5.3 Flashcards

1
Q

Le Chatelier’s Principle

A

-pressure/volume
-concentration
-temperature

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2
Q

• Changes in temperature

A

pressure and concentration affect

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3
Q

equilibrium (in different ways).

A
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4
Q

•These factors will make the system undergo an equilibrium

A
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5
Q

shift (i.e. the movement of a system at equilibrium

A

resulting

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6
Q

in a change in the concentrations of reactants and products)

A
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7
Q

•The outcome is governed by LE CHATELIER’S PRINCIPLE:

A
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8
Q

•”..when a chemical system at equilibrium is disturbed by a

A
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9
Q

change in a property

A

the system adjusts in a way that

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10
Q

OPPOSES the change.”

A
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11
Q

• Any change to a chemical reaction at equilibrium causes the

A
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12
Q

reaction to proceed in the direction that REDUCES the effect

A
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13
Q

of the change.

A
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14
Q

Le Chatelier’s Principle & Concentration Changes

A
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15
Q

Addition of a reactant

A
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16
Q

or product causes the

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17
Q

reaction to proceed in

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18
Q

the direction that

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19
Q

consumes the added

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20
Q

substance.

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21
Q

Removal of a reactant

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22
Q

or product causes the

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23
Q

reaction to proceed in

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24
Q

the direction that

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25
Q

produces the missing

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26
Q

substance.

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27
Q

Concentration (M)

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28
Q

co

A
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29
Q

3

A
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30
Q

•2503(8)

A
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31
Q

2

A
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32
Q

Concentration Changes

A
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33
Q

1

A
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34
Q

Initial

A
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35
Q

equilibrium

A
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36
Q

(aq)

A
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37
Q

H-

A
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38
Q

NH3

A
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39
Q

N2

A
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40
Q

Nɔ added at

A
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41
Q

+ HCO

A
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42
Q

this time i

A
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43
Q

Nz(0) + 3H2(a) 2NH3(a) Time

A
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44
Q

•CO2 g) t 2H

A

0

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45
Q

increase in acidity [H

A

0”] will cause increase in

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46
Q

3 (ag)

A
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47
Q

New

A
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48
Q

equilibrium

A
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49
Q

H2

A
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50
Q

NH3

A
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51
Q

N

A
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52
Q

ONCSSM 2002

A
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53
Q
  • increase in SO
A

drives reaction to favour production

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54
Q

of S0

A

and O

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55
Q

Concentration Changes:

A
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56
Q

Explanation Based on Kinetic Theory

A
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57
Q

•reactant added = more frequent collisions =

58
Q

increase in rate of forward reaction

59
Q

•rate for reverse reaction does not increase

60
Q

immediately

A

therefore forward and reverse rates

61
Q

are not equal

62
Q

•rate of reverse reaction eventually increases as

63
Q

more product is formed

64
Q

Le Chatelier’s Principle & Temperature Change

65
Q

•Heat evolves in an exothermic reaction and is absorbed in an

66
Q

endothermic reaction.

67
Q

• Changes in temperature have the same effect as changes in

68
Q

concentration

69
Q

Example:

70
Q

• If the mixture is heated

A

the equilibrium shifts toward NO.

71
Q

•If the mixture is cooled

A

the equilibrium shifts toward N

72
Q

• favours exothermic reaction

73
Q

NOTE: the value of the equilibrium constant changes

74
Q

equilibrium constant is only constant at a specific

75
Q

temperature.

76
Q

Temperature Change:

77
Q

• favours endothermic reaction

78
Q

Explanation Based on Kinetic Theory

79
Q

Le Chatelier’

80
Q

a) Cooling an exothermic reaction

81
Q

Nz(g) + O

A

(o) t 180.5 kJ = 2NO

82
Q

uces the missing

83
Q

Concentrabor

84
Q

• Thse facxzwil make tre sste nd:rg3 En squlibeiun

85
Q

(A + B C+ energy)

86
Q

inges

87
Q

forward and reverse reaction rates are slower

88
Q

raverse rate decreases more (requires heat but less heat available)

89
Q

pre

A

more products and more energy will be formed

90
Q

the right (towards products)

91
Q

em tequlitbrhm

92
Q

rinciple & Concentratlon Changes

93
Q

afs

A

irtars rrartian ta fn

94
Q

endothermic reaction

95
Q

+ energy B+ C)

96
Q

ard rate decreases more (requires heat but less heat available)

97
Q

fore

A

more reactants and energy will be formed

98
Q

to the left (towards reactants)

99
Q

hermic and endothermic reactions (=

100
Q

respectively).

101
Q

Le Chatelier’s Principle & Volume/Pressure Changes

102
Q

• only for gaseous equilibria.

103
Q

• decrease in volume (or an increase in pressure) causes

104
Q

reaction to proceed in the direction of fewer number of

105
Q

moles of gaseous reactant or product. These occupy a

106
Q

smaller volume

A

thus relieving the stress of the added

107
Q

pressure on the system.

108
Q

•an increase in volume or a decrease in pressure causes the

109
Q

reaction to proceed in the direction of greater number of

110
Q

moles of gaseous reactant or product.

111
Q

Example: N

A

O4(e2NO2 (e)

112
Q

increase in volume drives the reaction to the right

113
Q

decrease in volume drives the reaction to the left

114
Q

Volume/Pressure Changes:

115
Q

Explanation Based on Kinetic Theory

116
Q

decrease in volume = increase in # of collisions

117
Q

.. increase in forward and reverse reaction rates

118
Q

• rate of forward reaction increases more

119
Q

.” more particles

120
Q

• leads to the production of more products

121
Q

Note: the opposite is true if volume increases

122
Q

250

A

( t Oz (a 250a (e)

123
Q

Changes that DO NOT affect position of

124
Q

equilibrium systems:

125
Q

Adding Catalysts

126
Q

increases the rate of reaction but does not affect the final

127
Q

citin of equilibrium.

128
Q

Concentrallian crasie heor

129
Q

B ot fonart reartion

130
Q

iediately

A

therefere lor vtard everse rate

131
Q
  • rate of reverse reaction gventually ngreases zx.
132
Q

vation energy for both forward and re

133
Q

inert gas at constant volume

134
Q

9-10/12

135
Q

the pressure by adding another gas. If this gas is

136
Q

react with any of the gases (ie. inert) there will be no

137
Q

equilibrium

A

because it doesn’t affect the

138
Q

ions.

139
Q

finert aas chanaes nrobability of effective collisions

140
Q

qually.