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U3 T1 Student Booklet 2

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ATAR Chemistry
Unit 3: Topic 1
Chemical Equilibrium Systems
3.1.1 Chemical Equilibrium
3.1.1.1 recognise that chemical systems may be open (allowing matter and energy to be exchanged with the
surroundings) or closed (allow energy, but not matter, to be exchanged with the surroundings)
3.1.1.2 understand that physical changes are usually reversible, whereas only some chemical reactions
are reversible
3.1.1.3 appreciate that observable changes in chemical reactions and physical changes can be described and explained
at an atomic and molecular level
3.1.1.4 symbolise equilibrium equations by using β‡Œ in balanced chemical equations
3.1.1.5 understand that, over time, physical changes and reversible chemical reactions reach a state of dynamic
equilibrium in a closed system, with the relative concentrations of products and reactants defining the position of
equilibrium
3.1.1.6 explain the reversibility of chemical reactions by considering the activation energies of the forward and reverse
reactions
3.1.1.7 analyse experimental data, including constructing and using appropriate graphical representations of relative
changes in the concentration of reactants and product against time, to identify the position of equilibrium.
3.1.2 Factors that affect equilibrium
3.1.2.1 explain and predict the effect of temperature change on chemical systems at equilibrium by considering the
enthalpy change for the forward and reverse reactions
3.1.2.2 explain the effect of changes of concentration and pressure on chemical systems at equilibrium by applying
collision theory to the forward and reverse reactions
3.1.2.3 apply Le Châtelier’s principle to predict the effect changes of temperature, concentration of chemicals, pressure
and the addition of a catalyst have on the position of equilibrium and on the value of the equilibrium constant.
3.1.3 Equilibrium constants
3.1.3.1 understand that equilibrium law expressions can be written for homogeneous and heterogeneous systems and
that the equilibrium constant (Kc), at any given temperature, indicates the relationship between product and reactant
concentrations at equilibrium
3.1.3.2 deduce the equilibrium law expression from the equation for a homogeneous reaction and use equilibrium
constants (Kc), to predict qualitatively, the relative amounts of reactants and products (equilibrium position)
when Kc is very small the follow assumption can be made: [reactants]initial ≈ [reactants]equilibrium
3.1.3.3 deduce the extent of a reaction from the magnitude of the equilibrium constant
3.1.3.4 use appropriate mathematical representation to solve problems, including calculating equilibrium constants
and the concentration of reactants and products.
3.1.4 Properties of Acids and Bases
3.1.4.1 understand that acids are substances that can act as proton (hydrogen ion) donors and can be classified as
monoprotic or polyprotic depending on the number of protons donated by each molecule of the acid
1
3.1.4.2 distinguish between strong and weak acids and bases in terms of the extent of dissociation, reaction with water
and electrical conductivity and distinguish between the terms strong and concentrated for acids and bases.
3.1.5 pH scale
3.1.5.1 understand that water is a weak electrolyte and the self-ionisation of water is represented by Kw = [H+][OH–]; Kw
can be used to calculate the concentration of hydrogen ions from the concentration of hydroxide ions in a solution
Kw is taken to be 1×10–14 at 25°C and is given in the Chemistry formula and data booklet.
3.1.5.2 understand that the pH scale is a logarithmic scale and the pH of a solution can be calculated from the
concentration of hydrogen ions using the relationship pH = –log10 [H+]
3.1.5.3 use appropriate mathematical representation to solve problems for hydrogen ion concentration [H+(aq)], pH,
hydroxide ion concentrations [OH–(aq)] and pOH.
3.1.6 Bronsted-Lowry Model
3.1.6.1 recognise that the relationship between acids and bases in equilibrium systems can be explained using the
Brønsted-Lowry model and represented using chemical equations that illustrate the transfer of hydrogen ions (protons)
between conjugate acid-base pairs
3.1.6.2 recognise that amphiprotic species can act as Brønsted-Lowry acids and bases
3.1.6.3 identify and deduce the formula of the conjugate acid (or base) of any Brønsted-Lowry base (or acid)
3.1.6.4 appreciate that buffers are solutions that are conjugate in nature and resist a change in pH when a small
amount of an acid or base is added; Le Châtelier’s principle can be applied to predict how buffer solutions respond to
the addition of hydrogen ions and hydroxide ions.
Buffer calculations are not required.
