OCR A-Level Chemistry B H433
Development of Practical Skills in Chemistry
Elements of Life
Developing Fuels
Elements From the Sea
The Ozone Story
What's in a Medicine?
The Chemical Industry
Polymers and Life
Oceans
Developing Metals
Colour by Design
Chemical Literacy
Mathematical Skills in Chemistry
The Chemical Industry
- 16 subtopics
- 43 things to know
- Components 01, 02 and 03
What The Chemical Industry covers
The storyline that carries kinetics and the quantitative treatment of equilibrium: rate equations and orders, half-lives, the Arrhenius equation, the rate-determining step, what changes an equilibrium constant, and the chemistry and economics of an industrial process.
Where it is assessed
Components 01, 02 and 03
Storyline content, drawn on by all three written papers.
Check the OCR specification ↗The 16 subtopics
Each one has its own page.
- Rate equations, order and the rate constantRecall questions on the definition of rate and its units, what order means, and why the orders cannot be read off the balanced equation.Open →
- Deducing the units of k and rate calculationsRecall questions on working out the units of k for each overall order, and calculating a rate or a concentration from a rate equation.Open →
- Half-livesRecall questions on which order has a constant half-life, how successive half-lives behave for each order, and k = ln 2 / t½.Open →
- Continuous monitoring, quenching and the initial rates methodRecall questions on the three experimental approaches, using a colorimeter, and why the initial rate is the one measured.Open →
- Reading order from concentration-time and rate-concentration graphsRecall questions on the shapes for each order on both kinds of graph, drawing a tangent, and what a linear gradient gives.Open →
- The Arrhenius equation and what each symbol meansRecall questions on the exponential and logarithmic forms, what Ea, A, R and T each represent, and why k rises steeply with temperature.Open →
- The ln k against 1/T plot and finding the activation enthalpyRecall questions on which quantities are plotted, what the gradient and intercept give, and calculating Ea and A from them.Open →
- Rate-determining step and mechanismRecall questions on what the rate-determining step is, what the orders imply about which species take part, and testing a proposed mechanism.Open →
- Effect of conditions on the magnitude of the equilibrium constantRecall questions on why only temperature changes Kc, what heating does to an exothermic and an endothermic reaction, and what a catalyst does not do.Open →
- Economic operating conditions for an industrial processRecall questions on balancing yield against rate, why very high pressure is not always used, and why a catalyst sets a lower temperature limit.Open →
- Writing a Kc expression and deducing its unitsRecall questions on homogeneous equilibria, writing the expression from a balanced equation, and deducing the units for each case.Open →
- ICE-table calculations and measuring Kc experimentallyRecall questions on using an initial, change and equilibrium table, converting amounts to concentrations, and measuring Kc for an esterification.Open →
- Chemical reactions in industrial processesRecall questions on the stages of nitric and sulfuric acid manufacture, why oleum is made, and the green case for a carbonylation route.Open →
- Nitrogen, ammonia and the ammonium ionRecall questions on why nitrogen is unreactive, the shape and bond angle of ammonia and of the ammonium ion, and how the dative bond forms.Open →
- Oxidation states of nitrogen and the tests for nitrate and ammoniumRecall questions on the oxidation state of nitrogen in its oxides and ions, and the Devarda's alloy and hydroxide tests.Open →
- Costs, benefits and risks of industrial processesRecall questions on saleable co-products, the double cost of a by-product, energy recovery, plant capacity and location.Open →
What you need to know
Answer each one before you reveal it.
What is the overall order, and what happens to the rate when a zero-order and a first-order concentration are changed?
What does doubling a second-order concentration do, and what are the units of k for zero and first order overall?
Which order has a half-life independent of concentration, how do successive half-lives show first-order kinetics, and how do they behave for zero order?
How do successive half-lives behave for second order, and how are the half-life and the rate constant related for a first-order reaction?
What concentration remains 150 s after a first-order reaction starts at 0.80 mol dm⁻³ with t½ = 50 s, why should more than one half-life be measured, and how long until 87.5% of a first-order reactant with t½ = 4.0 min has gone?
What is the symbol used for half-life?
What is continuous monitoring, how is a colorimeter used, and what is the quenching method for?
Why is a thermostatted water bath used, why is the initial rate measured, and how is a rate read off a curve?
Why must a tangent be used rather than a chord, why is the gradient of a concentration–time graph negative while the rate is positive, and how is first order recognised from the graph?
Doubling [A] quadruples the rate, while trebling [B] leaves it unchanged. Write the rate equation.
What is the straight-line form of the Arrhenius equation, what does each symbol mean, and what is the gas constant?
Why does k rise steeply with temperature, what does a larger activation enthalpy do, and which quantities are plotted?
What is A when the intercept ln A is 24.0, what temperature does 1/T = 3.20 × 10⁻³ K⁻¹ correspond to, and how does a ln k against 1/T plot show k rising with temperature?
What is the rate-determining step, how many particles take part up to it when rate = k[A]²[B], and which species are involved in it when A + 2B + C → products has rate = k[A][B]?
A reaction is found to be zero order with respect to one reactant. What does this reveal about the mechanism?
Why is a step involving three particles colliding at once considered unlikely?
Can kinetic evidence ever prove a mechanism is correct?
Which single condition changes Kc, and what happens to it on heating an exothermic and an endothermic reaction?
What do a catalyst and a change of concentration each do to the magnitude of Kc and to the position of equilibrium?
