Rates + Equilibrium Flashcards

(55 cards)

1
Q

rate equation

A

r = K[A][B] etc.

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2
Q

zero order

A

concentration have no effect on the rate

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3
Q

first order

A

rate increases by same factor as concentration increases

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4
Q

second order

A

rate increases by conc increase factor²

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5
Q

rate units

A

mol/dm3/s

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6
Q

half life

A

Time taken for half the reagent to be used up

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7
Q

half life in first order reaction

A

always the same

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8
Q

use of half lives

A

to determine whether or not a reaction is first order

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9
Q

Arrhenius equation shows

A

effect of changing temp/activation energy on the rate constant

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10
Q

Kc equation

A

Kc = [products] / [reactants]

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11
Q

mole fraction equation

A

= moles of gas A \ total moles of gas

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12
Q

partial pressure

A

the pressure one gas would except if it was the only gas in the container

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13
Q

partial pressure equation

A

pp = mol frac. x total pressure

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14
Q

only factor that changes Kc

A

temperature

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15
Q

dynamic equilibrium

A

both the foward and backwards reactions are taking place, at the same rate

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16
Q

dynamic equilibrium

A

both the forwards and backwards reactions are taking place, at the same rate

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17
Q

effect of pressure on position of equilibrium

A

pressure increase = favours the side with fewer gas molecules (reducing pressure of the system)

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18
Q

effect of temperature on position of equilibrium

A

temp increase = favours endothermic reaction

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19
Q

effect of concentration on position of equilibrium

A

conc. increase = favours side with fewer moles

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20
Q

Kc > 1 =

A

equilibrium position is towards PRODUCTS

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21
Q

Kc < 1 =

A

equilibrium position is towards REACTANTS

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22
Q

Kc = 1 =

A

equilibrium is HALFWAY between products and reactants

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23
Q

heterogeneous catalyst

A

catalyst in different phase (state) to reactants

24
Q

homogeneous catalyst

A

catalyst in the same phase (state) as reactants

25
how does a homogeneous catalyst work?
forms intermediate species which react to form products and reform the catalyst
26
how does a heterogeneous catalyst work?
reaction occurs on its surface (therefore bigger SA = faster rate)
27
rate
the change in the amount of reactants or production per unit of time
28
Ea eq.
Ea = RT (ln A- Ln K)
29
Arrhenius equation
K = Ae [to the power or] -(Ea/RT)
30
gas constant
8.31 JK-1mol-1
31
Kp eq.
[products partial pressure] / [reactants partial pressure]
32
3 stages of contact process
1) sulfur solid is melted and combusted with oxygen = sulfur dioxide 2) sulfur trioxide formed from sulfur dioxide (reversible) with vanadium catalyst (exothermic) - 450 degrees C 3) sulfur trioxide reacted with oleum + conc. sulphuric acid (v. exothermic) to make sulphuric acid
33
uses of H2SO4
- drug manufacture - metal treatment - paint - making explosives
34
how do catalysts reduce damage to environment? (2)
- reactions take place at lower activation energy ∴ less fuel used, less CO2 emitted - better atom economy - less hazardous chemicals produced
35
uses of hydrogen? (3)
- fuel cells - Haber process - hydrogenation of alkenes
36
dynamic equilibrium
where the rate of forwards and backwards reactions are the same IN A CLOSED SYSTEM
37
equation for rate constant using half lives
k = ln(2) / half life
38
instantaneous rate
rate when t=0
39
method for determining Kc experimentally
- in conical flask mix substances - add acid catalyst - set up another conical flask with same acid catalyst as control - stopper both flasks - leave for a week so they reach equilibrium - carry out titration using NaOH - repeat titration with control to determine amount of acid catalyst used - analyse to determine eq amounts and concs - use kc equation
40
catalyst
a species which speeds up a reaction w/o undergoing permanent change itself
41
le Chatiliers principle
when a change is imposed on a closed system at equilibria, the position of the equilibrium will shift to minimise the effect of the change
42
temp increase favours
ENDOTHERMIC
43
temp decrease favours
EXOTHERMIC
44
Kc =
[products] / [reactants]
45
Kc > 1 =
eq. towards PRODUCTS
46
Kc < 1 =
eq. towards REACTANTS
47
K =
rate / [A]2
48
methods of continuous rate monitoring (2)
- gas collection | - mass lost
49
K = (using t 1/2)
ln2. /t 1/2
50
effect of temp on Kc - (temp up =)
rate up = Kc UP
51
Kp =
partial pressure (products) / pp. (reactants)
52
conc increase favours...
side producing fewer moles
53
conc decrease favours
side producing more moles
54
if K is negative ..
towards reactants
55
is K is positive ...
towards products