3.1.7 Dissociation Constants
3.1.7.1 recognise that the strength of acids is explained by the degree of ionisation at equilibrium in aqueous solution,
which can be represented with chemical equations and equilibrium constants (Ka)
3.1.7.2 determine the expression for the dissociation constant for weak acids (Ka) and weak bases (Kb) from balanced
chemical equations
Students should consider hydrochloric, nitric and sulfuric acids as examples of strong acids, and carboxylic and carbonic
acids (aqueous carbon dioxide) as weak acids.
3.1.7.3 analyse experimental data to determine and compare the relative strengths of acids and bases
3.1.7.4 use appropriate mathematical representation to solve problems, including calculating dissociation constants (Ka
and Kb) and the concentration of reactants and products.
3.1.8 Acid-base indicators
3.1.8.1 understand that an acid-base indicator is a weak acid or a weak base where the components of the conjugate
acid-base pair have different colours; the acidic form is of a different colour to the basic form
3.1.8.2 explain the relationship between the pH range of an acid-base indicator and its pKa value
3.1.8.3 recognise that indicators change colour when the pH = pKa and identify an appropriate indicator for a titration,
given equivalence point of the titration and pH range of the indicator. The colour change can be considered to take
place over a range of pKa ± 1.
3.1.9 Volumetric Analysis
3.1.9.1 distinguish between the terms end point and equivalence point
3.1.9.2 recognise that acid-base titrations rely on the identification of an equivalence point by measuring the associated
change in pH, using chemical indicators or pH meters, to reveal an observable end point
3.1.9.3 sketch the general shapes of graphs of pH against volume (titration curves) involving strong and weak acids and
bases. Identify and explain their important features, including the intercept with pH axis, equivalence point, buffer
region and points where pKa = pH or pKb = pOH
2
3.1.9.4 use appropriate mathematical representations and analyse experimental data and titration curves to solve
problems and make predictions, including using the mole concept to calculate moles, mass, volume and concentration
from volumetric analysis data.
Mandatory Practical Acid-base titration to calculate the concentration of a solution with reference to a standard
solution.
3
3.1.1 Chemical equilibrium
3.1.1.1 recognise that chemical systems may be open (allowing matter and energy to be exchanged with
the surroundings) or closed (allow energy, but not matter, to be exchanged with the surroundings)
3.1.1.2 understand that physical changes are usually reversible, whereas only some chemical reactions are
reversible
3.1.1.3 appreciate that observable changes in chemical reactions and physical changes can be described
and explained at an atomic and molecular level
3.1.1.4 symbolise equilibrium equations by using β‡Œ in balanced chemical equations
3.1.1.5 understand that, over time, physical changes and reversible chemical reactions reach a state of
dynamic equilibrium in a closed system, with the relative concentrations of products and reactants
defining the position of equilibrium
3.1.1.6 explain the reversibility of chemical reactions by considering the activation energies of the forward
and reverse reactions
3.1.1.7 analyse experimental data, including constructing and using appropriate graphical representations
of relative changes in the concentration of reactants and product against time, to identify the position of
equilibrium.
3.1.1.1 recognise that chemical systems may be open (allowing matter and energy
to be exchanged with the surroundings) or closed (allow energy, but not matter, to
be exchanged with the surroundings)
Define the following and give two examples of each:
Open system
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Closed system
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4
Explain why dynamic equilibrium can only be established in a closed system.
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Exercises
Textbook: Questions 1, 4, 5, 6 Page 13,14,
Question 1 page 44
Question 8, 14 page 45
5
3.1.1.2 understand that physical changes are usually reversible, whereas only some
chemical reactions are reversible
Define:
Reversible reaction
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Give two examples of physical changes that are reversible. Write chemical equations to explain the
process occurring.
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Give two examples of chemical reactions that are reversible. Write chemical equations for each
example. You can find some examples in your textbook.
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P 13 questions 2,3, 6
P 44 q2,
6
3.1.1.3 appreciate that observable changes in chemical reactions and physical
changes can be described and explained at an atomic and molecular level
Describe at a molecular level, any changes that would still occur once the system above has reached
equilibrium.
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Explain, at a molecular level, any observable changes that would occur as the above reaction
proceeds towards equilibrium.
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7
When red mercury(II) oxide is heated it decomposes as shown in the equation below.
Explain, at an atomic level, any observable changes that would occur in the mixture as it
approaches equilibrium.
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Explain at a molecular level, what is occurring to the reactants and products of the following
reaction at equilibrium.
