Rates Flashcards

1
Q

Rate of Reaction definition

A

The change in concentration per unit of time

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2
Q

Why do rate of reactions start of fast but then slow?

A
  • Initially there is a high concentration of reactants so a large frequency of successful collisions.
  • As the reactants start to get used up successful collisions become less frequent.
  • Once one or more reactants are used up the can be zero successful collisions.
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3
Q

conc vs time graphs

A

A + 2B → C

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4
Q

What do different orders mean?

A

Zero order:
changing the concentration of a reactant has no effect on the rate of reaction

1st order:
The rate is directly proportional to the concentration of the reactant e.g. doubling the concentration of the reactant, doubles the rate.

2nd order:
The rate is proportional to the square of the change in concentration e.g. doubling the concentration causes the rate to increase by 4 (2^2)

The overall order is the sum of the orders

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5
Q

What does using a large excess of reactant mean?

A

Using a large excess of a reactant will mean the order of reaction is zero with respect to that reactant as the reactants concentration is effectively constant.

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6
Q

Units of k

A
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7
Q

Continuous Monitoring Method

A

1) By taking samples at regular intervals
2) By using a visible indicator/physical property such as gas volume

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8
Q

How to stop CMM for still reacting

A

To stop the reaction, quench the reaction by adding a large volume of cold distilled water.
This will both cool and dilute the reaction decreasing the rate.

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9
Q

CMM Monitoring using a physical property problem

A

This records the amount of product produced. The order of reaction is about the reactants. The volumes recorded would need converting to reactant concentration.

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10
Q

Concentration time tangent

A

gradient = rate

Straight line = constant = 0 order

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11
Q

Explain how the graph shows it is 0 order

A

as [H+] changes there is a constant gradient so rate stays the same

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12
Q

1st or 2nd order

A
  • draw 1st tangent at t=0
  • draw 2nd tangent at 1/2 initial conc
  • compare increase in rate to conc change
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13
Q

Calculating rates orders

A
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14
Q

Initial Rates Method

A

the time it takes to get to a specific point in the reaction is recorded for each experiment.
For example the time is recorded when 20cm3 of gas are produced or when the mixture changes colour or a precipitate is formed.

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15
Q

The Thiosulphate – Acid Reaction

A

When the total volume is constant in each experiment the volume of the reactant is proportional to its concentration.

Rate = 1/t

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16
Q

The iodine clock reaction

A

S2O3 2- = sodium thiosulfate (slows down colour change of I2 - cannot add last)

  • Measure known volumes of reactants. Keep them separate so the reaction doesn’t start.
  • Measure a known volume of sodium thiosulphate.
  • Start the stop clock when the last of the reactants is added to a conical flask. Do not add sodium thiosulphate last.
  • Stop the timer when the mixture turns blue/black and record.
  • Repeat the experiment using the same total volume altering the volume of KI (see table).
  • Rate = 1/time
  • Plot a graph of 1/t against vol of KI (draw all orders)
17
Q

Initial rates orders

A

1st order conc. proportional to rate

18
Q

Initial rates calculations

A
19
Q

Arrhenius equation

A

ln k = -Ea/R x 1/T + ln a
y = m x + c

20
Q

calculating Ea

A
21
Q

Rate equations and mechanisms

A

THE SPECIES IN THE RATE DETERMINING STEP MUST MATCH THE SPECIES IN THE RATE EQUATION