OCR A-Level Chemistry H432
Foundations in Chemistry
Bonding and Structure
Periodic Table and Energy
Enthalpy Changes
Chemical Equilibrium
Basic Concepts of Organic Chemistry
Core Organic Chemistry
Alkenes
Organic Synthesis
How Fast?
Physical Chemistry and Transition Elements
Acids, Bases and Buffers
Redox and Electrode Potentials
Transition Elements
Aromatic Compounds
Organic Chemistry and Analysis
Spectroscopy
How Fast?
- 10 subtopics
- 19 things to know
- Components 01 and 03
What How Fast? covers
Kinetics beyond collision theory: rate equations, orders and the rate constant, reading order from concentration-time and rate-concentration graphs, what the rate equation reveals about the mechanism, and the Arrhenius equation.
Where it is assessed
Components 01 and 03
Periodic Table, Elements and Physical Chemistry, then the unified paper.
Check the OCR specification ↗The 10 subtopics
Each one has its own page.
- Rate equations, order and the rate constantRecall questions on the meaning of order, the overall order, the role of k, half-life, and how rate depends on concentration for each order.Open →
- Deducing orders and finding the units of kRecall questions on reading order from initial rates data, the general form rate = k[A]ᵐ[B]ⁿ, why orders cannot be read off the balanced equation, and deriving the units of k.Open →
- What the rate equation reveals about the mechanismRecall questions on which species appear in the rate equation and why one may not, and on the principle and advantage of the initial rates method.Open →
- Concentration-time graphs and continuous monitoringRecall questions on the shapes for zero and first order, why a tangent rather than a chord is used, and what continuous monitoring offers.Open →
- Half-life and the rate constant of a first-order reactionRecall questions on the constant half-life of a first-order reaction, reading it from a graph, and k = ln 2 / t½.Open →
- Rate-concentration graphs and the initial rates methodRecall questions on the shapes for zero, first and second order, and on what the gradient of a linear rate-concentration graph gives.Open →
- Clock reactions, colorimetry and analysing kinetic graphsRecall questions on what a clock reaction approximates, how colorimetry follows a rate, and choosing scales, reading intercepts and drawing tangents.Open →
- The rate-determining step and testing a proposed mechanismRecall questions on what the rate-determining step is, what the orders imply about it, and the two criteria a proposed mechanism must satisfy.Open →
- Temperature, the rate constant and the Arrhenius equationRecall questions on why raising the temperature raises k, and on what Eₐ, A, R and T each represent in the Arrhenius equation.Open →
- The ln k against 1/T graph and finding the activation energyRecall questions on the logarithmic form, which graph is plotted, and what its gradient and intercept give.Open →
What you need to know
Answer each one before you reveal it.
How does rate depend on concentration for a zero-order, a first-order and a second-order reactant?
If doubling a concentration quadruples the rate, what is the order, what is the general rate equation for reactants A and B, and what decides the units of k?
Can the orders in a rate equation be predicted from the balanced chemical equation? Explain.
Which species from a reaction mechanism will appear in the rate equation?
What does a zero-order concentration–time graph look like, how does a first-order graph differ, and why is a tangent used rather than a chord?
What is characteristic of the half-life of a first-order reaction, how is it read off a concentration–time graph, and what do equal successive half-lives show?
What equation links k to the half-life, when does it apply, and what is k when t½ = 280 s?
How is first-order dependence recognised on a rate–concentration graph, why does its gradient give k, and what does a zero-order reactant give?
What is continuous monitoring in the context of reaction kinetics?
Give an example of a technique used for continuous monitoring of reaction rates.
A reaction is second order with respect to reactant A. What does this suggest about the mechanism?
If a species appears in the balanced equation but has zero order in the rate equation, what does this indicate about the mechanism?
What type of experimental evidence is used to propose and support reaction mechanisms?
How does raising the temperature change molecular energies, and why does that speed up the reaction?
What does T represent in the Arrhenius equation and in what units, what is its logarithmic form, and what does A represent?
What does R represent in the Arrhenius equation, which graph is plotted to obtain a straight line, and what does its gradient equal?
State the formula used to calculate the pre-exponential factor from the y-intercept of an Arrhenius plot.
State the general rate equation and interpret its powers.
Take How Fast? further
The same content, four other ways.
Commonly confused
Pairs that lose marks when they are blurred together.
Rate constant vs Reaction rate
Rate constant: proportionality constant linking rate with reactant concentrations. Reaction rate: change in concentration of a reactant or product per unit time.
Order of reaction vs Overall order
Order of reaction: power to which a concentration is raised in a rate equation. Overall order: sum of concentration powers in a rate equation.
Rate-determining step vs Elementary step
Rate-determining step: slowest stage controlling the overall reaction rate. Elementary step: one stage in a multi-stage reaction mechanism.
Questions from this topic
Each one with the model answer underneath.
- 1
How is rate of reaction defined in terms of concentration?
Model answer
Rate of reaction is the change in concentration of a reactant or product per unit time.
- 2
What does the order with respect to a reactant represent in a rate equation?
Model answer
The order with respect to a reactant is the power to which the concentration of that reactant is raised in the rate equation.
- 3
How is the overall order of a reaction determined from the rate equation?
Model answer
The overall order is the sum of the individual orders with respect to each reactant in the rate equation.
- 4
What is the role of the rate constant k in a rate equation?
Model answer
The rate constant k is the proportionality constant that relates the rate to the concentrations of reactants raised to their respective orders.
- 5
Define half-life in the context of chemical kinetics.
Model answer
Half-life is the time taken for the concentration of a reactant to fall to half its initial value.
- 6
What happens to the rate of reaction if the concentration of a zero-order reactant is increased?
Model answer
The rate remains unchanged; changing the concentration of a zero-order reactant has no effect on the rate.
What is inside Levo
Six ways to work the same material.
How Fast? revision questions
- What does How Fast? cover in OCR A-Level Chemistry?
- 10 subtopics: rate equations, order and the rate constant, deducing orders and finding the units of k, what the rate equation reveals about the mechanism, concentration-time graphs and continuous monitoring, half-life and the rate constant of a first-order reaction, rate-concentration graphs and the initial rates method, clock reactions, colorimetry and analysing kinetic graphs, the rate-determining step and testing a proposed mechanism, temperature, the rate constant and the arrhenius equation and the ln k against 1/t graph and finding the activation energy. Each one has its own page with questions and model answers.
- How is How Fast? organised?
- By the OCR H432 specification, subtopic by subtopic, so it matches the order you are taught it in.
Every question in How Fast?, 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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