Lesson 16.1.4
16.1.4 Reaction mechanisms and the rate-determining step Quiz: Pearson Edexcel Chemistry, Unit 16
20 questions
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Lesson 16.1.4, Reaction mechanisms and the rate-determining step: 20 multiple choice questions for the Pearson Edexcel Chemistry (9CH0), Unit 16: Kinetics II, written with Revision Ninja.
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The 20 questions
-
What is a rate-determining step?
- The step that produces the final product of the overall equation
- The fastest step in a mechanism, which uses up all the intermediates
- The first step in a reaction mechanism, which always involves a catalyst
- The slowest step in a reaction mechanism, which controls the overall rate of the reaction
-
Which species can appear in the rate equation?
- Only the reactant that has the largest stoichiometric coefficient
- Only intermediates formed in the fast steps after the rate-determining step
- Only the products of the overall reaction
- Reactants and any catalyst involved in the rate-determining step or in steps before it
-
Why can an intermediate not appear in the overall rate equation?
- It is made and used up within the mechanism, so it is not a reactant in the overall equation
- It is formed after the rate-determining step, so it cannot affect the rate of the overall reaction at all
- It is always a gas, so it escapes from the reaction vessel before the concentration can be measured
- It is only present in the products at the end, so it cannot react with any other species in the mixture
-
In the acid-catalysed iodination of propanone, what is the order with respect to iodine?
- 0
- 2
- 1
- -1
-
What is the order with respect to H+ in the acid-catalysed iodination of propanone?
- 1/2
- 2
- 0
- 1
-
Which halogenoalkane hydrolysis has the rate equation rate = k[halogenoalkane]?
- SN2 hydrolysis of a secondary halogenoalkane, where the rate depends on two reactants
- SN2 hydrolysis of a tertiary halogenoalkane, where the rate depends on the hydroxide ion
- SN1 hydrolysis of a tertiary halogenoalkane, where the rate depends only on the halogenoalkane
- SN2 hydrolysis of a primary halogenoalkane, where the rate depends on the hydroxide ion
-
For 2NO + O2 -> 2NO2 with rate = k[NO]^2[O2], what is the overall order?
- 1
- 3
- 2
- 4
-
A mechanism has step 1 (slow): A + B -> X, and step 2 (fast): X + C -> D. Which rate equation is consistent?
- rate = k[A][B][C]
- rate = k[A][B]
- rate = k[X][C]
- rate = k[D]
-
A rate equation is rate = k[NO2]^2 for the overall reaction 2NO2 -> N2O4. Which description of the rate-determining step fits?
- The rate-determining step involves N2O4, which is the product of the reaction
- Termolecular: three NO2 molecules collide in the rate-determining step
- Bimolecular: two NO2 molecules collide in the rate-determining step
- Unimolecular: one NO2 molecule decomposes in the rate-determining step
-
The overall equation is 2A + B -> C and experiments show rate = k[A]^2. Which conclusion about the rate-determining step is best?
- The rate-determining step involves two molecules of A and no B
- The rate-determining step involves only the product C
- The rate-determining step involves one molecule of A and one molecule of B
- The rate-determining step involves one molecule of B and one molecule of A
-
For SN2 hydrolysis of a primary halogenoalkane in a single step, which rate equation applies?
- rate = k[halogenoalkane]
- rate = k[OH-]
- rate = k[halogenoalkane]^2
- rate = k[halogenoalkane][OH-]
-
In the SN1 mechanism, which species is involved in the slow rate-determining step?
- The carbocation and the hydroxide ion, which react in the slowest step
- Only the halogenoalkane, which breaks down to form a carbocation and a halide ion
- The halogenoalkane and hydroxide ions colliding together
- Only the hydroxide ion, which attacks the carbocation
-
A reaction profile shows several steps. Which step is usually the rate-determining step?
- The step with the lowest activation energy, since it is the fastest step
- The step with the highest activation energy, since it is the slowest step
- The step that releases the most energy, since it controls the rate
- The final step that forms the overall products of the equation
-
When does a catalyst appear in the rate equation?
- When the catalyst takes part in the rate-determining step or in a step before it
- When the catalyst is present in the overall equation as a reactant
- When the catalyst is added in a large excess compared with the reactants
- When the catalyst is a solid that is not in the same phase as the reactants
-
Why does the overall stoichiometric equation not always predict the rate equation?
- Catalysts always change the stoichiometry of the reaction
- The rate equation is always determined by the products rather than the reactants
- Rate depends on the slowest step, which may involve fewer or different species than the overall equation
- Rate always depends on the total number of moles of reactants in the balanced equation
-
In the acid-catalysed iodination of propanone, the rate does not depend on [I2]. What does this indicate?
- I2 is the only reactant that controls the speed of the enol formation in the first and slowest step
- I2 is not involved in the rate-determining step, so it reacts in a later fast step
- I2 forms an intermediate that is itself the rate-determining species in the first and slowest step
- I2 is the catalyst, so it appears in the overall equation twice and is regenerated at the end
-
A rate equation is rate = k[NO]^2[H2]. Which mechanism is consistent with this and the overall equation 2NO + 2H2 -> N2 + 2H2O?
- Step 1 (slow): H2 + H2 -> H4; Step 2 (fast): H4 + 2NO -> N2 + 2H2O
- Step 1 (slow): NO + H2 -> N2O + H2O; Step 2 (fast): NO + H2 -> N2 + H2O
- Step 1 (slow): 2NO + 2H2 -> N2 + 2H2O, with no intermediate formed
- Step 1 (slow): 2NO + H2 -> N2O + H2O; Step 2 (fast): N2O + H2 -> N2 + H2O
-
Doubling [OH-] has no effect on the rate of hydrolysis of 2-bromo-2-methylpropane. What does this suggest?
- The reaction is catalysed by hydroxide ions, which are regenerated at the end
- The reaction has a termolecular rate-determining step involving two hydroxide ions
- The reaction is SN1, since the rate-determining step involves only the halogenoalkane
- The reaction is SN2, since hydroxide ions attack in the rate-determining step
-
Rate = k[A][B]^2 is observed. Which two-step mechanism is most consistent with this rate equation?
- Step 1 (slow): A + B -> X; Step 2 (fast): X + B -> products
- Step 1 (slow): A + B + B -> products, in a single termolecular step
- Step 1 (fast): A + B -> X; Step 2 (slow): X + A -> products
- Step 1 (fast equilibrium): B + B <=> B2; Step 2 (slow): B2 + A -> products
-
In a reaction mechanism, what is an intermediate?
- A catalyst that is regenerated at the end of every step and is never used up in the mechanism
- A species formed in one step of the mechanism and consumed in a later step
- A species that appears in the overall equation as a product formed in the final step of the mechanism
- A reactant that is in excess and is never consumed in any step of the reaction mechanism
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