How does Kc change when the exothermic ammonia equilibrium is cooled, and what do a very large and a very small Kc indicate?
Explain why quoting a value of Kc without a temperature is meaningless.
Which two chemical considerations are balanced when choosing conditions, why is very high pressure not always used, and why do many catalysts set a lower limit on the operating temperature?
What is meant by recycling unreacted feedstock, and why is it done?
Given data showing that yield rises only slightly between 200 and 400 atmospheres, what would you conclude?
What role does the physical state of a catalyst play in plant design?
What is a homogeneous equilibrium, what is the general Kc expression, and what are the units for the dinitrogen tetroxide equilibrium?
What are the units of Kc for the hydrogen iodide, sulfur trioxide and ammonia equilibria?
When does Kc have no units, how is the change in amount fixed by the stoichiometry, and why is the flask volume not needed to find Kc for ethanoic acid + ethanol ⇌ ethyl ethanoate + water?
When Kc is measured experimentally, why must the reaction mixture be left for a long time before it is sampled?
What are the oxidation states of nitrogen in NO and NO₂, why is 3NO₂ + H₂O → 2HNO₃ + NO a disproportionation, and which stage of S + O₂ → SO₂ then 2SO₂ + O₂ ⇌ 2SO₃ is an equilibrium?
Why is sulfur trioxide absorbed in concentrated sulfuric acid rather than water, what happens when the oleum is diluted, and why is making ethanoic acid by CH₃OH + CO → CH₃COOH attractive on green grounds?
Why is nitrogen gas unreactive, what are the shape and bond angle of ammonia, and how is the ammonium ion formed?
Why are all four N-H bonds in the ammonium ion identical, and what is the oxidation state of nitrogen in N₂O and NO₂?
What are the oxidation states of nitrogen in the nitrate(V) ion, the nitrate(III) ion and the ammonium ion?
How does a saleable co-product improve the economics of a process, why is an unwanted by-product a double cost, and how does raising the yield from 60% to 75% change the raw material needed?
Why is energy recovery designed into a chemical plant, why does running below design capacity raise the cost per tonne, and how does the location of a plant affect its costs?
Why is the transport of a chemical sometimes riskier than its manufacture?
Why can the hazard of a substance never be reduced by a change in working practice, whereas the risk can?
State the usual units of rate of reaction.
Write the Arrhenius equation in its exponential form.
Nitrogen monoxide is oxidised by 2NO + O₂ → 2NO₂. Give the oxidation state of nitrogen in each oxide.
Describe the shape and bond angle of an ammonia molecule.
Take The Chemical Industry further
The same content, four other ways.
Commonly confused
Pairs that lose marks when they are blurred together.
Rate constant vs Order of reaction
Rate constant: the proportionality constant in a rate equation, which changes only with temperature. Order of reaction: the power to which a concentration is raised in the rate equation.
Rate-determining step vs Activation enthalpy
Rate-determining step: the slowest step in a mechanism, which fixes the overall rate. Activation enthalpy: the minimum energy needed by colliding particles for a reaction to occur.
Zero-order reactant vs First-order reactant
Zero-order reactant: a reactant whose concentration has no effect on the rate. First-order reactant: a reactant for which doubling the concentration doubles the rate.
Questions from this topic
Each one with the model answer underneath.
- 1
Define the rate of a chemical reaction.
Model answer
The rate of reaction is the change in concentration of a reactant or product divided by the time taken for that change.
- 2
State the usual units of rate of reaction.
Model answer
The usual units are mol dm⁻³ s⁻¹.
- 3
What is a rate equation?
Model answer
A rate equation is an expression showing how the rate depends on the concentrations of the species that affect it, of the form rate = k[A]ᵐ[B]ⁿ.
- 4
Can the orders in a rate equation be predicted from the balanced equation?
Model answer
No, orders can only be found by experiment, because they depend on the mechanism rather than on the overall stoichiometry.
- 5
Define the order of reaction with respect to a given reagent.
Model answer
It is the power to which the concentration of that reagent is raised in the experimentally determined rate equation.
- 6
Define the overall order of a reaction.
Model answer
The overall order is the sum of the individual orders with respect to each species in the rate equation.
What is inside Levo
Six ways to work the same material.
The Chemical Industry revision questions
- What does The Chemical Industry cover in OCR A-Level Chemistry B?
- 16 subtopics: rate equations, order and the rate constant, deducing the units of k and rate calculations, half-lives, continuous monitoring, quenching and the initial rates method, reading order from concentration-time and rate-concentration graphs, the arrhenius equation and what each symbol means, the ln k against 1/t plot and finding the activation enthalpy, rate-determining step and mechanism, effect of conditions on the magnitude of the equilibrium constant, economic operating conditions for an industrial process, writing a kc expression and deducing its units, ice-table calculations and measuring kc experimentally, chemical reactions in industrial processes, nitrogen, ammonia and the ammonium ion, oxidation states of nitrogen and the tests for nitrate and ammonium and costs, benefits and risks of industrial processes. Each one has its own page with questions and model answers.
- How is The Chemical Industry organised?
- By the OCR H433 specification, subtopic by subtopic, so it matches the order you are taught it in.
Every question in The Chemical Industry, on a schedule.
Attempt a question from memory, write the correct version, then attempt it again. Levo records the jump between your first attempt and your last, and brings each question back on the day you are due to forget it.
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