5.1.1 - How Far? Flashcards

1
Q

define rate as an equation

A

change in concentration/ change in time

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2
Q

what are the units for rate

A

mol dm-3 s-1

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3
Q

what is an order of reaction

A

how changing the concentration of a species affects rate

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4
Q

zero order

A

rate ∝ [A]^0

(conc. A has no effect on rate)

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5
Q

first order

A

rate ∝ [A]

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6
Q

second order

A

rate ∝ [A]^2

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7
Q

how to calculate the overall order of a reaction

A

add up the orders of all the reactants in the equation

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8
Q

rate equation (general form)

A

rate = k[A]^m[B]^n

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9
Q

concentration time graph: zero order

A

straight line, negative gradient
gradient = k

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10
Q

concentration time graph: first order

A

decreasing gradient with a constant half life
gradient = rate (can be used to find k)

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11
Q

define half life (t1/2)

A

the time taken for concentration to half

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12
Q

concentration time graph:
equation for finding k, using the half life of a 1st order reaction

A

k = (ln2)/half life

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13
Q

concentration time graph: second order

A

steep decreasing gradient with no constant half life

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14
Q

examples of continuous monitoring methods

A

change in mass, gas volume, colorimetry

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15
Q

rate concentration graph: zero order

A

horizontal line, gradient = 0, rate = k

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16
Q

rate concentration graph: first order

A

straight line graph through origin
positive gradient, rate = k[A]

17
Q

rate concentration graph: second order

A

exponential through origin
k = gradient of conc^2/rate graph

18
Q

why are many reactions multi-step

A

collisions of many moles is very unlikely
if species have the same charge

19
Q

define reaction mechanism

A

the series of steps that make up an overall reaction

20
Q

define rate determining step

A

the slowest step in a multi-step reaction

21
Q

about the rate determining step

A
  • rate equation only includes species of RDS
  • orders in rate equation match the number of species in the RDS
22
Q

what factors mean increasing temperature increases k

A
  • more particles exceed Ea
  • kinetic energy of particles increases so frequency of collisions increases
23
Q

why is increased Ea more significant than increased collisions

A

increases collisions is small in comparison to having more particles over Ea

24
Q

arrhenius equation

A

k = Ae^(-Ea/RT)

25
Q

logged arrhenius equation

A

lnK = (-Ea/R)*(1/T) + lnA