Edexcel A Level Chemistry: 16: Kinetics II
This flashcard set explains what the rate of reaction indicates and how it is calculated. It also outlines various experimental methods for measuring reaction rates, including gas volume collection, mass loss, and color change analysis using a colorimeter.
What does rate of reaction tell you?
How fast reactants are converted to products
Key Terms
What does rate of reaction tell you?
How fast reactants are converted to products
How is rate calculated?
Change in concentration of products/time
How can rate of reaction be determined experimentally?
Gas volume
Loss of mass
Colour change
Change in pH
Titration
Electrical conductivityHow can gas volume be used to determine rate of reaction?
It can be collected in a syringe and the amount recorded at set intervals, and the ideal gas equation used to work out moles and then molar ratio
How can loss of mas be used to determine rate of reaction?
If a gas is given off, the system will lose mass, measured at regular intervals with a balance
How can colour change be used to determine rate of reaction?
Can be tracked with a colorimeter and a calibration curve plotted
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| Term | Definition |
|---|---|
What does rate of reaction tell you? | How fast reactants are converted to products |
How is rate calculated? | Change in concentration of products/time |
How can rate of reaction be determined experimentally? | |
How can gas volume be used to determine rate of reaction? | It can be collected in a syringe and the amount recorded at set intervals, and the ideal gas equation used to work out moles and then molar ratio |
How can loss of mas be used to determine rate of reaction? | If a gas is given off, the system will lose mass, measured at regular intervals with a balance |
How can colour change be used to determine rate of reaction? | Can be tracked with a colorimeter and a calibration curve plotted |
How can change in pH be used to determine rate fo reaction? | If a reaction produces or used up H+, pH can be measured to determine the change in H+ concentration |
How can titration be used to determine rate of reaction? | Small samples can be taken at regular intervals and titrated against a standard solution, change in concentration over time |
How can electrical conductivity be used to determine rate of reaction? | If the number of ions changes, so will the conductivity |
What is the rate constant? | K |
What does the value of k change with? | Temperature |
What do orders tell you? | How a reactant’s concentration affects the rate |
How can orders of reaction be calculated? | From experimental data |
What is the overall rider of a reaction? | The sum of all the orders of reaction of the reactants |
What does a zero order concentration-time graph look like? | Straight line, top to bottom of Y axis |
What does a zero-order rate-concentration graph look like? | Horizontal line |
What does a first order concentration-time graph look like? | Curve, top to bottom |
What does a first order rate-concentration graph look like? | Directly proportional |
What does a second order concentration-time graph look like? | Steep curve, top to bottom |
What does a second order rate-concentration time graph look like? | Curve, bottom to top |
What is half life? | The time taken for half the reactant to be used up |
How can orders of reaction be worked out? | Using the initial rates method |
| A clock reaction |
How is an initial rates method carried out? | Carrying out separate experiments using different initial concentrations of one reactant, then seeing how the change in Italy concentrations affects the rate |
What is done in a clock reaction? | You measure the time taken or a set amount of product to form and how it changes as the concentrations vary |
What assumptions are made in clock reactions? | The concentration of arch reactant doesn’t change significantly over th period of the reaction |
What happens at the end of a clock reaction? | There’s an easily observable end point as there is a sudden increase in the concentration of a product as the limiting reactant is used up |
What is an example of a clock reaction? | The iodine clock reaction |
What is the reaction that occurs in the iodine clock? | H2O2 + 2I- + 2H+ ——> 2H2O + I2 |
What is the indicator used? | Starch |
Why is sodium thiosulfate added to the mixture? | To react instantaneously with any iodine that forms |
What happens when the thiosulfate is used up? | The iodine becomes obvious with the indicator as it is allowed to form ithout reacting with the thiosulfate |
Which reactant’s concentrations are varied? | The iodide or hydrogen peroxide |
What is an example of a continuous monitoring method? | Titrations the reaction between iodine and propanone |
What is the equation for the reaction between iodine and propanone? | CH3COCH3 + I2 —H+—> CH3COCH2I + H+ + I- |
Why is sodium hydrogencarbnate added to samples of iodine-propanone before titrating? | To stop the reaction by neutralising the acid |
What do rate equations link? | Rate of reaction and reactant concentrations |
What is a rate equation? | Rate = k[A]^m [B]^n |
The bigger k is… | …the faster the reaction |
What can the rate constant be calculated from? | The orders and rate of reaction |
How can k be calculated? | Rate of reaction / concentrations and orders |
What is the rate determining step? | The slowest step in a multi-step reaction |
What does it indicate if a reactant appears in the rate equation? | That it features in the rate determining step |
What is the order of reaction with respect to a reactant? | Shows the number of molecules of that reactant that are involved in or before the rate determining step |
What can halogenoalkanes be hydrolysed by? | Hydroxide ions |
What do halogenoalkanes undergo? | Nucleophillic substitution |
By what mechanism are primary halogenoalkanes hydrolysed? | SN2 |
By what mechanism are tertiary halogenoalkanes hydrolysed? | SN1 |
What does an SN2 reaction include? | A transition state |
What does an SN1 reaction include? | An intermediate carbocation |
By what mechanism do secondary halogenoalkanes react? | SN1 or SN2 |
What is the Arrhenius equation? | k = Ae^(-Ea/RT) |
What is the relationship between activation energy and k? | As Ea gets bigger, k gets smaller |
| As temperature increases, so does k |
What is the gradient of an Arrhenius graph? | -Ea/R |
How can you find the activation energy from the Arrhenius graph? | By multiplying the gradient by R |
What are homogeneous catalysts? | In the same state as the reactant |
What are heterogeneous catalysts? | In a different physical state to the reactants |
How do solid heterogeneous catalysts work? | They provide a surface for the reaction to take place on, usually as a fine mesh or powder to increase surface area |
What is a benefit of heterogeneous catalysts? | They can be easily separated from the products and leftover reactants |
How can a heterogeneous catalyst be poisoned? | When a substance clings t the surface more strongly than the reactant does, preventing a catalyst from getting involved in the reaction |