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Transcript of rateofreaction-120105221844-phpapp01 (1)
Volume of
gas/ cm3
Time/ s
( 45 – 20 )
50
Rate of reaction =
Changes in amount of reactant/product
Time taken Increase in amount of product Decrease in amount of reactant
Concentration of
HCl / moldm-3
Mass of
ZnCO3 / g
Time/s Time/s
Volume of gas
CO2/cm3
Mass of
ZnCl2 / g
Time/s Time/s
ZnCO3(s) + 2HCl(aq) ZnCl2(aq) + CO2(g) + H2O(l)
MEASURING RATE OF REACTION
Average rate of reaction =
Change in selected quantity
Time taken
Instantaneous Rate Of
Reaction
= the gradient of the graph
at any given time.
The average rate of reaction =
for the whole reaction
= 0.444 cm3 s-1
40
90
Average rate of reaction in first
50 seconds
= Volume at 50 seconds
Time taken
= 30/50
=0.6 cm3 s-1
The average rate of reaction
between 50 and 90 seconds
= V at 50 s – V at 90 s
Time taken
= (40-30)/(90-50)
= 0.25 cm3 s-1
The rate of reaction at 50 second
= the gradient of tangent to the curve at the given
time
= ∆ y cm3
∆ x s
= 45 - 20
90 - 25
= 0.0345 cm3 s-1
- Plot a graph
- Draw a tangent
- Find the gradient
solution
Suitable measurable
changes:
� Colour
� Concentration
� Temperature
� Volume of gas
� Mass
� Precipitation
� Pressure
45
20
25 90
Volume of
gas/ cm3
Time/ s
( 45 – 20 )
50
( 90 – 25 )
40
30
25 90
18
High Rat e of reaction
-Fast reaction, short time
Low Rate of reaction
-Slower reaction, long time
Experiment I
(small chip)
Experiment II
(large chip)
CONCENTRATION
When concentration
of reactant increase
rate of reaction
increase
Gradient at t1 steeper > Gradient at t2
Rate of reaction t1 >Rate of reaction t2
Gradient in reaction I steeper > Gradient
in reaction II
Rate of reaction I >Rate of reaction II
Factors affecting rate of reaction
SIZE
When total surface
area larger, rate of
reaction increase
TEMPERATURE
When temperature
increases, rate of
reaction increase
PRESSURE
When pressure
increase rate of
reaction
increase
CATALYST
When positive
catalyst are used.
rate of reaction
Aim : To investigate the effect of the size of reactant
on the rate of reaction
Problem statement : How does the size of calcium
carbonate chips affect the rate of its reaction with
dilute hydrochloric acid?
Hypothesis : The rate of reaction between calsium
carbonate and hydrochloric acid is increases when
smaller size calcium carbonate used
Manipulated variable : The size of calcium carbonate
Responding variable : The rate of reaction
Fixed variables : Volume and concentration of HCl
Observable Change: Volume of gas CO2 in every 30 s
Time/s
• The rate of reaction in experiment II is higher than
experiment I because the gradient of the graph II is
greater than graph I throughout the reaction.
•••• The rate of reaction of the small calcium carbonate
chips is higher compared than large calcium
carbonate chip
• The maximum volume of carbon dioxide gas
collected for both experiments are equal because
the no. of mole of hydrochloric acid are the same
EFFECT OF THE SIZE OF REACTANT ON
RATE OF REACTION
Experiment I: 20 cm3 of 0.5 mol dm-3
hydrochloric acid + excess of CaCO3 SMALL
CHIPS
Experiment II: 20 cm3 of 0.5 mol dm-3
hydrochloric acid + excess of CaCO3 LARGE
CHIPS
Equation:
2CaCO3 + 2HCl CaCl2 + H2O + CO2
The number of mole of HCl in both experiments:
= MV/1000
= 22 x 0.5)/1000
=0.01 mol
CO2 gas
calcium
carbonate
hydrochloric acid
Water
CO2
Gas
Reaction has stopped
Volume of
carbon dioxide/ cm3
Observable Change: Yellow precipitate formed.
Aim : To investigate the effect concentration of sodium
thiosulphate on the rate of reaction
Problem statement : How does concentration of
sodium thiosulphate affect on the rate of reaction
Hypothesis : When concentration of sodium
thiosulphate increase, rate of reaction will increase.
Manipulated variable : concentration of sodium
thiosulphate
Responding variable : The rate of reaction
Fixed variables : Volume and concentration of HCl
� Concentration is inversely
proportional to time.
� When the concentration of
Na2S2O3 increases, a shorter
time is needed for marked
across to disappear.
� Concentration is directly
proportional to 1/time.
