unit 7 Flashcards

(38 cards)

1
Q

can you obtain 100% conversion in a reversible/equilibrium rxn

A

no, will always result in a mixture of reactants and products

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

equilibrium position

A

when forward rxn slows and reverse rxn speeds up until they are taking place at the same rate
- describe the concentration of reactant and product at this point (will be constant but not always equal)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

where can equilibrium be achieved

A
  • only in a closed system (rxn takes place in a seal container)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

macroscopic properties to tell eq’m has been reached (l)->(g)

A
  • liquid level will decrease at first as more particles are becoming gaseous
  • eq’m reached when liquid level stops decreasing (no more change)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

4 condition that apply to all equilibrium systems

A
  • 2 opposing processes are going at an equal rate
  • the system undergoes no observable changes
  • can only exist in closed system
  • eq’m can be achieved from either direction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

dynamic equilibrium

A

where rates of the forward and reverse rxns are equal but the properties/concentrations are constant
- dynamic as reactions are still occuring, at same rate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is the K value affected by

A

temperature

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is not included in an equilibrium constant expression

A
  • don’t included pure solids/liquids in an equilibrium constant expression
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what happens for Kc when you reverse an equation

A
  • it becomes inverted
    R–>P = K
    P–>R = 1/K
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

when you multiply/divide each coefficient in a balanced equation, what happens to Kc

A
  • multiply: raise Kc to corresponding power
  • divide: take corresponding root of Kc
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what happens to the Kc when you combine individual equations

A
  • multiply their Kc to obtain Kc for net reaction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what does a large Kc represent

A
  • extent of rxn
  • reaction that goes almost to completion so high conc. of products
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what does a small Kc represent

A
  • extent of rxn
  • reaction that is incomplete, low conc. of products
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

at what Kc is a rxn most likely to reach eq’m

A

when Kc is neither very large or very small

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what does the reaction quotient represent

A
  • can be used to determine the position of a reaction relative to the final equilibrium at any point in time
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

reaction quotient where there are pure reactants

17
Q

reaction quotient when there are pure products

A

infinity/undefined

18
Q

reaction quotient when there is 1 mol of each species

19
Q

how can the reaction quotient determine direction of rxn

A
  • if Q=Kc, at equilibrium
  • if Q<Kc, rxn proceeds forward to eq’m (left of eq’m)
  • if Q>Kc, rxn proceeds in reverse direction to eq’m (right of eq’m)
20
Q

importance of LeChatelier’s principle

A

to predict the qualitative effects of changes of temp, pressure, and conc. on the position of equilibrium + value of eq’m constant

21
Q

what is lechatelier’s principle

A
  • a system at equilibrium when subjected to a change will respond in a way to minimize the effect of the change
    (what is done to a system at equilibrium, it will respond in the opposite way, est. a new eq’m)
22
Q

how does a rxn shift when a reactant is added/removed

A
  • added: towards the products
  • removed: towards reactant
23
Q

how does a rxn shift when a product is removed

A
  • shifts towards products
24
Q

how does a rxn shift when pressure is increased (or volume decreased)

A
  • shift in direction that produces the least number of molecules
25
how does a rxn shift when pressure is decreased(or volume increased)
- shift in direction that produces greater # of molecules
26
how does a rxn shift when pressure in increased/decreased with no change in # of molecules
- no effect on the equilibrium
27
how does a rxn shift when temp increases/decreases
- inc: an endothermic reaction is favoured - dec: an exothermic reaction is favoured
28
how does a rxn shift when a catalyst is added
- no effect on equilibrium, but does help rxn reach eq'm faster
29
what does graph involving lechatelier look like - temperature changes
- system adjusts gradually to temp change - no sudden changes in conc. of any species so NO VERTICAL LINES on graph
30
what does graph involving lechatelier look like - concentration changes
- when substance is added/take away, a sudden change in conc, ONE VERTICAL LINE on graph - eq'm will shift so new eq'm will never return to what it originally was
31
what does graph involving lechatelier look like - change in pressure
- conc. of every gas in container changes w pressure, ALL SUBSTANCES HAVE VERTICAL LINES before LCP kicks in -
32
gibbs energy in a product favoured reaction
negative (spontaneous in forward direction)
33
gibbs energy in a reactant favoured reaction
positive (spontaneous in reverse direction)
34
gibbs energy graph of product favoured reaction
- parabola that starts higher and ends lower (neg gibbs energy) with the vertex closer to the products side
35
gibbs energy graph of reactant favoured reaction
- parabola that starts lower and ends higher (pos. gibbs energy) with the vertex closer to the reactants side
36
what does the vertex on a gibbs energy graph rep
the equilibrium
37
ΔG vs. ΔGtheta
actual energy change under non-standard condition (changes as reaction proceeds) vs. standard conditions and does not change
38
relationship between ΔGtheta and K
- if ΔGtheta<0, then K>1, eq'm mixture has mostly products - if ΔGtheta>0, then K<1, eq'm mixture has mostly reactants - if ΔGtheta=0, then K=0, eq'm reached (same amount of prods and reactants)