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?

A

No effect

22
Q

Ka units

A

mol/dm3

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
Q

Ka equation

A

Ka=[H+][A-]
[HA]
If it’s a weak acid, it will be [H+]^2

26
Q

Kw units

A

mol2/dm6

27
Q

What can affect Kw?

A

Temperature

28
Q

Buffers equation

A

[H+]=Ka[HA]
[A-]

[A-]= the salt
[HA]= the acid
29
Q

How does adding acid affect buffers?

A
  • 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
Q

How does adding a base affect buffers?

A
  • 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
Q

Indicators

A

Methyl orange- low pH
Bromothymol blue- medium pH
Phenolphthalein- high pH

32
Q

Indicator for both strong acid and base

A

Any indicator

33
Q

Indicator for strong acid-weak base

A

methyl orange

34
Q

Indicator for weak acid-strong base

A

phenolphthalein

35
Q

Indicator for both weak acid and base

A

No indicator