� [ 1/time shows the rate of
reaction ]
� When the concentration of
Na2S2O3 increases, the rate of
reaction is increase
Ionic Equation:
S2O3 2- + 2H+ S + SO2 + H2O
- The rate of reaction in exp I is
higher than exp II
- Exp I has higher concentration
than Exp II
- Gradient I is steeper than
graph II
- The maximum volume of
carbon dioxide gas collected
for both experiments are
equal
- no. of mole of hydrochloric
acid are the same
-
Exp I (high concentration)
Exp II (Low concentration)
Experiment 1 2 3 4 5
Volume of 0.2
moldm-3 Na2S2O3 ,
V1 cm3
50 40 30 20 10
Volume of distilled
water added/cm3 0.0 10 20 30 40
Volume of 1.0 mol
HCl acid added/cm3 5.0 5.0 5.0 5.0 5.0
Concentration of
Na2S2O3/moldm-3 0.2 0.16 0.12 0.08 0.04
Time taken/s 20 23 32 46 95
1/time , s-1 0.05 0.043 0.031 0.022 0.011
CONCENTRATION
‘X’
mark
Sodium thiosulphate
solution
+ Hydrochloric acid
Eye Experiment I: 50 cm3 of 0.2 mol dm-3 sodium
thiosulphate solution + 5 cm3 of 0.5 mol dm-3
hydrochloric acid
Experiment is repeated four times using 0.2 mol dm-3
sodium thiosulphate solution diluted with different
volume of distilled water
Equation:
Na2S2O3 + 2HCl 2NaCl + S + SO2 + H2O
Time /s
Concentration of
Na2S2O3 (mol dm-3) Experiment 1:
2.0 g Magnesium + 50 cm3 of
2.0 mol dm-3 hydrochloric
acid
Experiment II
2.0 g Magnesium + 50 cm3 of
1.0 mol dm-3 hydrochloric
acid
1/time (s-1)
Concentration of
Na2S2O3 (mol dm-3)
Time /s
Concentration of
Na2S2O3 (mol dm-3)
Volume of carbon dioxide/ cm3
Ionic Equation:
S2O3 2- + 2H+ S + SO2 + H2O
When the concentration
increase, Shorter time
is needed for mark ‘X’
disappear.
When temperature
increase, Shorter time
is needed for mark ‘X’
disappear.
Exp I
(high concentration)
Exp II
(low concentration)
Experiment 1 2 3 4
Temperature/oC 30 40 50 60
Volume of 0.2
moldm-3 Na2S2O3 , 50 40 30 20
Volume of distilled
water added/cm3 0.0 10 20 30
Volume of 1.0 mol
HCl acid added/cm3 5.0 5.0 5.0 5.0
Concentration of
Na2S2O3/moldm-3 0.2 0.16 0.12 0.08
Time taken/s 20 23 32 46
1/time , s-1 0.05 0.043 0.031 0.022
Equation:
Na2S2O3 + 2HCl 2NaCl + S + SO2 + H2O
CONCENTRATION TEMPERATURE
‘X’
mark
Sodium thiosulphate
solution
+ Hydrochloric acid
Eye
Observable changes:
Time required for mark
‘X’ disappear from view.
Concentration of
Na2S2O3 (mol dm-3)
Time /s
Concentration of Na2S2O3 (mol dm-3)
1/time (s-1)
concentration of Na2S2O3 increase
the rate of reaction increase
Time /s
Temperature
Na2S2O3 (mol dm-3)
Shows the rate of reaction
Temperature
Na2S2O3 (mol dm-3)
1/time (s-1)
Experiment 1:
2.0 g Magnesium + 50 cm3 of
1.0 mol dm-3 hydrochloric
acid at 25 oC
Experiment II
2.0 g Magnesium + 50 cm3 of
1.0 mol dm-3 hydrochloric
acid at 60 oC
Experiment is repeated four times using 0.2
mol dm-3 sodium thiosulphate solution diluted
with different volume of distilled water
‘X’
mark
Sodium thiosulphate
solution + Hydrochloric acid
Eye
Paper
sheet Paper
sheet
Experiment 1:
2.0 g Magnesium + 50 cm3 of 1.0 mol dm-3
hydrochloric acid
Experiment II
2.0 g Magnesium + 50 cm3 of 1.0 mol dm-3
sulphuric acid
Temperature of Na2S2O3 increase
the rate of reaction increase
Volume of H2
/ cm3
Time /s
Volume of H2
/ cm3
Time /s
Exp II (60 oC)
Exp I
(25 oC)
lower gradient
:. Lower rate
Steeper gradient
:. Higher rate
Decomposition
H2O2 2 H2O + O2
Exp I
(without
catalyst)
Lower gradient
:. Lower rate
Steeper gradient
:. Higher rate
PRESENCE OF CATALYST AMOUNT OF CATALYST
Observable changes:
The presence of oxygen
gas, tested with glowing
wooden splinter
� Manganese(IV) oxide act as catalyst
to increase rate of reaction
� Total volume for both exp I and II same
� Because the molarity and volume of
hydrogen peroxide in both reaction are
same
Experiment 1:
Decomposition of 50
cm3 of 1.0 mol dm-3
Hydrogen Peroxide
Experiment II
Decomposition of 50
cm3 of 1.0 mol dm-3
Hydrogen Peroxide +
1.0 g manganese (IV)
oxide
Problem statement : How does the presence of
catalyst affect the rate of composition of
hydrogen peroxide solution?
