Rate equations Flashcards

(23 cards)

1
Q

Iodine Clock Experiment: State and explain why different volumes of water are added to each mixture. MS [2]

A

To make volumes constant for all mixtures.

So that volume of propanone is proportional to concentration.

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2
Q

RP7a: How do we use results from an iodine clock experiment to determine order of reaction with respect to Iodide ions? MS [5]

A

in results, we have time taken to go blue
for different [A]
Rate = 1/t
Plot log 1/t vs log [A]
Gradient = Order of Reaction

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3
Q

What is the difference between a continous rates and an initial rates method?

A

continuous involves following one experiment over time, recording the change in [ ] e.g using gas syringe
whereas initial rates involves timing different experiments to reach a fixed [ ] of product then doing 1/t to work out initial rate

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4
Q

RP7a - Recall what occurs during an Iodine Clock Experiment [9]

Include:
Practical Procedure
Purpose of Thiosulfate
Independent, Dependent, Control Variables

A

KI, H2SO4, Starch and S2O3 all in 1 beaker
H2O2 in a separate beaker
Add H2O2 to the first beaker, then immediately start timer
H2O2 reacts with I- to form I2
Thiosulfate then immediately reacts with Iodine formed
Excess I2 remains after all Thiosulfate is used up
Reaction with starch suddenly forms blue-black colour
[I2] is varied, all others remain constant
In each experiment, time taken for reaction mixture to turn blue is measured

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5
Q

What is meant by order of reaction?

A

Power of concentration term in the rate equation

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6
Q

What does the rate equation show us about a mechanism?

A

shows species which appear in or before the rds

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7
Q

How can you determine for the order of reaction for compound A from the a series of steps in a mechanism?

A

The order of reaction is the number of molecules of that
species involved in or before the rate determining step.

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8
Q

What is the ‘rate-determining step’?

A
  • Each step has a different rate of reaction
  • The slowest step controls the rate of reaction
  • This is called the RDS (rate determining step)
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9
Q

What are the typical units for Activation Energy when calculated from gradient?

A

J mol-1

To conver to kJ / mol, divide by 1000

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10
Q

Zero order

A

Time \
Concentration -

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11
Q

First order

A

Time (
concentration /

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12
Q

Second order

A

Concentration )

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13
Q

What 2 factors does the Arrhenius constant take into consideration

A

frequency of collisions
orientation of molecules

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14
Q

What’s the arrhenius equation

A

K = Ae ^-(Ea/RT)

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15
Q

How can we relate temperature to the rate constant, k?

A

Increasing temperature increases K

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16
Q

Different volumes of the same initial concentrations will have the …

A

same initial rate but endin different amounts

17
Q

Why is it preferable to do rate calculations with the initial rate?

A

To know conc of reactants at the start of the reaction

18
Q

If one reactant is in a muchlarger excess, what is it’s order of reaction?

A
  • Order = 0
  • No change on the rate of reaction
  • Concentration is effectively constant
19
Q

What are the limitations of a typical gas syringe?

A

only 100ml of gas, so you don’t want a reaction to produce more than this volume

20
Q

What is important to note about k the rate constant, regarding temperature?

A
  • k is only constant at a fixed temperature
  • the value of k refers to a specific temperature and it increases if we increase temperature
21
Q

How do we work out total order?

A

add all the individual orders together (m+n+…)

22
Q

What is the generalised rate equation for reaction ‘‘aA + bB→’’?

A

r = K[A]^m[B]^n

23
Q

How do you find Ea with the arrhenius equation?

A

Ea = RT (LnA-LnK)