𝑁2(𝑔) + 𝑂2(𝑔) β‡Œ 2𝑁𝑂(𝑔) Δ𝐻 = +180.5 π‘˜π½π‘šπ‘œπ‘™ −1
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P 14 numbers 4, 8,9
P 45 no 9,
P 48 no 37 38, 39
8
3.1.1.4 symbolise equilibrium equations by using β‡Œ in balanced chemical equations
Write an equation to represent the equilibrium that exists between liquid water and water vapour
in a closed water bottle.
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P 46 no 20
9
3.1.1.5 understand that, over time, physical changes and reversible chemical
reactions reach a state of dynamic equilibrium in a closed system, with the relative
concentrations of products and reactants defining the position of equilibrium
Below is the equation representing the Haber process.
Explain the diagram above, with reference to the Haber process.
Why has only 0.6 moles of ammonia formed rather than 2 moles, even though 1.0 moles of nitrogen
gas and 3.0 moles of hydrogen gas were initially present?
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P 14 nos 9
P 45 no 16
P 46 no 21, 32, 33 34
10
3.1.1.6 explain the reversibility of chemical reactions by considering the activation
energies of the forward and reverse reactions
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Exercises
P 14 no 7
11
3.1.1.7 analyse experimental data, including constructing and using appropriate
graphical representations of relative changes in the concentration of reactants and
product against time, to identify the position of equilibrium.
Identify on the graph below, the point at which equilibrium is established.
Identify the reactants and the products from the graph below.
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Describe the reaction that has occurred including the changes in amounts of each substance.
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12
Identify when the system below first reaches equilibrium.
Identify how many times the system reaches equilibrium.
13
Exercises
P 44 no 4
P 45 no 15
3.1.2 Factors that affect equilibrium
3.1.2.1 explain and predict the effect of temperature change on chemical systems at equilibrium by considering the
enthalpy change for the forward and reverse reactions
3.1.2.2 explain the effect of changes of concentration and pressure on chemical systems at equilibrium by applying
collision theory to the forward and reverse reactions
3.1.2.3 apply Le Châtelier’s principle to predict the effect changes of temperature, concentration of chemicals, pressure
and the addition of a catalyst have on the position of equilibrium and on the value of the equilibrium constant.
3.1.2.1 explain and predict the effect of temperature change on chemical systems at
equilibrium by considering the enthalpy change for the forward and reverse reactions
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14
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15
Predict the effect that an increase in temperature will have on the reaction below.
2X(g) + Y2(g)
X
Z(g)
ΔH = –100 kJ
Y2
Z
Keq
A decrease
1
by
2
decrease
increase
increase
B increase
1
by
2
increase
decrease
decrease
C
decrease
by 2
decrease
increase
increase
D increase
by 2
increase
decrease
decrease
The reaction between bromine and chlorine is shown below.
Bromine and chlorine were placed in a sealed vessel and allowed to reach equilibrium.
Predict the effect that increasing the temperature of the reaction between bromine and
chlorine will have on the concentration of the contents of the vessel. Show your reasoning.
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Exercises
P 31 3,
P 48 no 36
16
3.1.2.2 explain the effect of changes of concentration and pressure on chemical systems at
equilibrium by applying collision theory to the forward and reverse reactions
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17
For the equilibrium,
0.8 mol of nitrogen and 0.4 mol of oxygen were placed in a closed vessel and allowed to
reach equilibrium, at which time 0.6 mol of nitrogen remained.
Using the grid below, construct the graph of the relative changes in concentration in the
vessel.
18
Exercises
P31 no 3, 4,5
P 45 no 10, 11,
P 45 no 1`7
P 46 no 18, 19,
3.1.2.3 apply Le Châtelier’s principle to predict the effect changes of temperature,
concentration of chemicals, pressure and the addition of a catalyst have on the position of
equilibrium and on the value of the equilibrium constant.
State Le Chatelier’s Principle
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The contact process is an important industrial process for making sulfuric acid (H2SO4). This process
occurs in three stages.
a) Explain which of the stages would be affected by a change in pressure. (2 marks)
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19
20
What effect do each of the following changes have on the equilibrium position for this reversible
reaction?
𝑃𝐢𝑙5(𝑔) + β„Žπ‘’π‘Žπ‘‘ β‡Œ 𝑃𝐢𝑙3(𝑔) + 𝐢𝑙2(𝑔)
(a)
(b)
(c)
(d)
addition of Cl2
increase of pressure
removal of heat
removal of PCl3
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How is the equilibrium position of this reaction affected by the following changes?
