collisions.
1
1
CUT THE SHAPE 1
1
INTO SMALLER 1
PIECES
3
3
ENERGY CHANGES
DURING A REACTION
According to KINETIC THEORY, all particles must have energy; the greater their
temperature, the more energy they possess. The greater their KINETIC ENERGY the faster
they travel.
ZARTMANN heated tin in an oven and directed the gaseous atoms at a rotating disc with a
slit in it. Any atoms which went through the slit hit the second disc and solidified on it.
Zartmann found that the deposit was spread out and was not the same thickness throughout.
This proved that there was a spread of velocities and the distribution was uneven.
ZARTMANN’S
EXPERIMENT
INCREASING TEMPERATURE
MAXWELL-BOLTZMANN
DISTRIBUTION OF
MOLECULAR ENERGY
MOLECULAR ENERGY
Experiments showed that, due to the many collisions taking place between
molecules, there is a spread of molecular energies and velocities.
MAXWELL-BOLTZMANN
DISTRIBUTION OF
MOLECULAR ENERGY
A PARTICULAR ENERGY
T2
TEMPERATURE
T2 > T1
MOLECULAR ENERGY
T3 MAXWELL-BOLTZMANN
DISTRIBUTION OF
MOLECULAR ENERGY
A PARTICULAR ENERGY
TEMPERATURE
T1 > T3
MOLECULAR ENERGY
T3 MAXWELL-BOLTZMANN
DISTRIBUTION OF
MOLECULAR ENERGY
A PARTICULAR ENERGY
T2
TEMPERATURE
T2 > T1 > T3
MOLECULAR ENERGY
REVIEW
no particles have zero energy/velocity
some particles have very low and some have very high energies/velocities
most have intermediate velocities
as the temperature increases the curves flatten, broaden and shift to higher energies
INCREASING TEMPERATURE
MAXWELL-BOLTZMANN
DISTRIBUTION OF
MOLECULAR ENERGY
MOLECULAR ENERGY
ACTIVATION ENERGY - Ea
The Activation Energy is the minimum energy required for a reaction to take place
The area under the curve beyond Ea corresponds to the number of molecules with
sufficient energy to overcome the energy barrier and react.
INCREASING TEMPERATURE
TEMPERATURE
MAXWELL-BOLTZMANN
T2 > T1 DISTRIBUTION OF
MOLECULAR ENERGY
A PARTICULAR ENERGY
T2
EXTRA
Ea MOLECULES WITH
SUFFICIENT
ENERGY TO
OVERCOME THE
ENERGY BARRIER
MOLECULAR ENERGY
Explanation
increasing the temperature gives more particles an energy greater than Ea
more reactants are able to overcome the energy barrier and form products
a small rise in temperature can lead to a large increase in rate
ADDING A CATALYST
• Catalysts provide an alternative reaction pathway with a lower Activation Energy (Ea)
• Decreasing the Activation Energy means that more particles will have sufficient
energy to overcome the energy barrier and react
MAXWELL-BOLTZMANN
DISTRIBUTION OF
MOLECULAR ENERGY
MOLECULAR ENERGY Ea
The area under the curve beyond Ea corresponds to the number of molecules with
sufficient energy to overcome the energy barrier and react.
If a catalyst is added, the Activation Energy is lowered - Ea will move to the left.
ADDING A CATALYST
MAXWELL-BOLTZMANN
DISTRIBUTION OF
MOLECULAR ENERGY
MOLECULAR ENERGY Ea
The area under the curve beyond Ea corresponds to the number of molecules with
sufficient energy to overcome the energy barrier and react.
Lowering the Activation Energy, Ea, results in a greater area under the curve after Ea
showing that more molecules have energies in excess of the Activation Energy
CATALYSTS - A REVIEW
allow reactions to take place at lower temperatures SAVE ENERGY (lower Ea)
REDUCE CO2 OUTPUT
allow reactions to take place at lower temperatures SAVE ENERGY (lower Ea)
REDUCE CO2 OUTPUT
allow reactions to take place at lower temperatures SAVE ENERGY (lower Ea)
REDUCE CO2 OUTPUT
allow reactions to take place at lower temperatures SAVE ENERGY (lower Ea)
REDUCE CO2 OUTPUT
• shining a suitable light source onto some reactants increases the rate of reaction
• the light - often U.V. - provides energy to break bonds and initiate a reaction
• the greater the intensity of the light, the greater the effect
The more particles there are in a given volume, the greater the pressure
The greater the pressure, the more frequent the collisions
The more frequent the collisions, the greater the chance of a reaction
INCREASING CONCENTRATION
Reactions are fastest at the start and get slower as the reactants concentration drops.
Reactants (A and B)
Concentration decreases with time
Product (C)
Concentration increases with time
CONCENTRATION
C
• the steeper the curve the faster the
rate of the reaction
e.g. Extracting a sample from the reaction mixture and analysing it by titration.
- this is often used if an acid is one of the reactants or products
More details of these and other methods can be found in suitable text-books.
MEASURING THE RATE
RATE How much concentration changes with time. It is the equivalent of velocity.
CONCENTRATION
y
gradient = y
x
TIME
• the rate of change of concentration is found from the slope (gradient) of the curve
• the slope at the start of the reaction will give the INITIAL RATE
• the slope gets less (showing the rate is slowing down) as the reaction proceeds
REVISION CHECK
What should you be able to do?