Topic 18: Kinetics Flashcards

1
Q

Rate of reaction at particular instant

A

rate = change in conc. / time

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2
Q

The order of a reaction (with respect to a species)

A

The power to which the conc. of that species is raised in the rate expression.

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3
Q

The overall rate of a reaction

A

The sum of all the orders of reaction in the rate expression.

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4
Q

Units for rate

A

mol dm−³ s−¹

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5
Q

How do you determine rate from conc-time graph?

A

Draw a tangents at different point these determine the rates at certain points of the reaction.

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6
Q

Determining order of a reaction from rate-conc. graphs

A

zero order- horizontal straight line
1st order - straight line through the origin
2nd order - wont be a straight line, plot rate against [X]^2 if straight line, order 2

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7
Q

Using initial rate to determine order with respect to each species.

A

As initial conc of species is *2 if order 2 rate will *2^2. If initial conc of species is *3 rate will *3^3 if order 2.

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8
Q

General rule for increase in temp and rate of reaction.

A

As temp increases by 10K, rate of reaction doubles.

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9
Q

What is the effect of increasing the temperature on k (the rate constant)?

A

Increasing the temperature increases the rate constant.
As you increase the temperature more particles have energy greater than or equal to the activation energy.
So increased frequency of successful collisions.

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10
Q

The Arrhenius Equation

A

​k =Ae^(-Ea/RT)

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11
Q

A in the Arrhenius equation

A

A pre-exponential factor, the frequency of correctly oriented collisions.

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12
Q

Ea

A

Activation Energy is the minimum amount of energy particles require in order for a successful collision to occur causing the reaction to happen.

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13
Q

R

A

The gas constant (usually 8.31)

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14
Q

e^(-Ea/RT)

A

The fraction of collisions with enough energy to react.

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15
Q

Unit for T in Arrhenius equation

A

K

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16
Q

Unit for -Ea in Arrhenius equation

A

Jmol^-1

17
Q

Unit for R in Arrhenius equation

A

JK^-1mol^-1

18
Q

Log form of Arrhenius equation

A

lnk=ln(Ae^(−Ea/RT))
= (−Ea/R)(1/T)+lnA
y=mx+c

19
Q

How to use the log form of the Arrhenius equation

A

Drawing a graph of 1/T and lnk, the gradient will be (-Ea/R) and can be used to determine the activation energy.

20
Q

Rate Determining Step

A

The slowest step in the reaction so it determines the overall rate.

21
Q

Anything _____ the rate determining step wont affect the rate.

A

After, these will be quick in comparison and not affect the rate or be in the rate equation, steps before will potentially be.

22
Q

Determining the rate determining step

A

Either the slowest, the has the reactants in the rate expression, the number of those reactants add to their respective order.
a+b=c
b+c=d
d+c=e
rate equation = k[a][b]^2
step 2 is the rate determining step.

23
Q

The iodine clock reaction step 1

A

H202(aq)+2I-(aq)+2H+(aq) —-> I2(2)+2H20(l) rate determining step (hydrogen peroxide) (potassium iodide)(sulfuric acid)

24
Q

The iodine clock reaction step 2

A

I2(aq) +2S203^-2(aq)——> S406^-2(aq)+2I-(aq) (sodium thiosulfate) (tetrathionate) Excess iodine will react with the added starch and

25
Q

How does the iodine clock reaction work?

A

Step 1 then Step 2. Excess iodine will react with the added starch and turn it from colourless and clear to blue black. Time it with varying conc. of H202.