𝐢(𝑠) + 𝐻2 𝑂(𝑔) + β„Žπ‘’π‘Žπ‘‘ β‡Œ 𝐢𝑂(𝑔) + 𝐻2(𝑔)
(a)
(b)
(c)
(d)
lowering the temperature
increasing the pressure
removing H2
adding H2
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21
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What effect does each change have on the equilibrium position of this reaction?
𝑁2(𝑔) + 3𝐻2(𝑔) ⇋ 2𝑁𝐻3(𝑔) + 92 π‘˜π½
(a)
(b)
(c)
(d)
addition of heat
increase in pressure
addition of catalyst
removal of heat
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Exercises
P 22 numbers 1,2,3 4
P 30 numbers 1,2
P 31 no 7,8,9
P 44 no 3,7,
22
3.1.3 Equilibrium constants
3.1.3.1 understand that equilibrium law expressions can be written for homogeneous and heterogeneous systems
and that the equilibrium constant (Kc), at any given temperature, indicates the relationship between product and
reactant concentrations at equilibrium
3.1.3.2 deduce the equilibrium law expression from the equation for a homogeneous reaction and use equilibrium
constants (Kc), to predict qualitatively, the relative amounts of reactants and products (equilibrium position)
when Kc is very small the follow assumption can be made: [reactants]initial ≈ [reactants]equilibrium
3.1.3.3 deduce the extent of a reaction from the magnitude of the equilibrium constant
3.1.3.4 use appropriate mathematical representation to solve problems, including calculating equilibrium
constants and the concentration of reactants and products.
3.1.3.1 understand that equilibrium law expressions can be written for homogeneous and
heterogeneous systems and that the equilibrium constant (Kc), at any given temperature,
indicates the relationship between product and reactant concentrations at equilibrium
Explain what Kc tells you about the relationship between products and reactants in a system at
equilibrium.
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23
Compare homogeneous and heterogenous systems and give examples of each by writing an
equilibrium equation highlighting both types of systems.
Why is it important to understand the difference between them in terms of writing the equilibrium
expressions?
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P 41 no 1,2,3
P 44 no 5, 6 , 12
P 46 no 22, 23,
3.1.3.2 deduce the equilibrium law expression from the equation for a homogeneous
reaction and use equilibrium constants (Kc), to predict qualitatively, the relative amounts
of reactants and products (equilibrium position)
when Kc is very small the follow assumption can be made: [reactants]initial ≈
[reactants]equilibrium
Consider the following reaction:
2H2(g) + S2(g) β‡Œ 2H2O(g) + 2Cl2(g)
Kc = 9.4 x 105 at 750°C
A mixture of the above was allowed to come to equilibrium in a closed 2.0L container at 750°C. The
equilibrium concentrations of H2 and H2S gases were analysed and found to be 0.234 M and 0.442
M respectively.
a. State what the value of the equilibrium constant for this reaction tells you about the extent
of the reaction.
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b. Show an expression for the equilibrium constant for this reaction.
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24
c. Calculate the equilibrium concentration of S2(g) in the mixture.
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P 41 no 4, 5, 6,7,8,9, 10,
P 45 no 13
P 46 no 24, 26, 27, 28, 29,30
3.1.3.3 deduce the extent of a reaction from the magnitude of the equilibrium constant
Complete the following:
If Kc < 10-4, there is a negligible __________ reaction and mainly ____________ present at equilibrium. The
position of equilibrium is to the ___________.
If 10-4 < Kc < 104, the equilibrium mixture consists of significant amounts of both __________ and
____________.
If Kc > 104, there is extensive ____________ reaction and mainly ______________ present at equilibrium. The
position of equilibrium is to the __________.
P 42 no 11,12
25
3.1.3.4 use appropriate mathematical representation to solve problems, including
calculating equilibrium constants and the concentration of reactants and products.
An equilibrium mixture of CH4, H2O, H2 and CO was prepared in a 2.00L flask by adding 0.600 mol of
CH4 and 0.400 mol of H2O to the reaction vessel. At equilibrium there was 0.110 mol of CO present.
a. Determine the amounts of CH4, H2O and H2 at equilibrium.
b. Calculate the equilibrium concentration of CH4, H2O, H2 and CO.
c. Calculate the equilibrium constant, Kc, for the reaction.