Hypothesis : Presence of catalyst increase the
rate of decomposition of hydrogen peroxide
Manipulated variable : Presence of catalyst
Responding variable : The rate of reaction
Fixed variables : temperature, volume and
concentration of hydrogen peroxide
Problem statement : How does the amount
of catalyst affect the rate of composition of
hydrogen peroxide solution?
Hypothesis : When amount of catalyst used
increase, the rate of decomposition of
hydrogen peroxide increase
Manipulated variable : Mass of catalyst
Responding variable : The rate of reaction
Fixed variables : temperature, volume and
concentration of hydrogen peroxide
Observable changes:
Volume of gas carbon
dioxide in every 30 s is
recorded
Experiment 1:
Decomposition of 50
cm3 of 1.0 mol dm-3
Hydrogen Peroxide +
0.5 g manganese (IV)
oxide
Experiment II
Decomposition of 50
cm3 of 1.0 mol dm-3
Hydrogen Peroxide +
1.0 g manganese (IV)
oxide
� When amount Manganese(IV)
oxide increase , rate of reaction
increase
� Total volume for both exp I and II
same
� Because the molarity and volume
of hydrogen peroxide in both
reaction are same
� Quantity of catalyst does not affect
the total volume of produced
Exp II
(1.0 g MnO2)
Exp I
(0.5 g MnO2)
Lower gradient
:. Lower rate
Steeper gradient
:. Higher rate
Properties of catalyst
� Need a small amount
� Specific in action
� Chemically unchanged
� Does not affect amount
product
� Increase rate of reaction
Volume of O2
/ cm3
Time /s
Volume of O2
/ cm3
Time /s
Exp II (with catalyst)
The collisions that lead to a chemical reaction are known as
effective collisions
.
Molecule ust collide
Right
orientation of collision
Achieved a minimun amoun of
energy (Ea)
The frequency of collision between particles
The smaller the size
of reactant, the
larger is the total
surface area
exposed to collision
The higher the
concentration of
reactants, the
higher is the
number of particles
in a unit volume.
The higher the
temperature,
higher is the
energy of reacting
particles.
reacting particles
move faster.
The frequency of effective collision between particles increases
The rate of reaction increases.
Explanation using Collision Theory
Cooking in a pressure cooker
� The high pressure in pressure cooker increases the boiling
point of water to a temperature above 100 °C.
� The kinetic energy of the particles in the food is higher
� Time taken for the food to be cooked is decrease
� Thus the food cooked faster at a higher temperature in a
pressure cooker.
SIZE
CONCENTRATION
TEMPERATUR
The collisions that lead to a chemical reaction are known as
Ea
”
Ea Achieved a
amoun of energy (Ea)
The Collision Theory
collision between particles increases.
The higher the
temperature, the
higher is the kinetic
energy of reacting
particles. The
reacting particles
move faster.
Catalyst provides
an alternative path
of reaction which
needs lower
activation energy
(Ea’)
collision between particles increases
increases.
Cooking of solid food in smaller size
� The total surface area on a smaller cut pieces of food is larger
� The food can absorbed more heat.
� The time taken for the food to be cooked is
Energy Profile Diagram And Activation Energy, E
Ea – The minimum energy the reactant
Ea’ – The lower activation energy in the presence
of a catalyst.
Energy
Explanation using Collision Theory
Storage of food in a refrigerator
� When the food kept in refrigerator, the food lasts longer
� The low temperature in the refrigerator slows down
activity of the bacteria.
� The bacteria produce less toxin ,
� the rate of decomposition of food becomes lower
in pressure cooker increases the boiling
higher.
in a
Reactant
reactants
products
Progress of reaction
Exothermic
reaction
CATALYST TEMPERATURE
Uses of
Catalyst in
Industrial
size
surface area on a smaller cut pieces of food is larger
heat.
me taken for the food to be cooked is shorter
Energy Profile Diagram And Activation Energy, Ea’:
The minimum energy the reactant
The lower activation energy in the presence
of a catalyst.
