5.1 Flashcards

1
Q

Overall order

A

Sum of individual orders

Eg. 1st order + 2nd order = 3

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2
Q

Units of K (rate constant)

A

-3 -1

Mol Dm S

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3
Q

Concentration-time graphs: 0 order

A

Straight line slanted downwards

k=ln(2)/half life

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4
Q

Concentration-time graphs: 1st order

A

Normal curved line downwards

k=ln(2)/half life

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5
Q

Concentration-time graphs: 2nd order

A

Steep curved line downwards

k=ln(2)/half life

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6
Q

Half life

A

Help to find the order of a reaction. They are the difference between the 1st half life and 2nd

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7
Q

Finding rate constant from graphs using half life

A

k=ln(2)/half life

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8
Q

Rate-concentration graphs: 0 order

A

Flat straight line

k=rate/concentration (gradient)

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9
Q

Rate-concentration graphs: 1st order

A

Straight line slanted upwards

k=rate/concentration (gradient)

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10
Q

Rate-concentration graphs: 2nd order

A

Curved line upwards

k=rate/concentration (gradient)

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11
Q

Relationship between rate and time

A

Rate is inversely proportional to time

rate=k/t

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12
Q

Clock reaction

A

The time it takes for the colour to change. Then plot the graph 1/t.

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13
Q

Determining rate constant from a graph

A

If it’s first order, k=gradient

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14
Q

How does temperature affect the rate constant?

A

Increase in temperature increases the rate constant (k).This is because more molecules exceed the minimum activation energy so react.

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15
Q

Arrhenius equation

A

-Ea/RT
k=Ae
Used in graphs, with gradient=lnA and y-intercept=-Ea/R

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16
Q

Homogeneous equilibrium

A

All species in the system are in the same state

17
Q

Heterogeneous equilibrium

A

All species in the system are in different states

18
Q

Kc equation

A

[Products]
[Reactants]
-For equilibrium reactions
-If heterogeneous, solids and pure liquidws aren’t included in the equation

19
Q

What are the meanings of the Kc/Kp value if it is less than 1?

A

Equilibrium is to the left

Reactants are favoured

20
Q

What are the meanings of the Kc/Kp value if it is more than 1?

A

Equilibrium is to the right

Products are favoured

21
Q

What is the affect of a catalyst on equilibrium?

22
Q

Ka units

23
Q

What does a large Ka value mean?

A

Lots of dissociation

Acid is strong

24
Q

What does a small Ka value mean?

A

If Small amount of dissociation

Acid is weak

25
Ka equation
Ka=[H+][A-] [HA] If it's a weak acid, it will be [H+]^2
26
Kw units
mol2/dm6
27
What can affect Kw?
Temperature
28
Buffers equation
[H+]=Ka[HA] [A-] ``` [A-]= the salt [HA]= the acid ```
29
How does adding acid affect buffers?
- The salt [A-] decreases because it react with the [H+] - The acid [HA] increases because it is formed - The equilibrium shifts to the left
30
How does adding a base affect buffers?
- The salt [A-] increases because [OH-] reacts with [H+] to make H2O, so more acid dissociates - The acid [HA] decreases - Equilibrium shifts to the right
31
Indicators
Methyl orange- low pH Bromothymol blue- medium pH Phenolphthalein- high pH
32
Indicator for both strong acid and base
Any indicator
33
Indicator for strong acid-weak base
methyl orange
34
Indicator for weak acid-strong base
phenolphthalein
35
Indicator for both weak acid and base
No indicator