Exercises
P 42 no 13, 14, 15, 16, 17,28
P 46 no 25, 31,
P 48 no 35
P 49 no 40
26
3.1.4 Properties of Acids and Bases
3.1.4.1 understand that acids are substances that can act as proton (hydrogen ion) donors and can be classified as
monoprotic or polyprotic depending on the number of protons donated by each molecule of the acid
3.1.4.2 distinguish between strong and weak acids and bases in terms of the extent of dissociation, reaction with water and
electrical conductivity and distinguish between the terms strong and concentrated for acids and bases.
3.1.4.1 understand that acids are substances that can act as proton (hydrogen ion) donors
and can be classified as monoprotic or polyprotic depending on the number of protons
donated by each molecule of the acid
Complete the table below
Type of Acid
Monoprotic
Number of
protons to
donate
Examples
Equation for dissociation
HNO3,
CH3COOH
HNO3(aq) + H2O(l) → NO3- (aq) + H3O+(aq)
Diprotic
Triprotic
P57 no 5,6,8
P62 no 3
P 83 no 12
27
3.1.4.2 distinguish between strong and weak acids and bases in terms of the extent of
dissociation, reaction with water and electrical conductivity and distinguish between the
terms strong and concentrated for acids and bases.
Strong
Acids
Readily donates protons and completely
dissociates in water.
E.g.
HCl(aq) + H2O(l) → Cl- (aq) + H3O+(aq)
Weak
Does not readily __________ protons and
_________ dissociates in water.
Bases
Readily _________ protons and __________
dissociates in water
Does not readily ________ protons and
_____________ dissociates in water.
Draw a diagram to illustrate the differences between the terms strong and concentrated.
Explain how measurements of electrical conductivity can be used to distinguish between strong and
weak acids.
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28
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Exercises
P 62 no 1,2,4.,5
P83 no 1,13
3.1.5 pH Scale
3.1.5.1 understand that water is a weak electrolyte and the self-ionisation of water is represented by Kw = [H+][OH–]; Kw can
be used to calculate the concentration of hydrogen ions from the concentration of hydroxide ions in a solution
Kw is taken to be 1×10–14 at 25°C and is given in the Chemistry formula and data booklet.
3.1.5.2 understand that the pH scale is a logarithmic scale and the pH of a solution can be calculated from the concentration
of hydrogen ions using the relationship pH = –log10 [H+]
3.1.5.3 use appropriate mathematical representation to solve problems for hydrogen ion concentration [H+(aq)], pH,
hydroxide ion concentrations [OH–(aq)] and pOH.
3.1.5.1 understand that water is a weak electrolyte and the self-ionisation of water is
represented by Kw = [H+][OH–]; Kw can be used to calculate the concentration of
hydrogen ions from the concentration of hydroxide ions in a solution
Kw is taken to be 1×10–14 at 25°C and is given in the Chemistry formula and data booklet.
Complete the following reaction to represent the self-ionisation of water.
H2O(l) + H2O(l) β‡Œ
Calculate the pH of a 0.001M NaOH solution.
P 70 no 2,4,5
P 84 no 16,
29
3.1.5.2 understand that the pH scale is a logarithmic scale and the pH of a solution can be
calculated from the concentration of hydrogen ions using the relationship pH = –log10 [H+]
Calculate the pH for each of the following solutions.
Solution
0.010 M HCl
Calculation
0.050 M H2SO4
0.010 M CH3COOH
0.010 M NaOH
0.00050 M Ba(OH)2
P 70 no 3,6
P 84 no 17, 18 19,20,
30
3.1.5.3 use appropriate mathematical representation to solve problems for hydrogen ion
concentration [H+(aq)], pH, hydroxide ion concentrations [OH–(aq)] and pOH.
Complete the following mathematical relationships.
a. pH =
b. [H3O+] =
c. pOH =
d. [H3O+] x [OH-] =
e. AT 25°C, the value of Kw =
f.