Progress of reaction
Endothermic
reaction
t in refrigerator, the food lasts longer
slows down the
lower
Energy
Product
Ea
Ea’
Reactant
Haber Process (NH3)
Iron, Fe
Ostwald process (HNO3)
Platinum, Pt
Contact process (H2SO4)
Vanadium (V) oxide,
V2O5
FACTOR EXPLANATION DIAGRAM
Size
Exp I:
2 g of Zinc chip + 50 cm3 1.0
mol dm-3 HCl
Exp II :
2 g of Zinc powder + 50 cm3 1.0
mol dm-3 HCl
Size of zinc in exp. II is smaller than exp I.
Total surface area exposed to collision in exp.
II is larger than exp. I
The frequency of collision between zinc and
hydrogen ion in exp II is higher
Frequency of effective collision between zinc
and hydrogen ion in exp II is higher
Rate of reaction in exp. II is higher
Concentration
Exp I: 2 g of Zinc powder + 50
cm3 0.5 mol dm-3 HCl
Exp II : 2 g of Zinc powder + 50
cm3 1.0 mol dm-3 HCl
Concentration of hydrochloric acid in exp. II is
higher than exp I
The number particles per unit volume in exp.
II is higher than exp. I
The frequency of collision between zinc and
hydrogen ion in exp II is higher
Frequency of effective collision between zinc
and hydrogen ion in exp II is higher
Rate of reaction in exp. II is higher
Concentration
Exp I: 2 g of Zinc powder + 50
cm3 1.0 mol dm-3 CH3COOH
Exp II : 2 g of Zinc powder + 50
cm3 1.0 mol dm-3 HCl
Exp III : 2 g of Zinc powder + 50
cm3 1.0 mol dm-3 H2SO4
Experiment I and II
Exp I use ethanoic acid (weak acid) and exp II use
hydrochloric acid (strong acid)
The number of hydrogen ions per unit volume
in exp. II is higher than exp. I
The frequency of collision between zinc and
hydrogen ion in exp II is higher
Frequency of effective collision between zinc
and hydrogen ion in exp II is higher
Rate of reaction in exp. II is higher
Experiment II and III
Exp III use sulphuric acid (diprotic acid) and exp
II use hydrochloric acid (monoprotic acid)
The number of hydrogen ions per unit volume
in exp. III is higher than exp. II
The frequency of collision between zinc and
hydrogen ion in exp II is higher
Frequency of effective collision between zinc
and hydrogen ion in exp II is higher
Rate of reaction in exp. II is higher
Volume of
H2/ cm3
Exp I
Exp II
Time/s
Volume of H2
/ cm3
Time /s
Exp II
Exp II
Volume of H2
/ cm3
Time /s
Exp III
Exp I
Exp II
Temperature
Exp I:
2 g of Zinc chip + 50 cm3 1.0
mol dm-3 HCl at 25 oC
Exp II :
2 g of Zinc powder + 50 cm3 1.0
mol dm-3 HCl at 40 oC
Temperature of exp. II is higher than exp I.
The kinetic energy of reactant in exp II is higher
than I
The frequency of collision
hydrogen ion in exp
Frequency of effective collision
and hydrogen ion in exp
Rate of reaction in exp. II is higher
Catalyst
Exp I:
2 g of Zinc powder + 50 cm3 0.5
mol dm-3 HCl
Exp II :
2 g of Zinc powder + 50 cm3 1.0
mol dm-3 HCl and 2cm3 of
copper (II) sulphate
Exp II use copper (II) sulphate act as catalyst
Catalyst provides an alternative path of reaction
which needs lo
The frequency of collision
hydrogen ion in exp
Frequency of effective collision
and hydrogen ion in exp
Rate of reaction in exp. II is higher
(with catalyst)
Temperature of exp. II is higher than exp I.
The kinetic energy of reactant in exp II is higher
frequency of collision between zinc and
hydrogen ion in exp II is higher
Frequency of effective collision between zinc
and hydrogen ion in exp II is higher
Rate of reaction in exp. II is higher
Exp II use copper (II) sulphate act as catalyst
Catalyst provides an alternative path of reaction
which needs lower activation energy (Ea’)
frequency of collision between zinc and
hydrogen ion in exp II is higher
Frequency of effective collision between zinc
and hydrogen ion in exp II is higher
Rate of reaction in exp. II is higher
Volume ofcarbon dioxide/ cm
Exp II
Volume of
/ cm3
Exp II (with catalyst)
Volume of carbon dioxide/ cm3
Exp I
Exp II
Time/s
Volume of H2
Time /s
Exp I
HAK MILIK SLM 2011