At 25°C, pH + pOH =
Calculate the pH of a solution formed by mixing 20.00 mL of 0.30 M HCl with 30.00 mL or 0.15 M
HNO3
Calculate the pH of the final solution obtained by mixing 20 mL of 0.20 M KOH solution with 80 mL of
0.20 M HCl solution.
31
Exercises
P 84 no 21,22,23,24,25.26,27,
P 85 no 31
3.1.6 Brønsted-Lowry acids and bases
3.1.6.1 recognise that the relationship between acids and bases in equilibrium systems can be explained using the BrønstedLowry model and represented using chemical equations that illustrate the transfer of hydrogen ions (protons) between
conjugate acid-base pairs
3.1.6.2 recognise that amphiprotic species can act as Brønsted-Lowry acids and bases
3.1.6.3 identify and deduce the formula of the conjugate acid (or base) of any Brønsted-Lowry base (or acid)
3.1.6.4 appreciate that buffers are solutions that are conjugate in nature and resist a change in pH when a small amount of
an acid or base is added; Le Châtelier’s principle can be applied to predict how buffer solutions respond to the addition of
hydrogen ions and hydroxide ions.
Buffer calculations are not required.
3.1.6.1 recognise that the relationship between acids and bases in equilibrium systems
can be explained using the Brønsted-Lowry model and represented using chemical
equations that illustrate the transfer of hydrogen ions (protons) between conjugate acidbase pairs
Complete the table below.
Ionic equation
NH3(aq) + H2O(l) β‡Œ
Conjugate pairs
NH3 and NH4+, H2O and OH-
HCl(aq) + OH-(aq) →
H2SO4(aq) + H2O(l) →
CH3COOH(aq) + OH- →
P 57 no 3,7,
P 83 no 7,9,10,11,
32
3.1.6.2 recognise that amphiprotic species can act as Brønsted-Lowry acids and bases
What is an amphiprotic substance?
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Give two examples of substances which are amphiprotic and write chemical equations to explain.
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P 57 no 6,8,9
3.1.6.3 identify and deduce the formula of the conjugate acid (or base) of any BrønstedLowry base (or acid)
Label the acid, base, conjugate acid and conjugate base for the equation below.
HCl(aq) + OH-(aq) → Cl-(aq) + H2O(l)
P 57 no 1,2,4 5
33
3.1.6.4 appreciate that buffers are solutions that are conjugate in nature and resist a
change in pH when a small amount of an acid or base is added; Le Châtelier’s principle can
be applied to predict how buffer solutions respond to the additionn of hydrogen ions and
hydroxide ions.
Buffer calculations are not required.
Define ‘buffer’
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Explain why a mixture of HCl and NaOH does not form a buffer solution.
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34
P 72 no 2,3 4,
35
3.1.7 Dissociation Constants
3.1.7.1 recognise that the strength of acids is explained by the degree of ionisation at equilibrium in aqueous solution, which
can be represented with chemical equations and equilibrium constants (Ka)
3.1.7.2 determine the expression for the dissociation constant for weak acids (Ka) and weak bases (Kb) from balanced
chemical equations
Students should consider hydrochloric, nitric and sulfuric acids as examples of strong acids, and carboxylic and carbonic acids
(aqueous carbon dioxide) as weak acids.
3.1.7.3 analyse experimental data to determine and compare the relative strengths of acids and bases
3.1.7.4 use appropriate mathematical representation to solve problems, including calculating dissociation constants (Ka and
Kb) and the concentration of reactants and products.
3.1.7.1 recognise that the strength of acids is explained by the degree of ionisation at
equilibrium in aqueous solution, which can be represented with chemical equations and
equilibrium constants (Ka)
Compare strong and weak acids. Use equations and provide examples to illustrate your answer.
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P 76 no 1,
P 83 no 4,5
36
3.1.7.2 determine the expression for the dissociation constant for weak acids (Ka) and
weak bases (Kb) from balanced chemical equations
Students should consider hydrochloric, nitric and sulfuric acids as examples of strong
acids, and carboxylic and carbonic acids (aqueous carbon dioxide) as weak acids.
Write the expression for the dissociation constant for the following acids and bases.
CH3COOH
H2CO3
NH3
P 76 no 1,2,3,4
3.1.7.3 analyse experimental data to determine and compare the relative strengths of
acids and bases
Revise all questions from experiments 3.1.4 and 3.1.5 where you measured the pH of some
acids and bases, and you measured the conductivity of acids and bases.
When using pH or electrical conductivity to compare strong and weak acids an bases, it is
important to keep the concentration of each substance the same. Explain why.
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3.1.7.4 use appropriate mathematical representation to solve problems, including
calculating dissociation constants (Ka and Kb) and the concentration of reactants and
products.
The value of Ka or Kb is a measure of the __________ of an acid or base, or the degree of
dissociation of an acid or base. The ____________ the value, the stronger the acid or base.
Four acids, W, X, Y and Z, with concentrations of 0.10 M, have pH values of 2.4, 1.0, 6.6 and
3.1 respectively. Determine and explain:
Which, if any, is completely ionised.
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Which if any is almost completely un-ionised.
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Their order in increasing acid strength (weakest to strongest)
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Lactic acid, HC3H5O3, which is found in milk, has a Ka of 1.38 x 10-4. Calculate the percentage
dissociation of lactic acid in a 0.100 M solution.
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The concentration of CH3COOH at 25°C is 1.00 M. The value of Ka is 1.75 x 10-5. Calculate the
concentration of the ethanoate ion at this temperature.
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39
Calculate the pH of a 0.500 M solution of ammonia if the Kb at 25°C is 1.80 x 10-5.
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3.1.8 Acid-base indicators
3.1.8.1 understand that an acid-base indicator is a weak acid or a weak base where the components of the conjugate acidbase pair have different colours; the acidic form is of a different colour to the basic form
3.1.8.2 explain the relationship between the pH range of an acid-base indicator and its pKa value
3.1.8.3 recognise that indicators change colour when the pH = pKa and identify an appropriate indicator for a titration, given
equivalence point of the titration and pH range of the indicator. The colour change can be considered to take place over a
range of pKa ± 1.
3.1.8.1 understand that an acid-base indicator is a weak acid or a weak base where the
components of the conjugate acid-base pair have different colours; the acidic form is of a
different colour to the basic form.
By representing the acid form of an indicator as HIn, write a reaction to show the reversible
reaction which occurs when the acid dissociates in water to form its conjugate base, In -.
40
3.1.8.2 explain the relationship between the pH range of an acid-base indicator and its pKa
value
Consider the following indicator solution equilibrium:
HIn(aq) + H2O(l) β‡Œ H3O+(aq) + In-(aq)
Ka at 25
= 1.0 x 10-7
Write an expression for the acidity constant for the above reaction.
Calculate the pH of the solution when the acid and base forms are present in equal
concentrations, i.e. [HIn] = [In-]. What would you see happening at this point?
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P82 no 2,3,4,6,7
P 83 no 6,14
41
3.1.8.3 recognise that indicators change colour when the pH = pKa and identify an
appropriate indicator for a titration, given equivalence point of the titration and pH range
of the indicator. The colour change can be considered to take place over a range of pKa ±
1.
42
P82 no 5,7b
P 83 no 2, 3, 15
P 84 no 29,30
P 100 no 10, 11
P 113 no 3,
3.1.9 Volumetric Analysis
3.1.9.1 distinguish between the terms end point and equivalence point
3.1.9.2 recognise that acid-base titrations rely on the identification of an equivalence point by measuring the associated
change in pH, using chemical indicators or pH meters, to reveal an observable end point
3.1.9.3 sketch the general shapes of graphs of pH against volume (titration curves) involving strong and weak acids and
bases. Identify and explain their important features, including the intercept with pH axis, equivalence point, buffer region and
points where pKa = pH or pKb = pOH
3.1.9.4 use appropriate mathematical representations and analyse experimental data and titration curves to solve problems
and make predictions, including using the mole concept to calculate moles, mass, volume and concentration from volumetric
analysis data.
3.1.9.1 distinguish between the terms end point and equivalence point
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P 99 no 2,
3.1.9.2 recognise that acid-base titrations rely on the identification of an equivalence
point by measuring the associated change in pH, using chemical indicators or pH meters,
to reveal an observable end point
P 99 no 3,
P 113 no 5,6.7, 8,
P 113 no 15,19
43
3.1.9.3 sketch the general shapes of graphs of pH against volume (titration curves)
involving strong and weak acids and bases. Identify and explain their important features,
including the intercept with pH axis, equivalence point, buffer region and points where
pKa = pH or pKb = pOH
P84 no 28,
P 113 no 1,2,
P 114 no 13. 20,
44
3.1.9.4 use appropriate mathematical representations and analyse experimental data and titration
curves to solve problems and make predictions, including using the mole concept to calculate
moles, mass, volume and concentration from volumetric analysis data.
P 99 no 4,6, 7, 8, 9,
P 109 no 4,5,6,7
P 113 no 4,
P 114 no 9,10,11,12,16,17, 18, 21
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