Rate Of Reactions Flashcards

1
Q

How can a colorimeter be used to measure rate?

A
  • A colorimeter measures the absorbance of light by a coloured sample.
  • The more concentrated, the darker the colour
  • more light is absorbed.
  • Then plot a calibration curve
  • known concentrations of (iodine) on x-axis.
  • The absorption is measured for sample
  • results are plotted
  • then use curve and absorbance to find out [Iodine]
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2
Q

What is the initial rate?

A

the rate right at the start of the reaction when T=0

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3
Q

Describe a clock reaction

A
  • You time how long it takes for a reaction to occur
  • is used to simplify the initial rate method
  • sit the reaction vessel on a paper with a cross
  • Time how long is takes until you cant see the cross through the beaker
  • There is a colour change
  • This is the end point
  • The quicker the clock reaction, the faster the initial rate is
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4
Q

What are 3 assumptions of the clock experiments?

A
  • Temperature of the reaction remains constant
  • no significant change in conc of reactants during the reaction
  • Reaction has not proceeded too far when the end point is seen.
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5
Q

Describe the iodine clock experiment

A
  • Add sodium thiosulfate and starch (indicator) to excess hydrogen peroxide + iodide ions in sol
  • H2O2 + 2I- + 2H+ = 2H20 + I2
  • Sodium thiosulfate reacts immediately with the Iodine produced
  • 2S2O3(2-) + I2 = 2I- + S4O6(2-)
  • iodine from first reaction used up in second
  • when ST used up, some iodine left in solution
  • starch indicator = blue/black
  • end of clock reaction
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6
Q

What is an order?

A
  • An order is the power to which a concentration is raised to in the rate equation
  • Tells us how the concentration of the substance affects the rate
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7
Q

What is zero order on a rate-conc graph?

A
  • Changes in concentration has no effect on rate
  • If [A] doubles then rate doesn’t change .
  • produces a horizontal straight line with no gradient
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8
Q

What is first order on a rate-conc graph?

A
  • Changes in concentration has a proportional change to rate
  • If [A] doubles then rate doubles.
  • A positive line passing through the origin.
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9
Q

What is second order on a rate-conc graph?

A
  • Changes in concentration has a squared proportional change on rate.
  • If [A] double then rate x4
  • Forms an exponential curve
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10
Q

How to get rate from second order graph?

A
  • Rate-conc graph is a curve
  • Plot a second graph of rate against the conc squared.
  • Results in a straight line through the origin.
  • The gradient of the straight line is equal to the rate constant k.
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11
Q

What does the value of ‘k’ link to rate mean?

A
  • Larger the value of ‘k’ the faster the rate of reaction
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12
Q

Describe zero order on a rate-time graph

A
  • straight line with a negative gradient
  • reaction rate doesn’t change during the reaction
  • gradient = k
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13
Q

Describe first order on a rate-time graph

A
  • downward curve with a decreasing gradient
  • time for the conc of the reactant to halve is constant
  • half life = k
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14
Q

Describe second order on a rate-time graph

A
  • downward curve like 1st

- a lot steeper at the start.

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15
Q

What is half life?

A
  • time taken for half of a reactant to be used up.
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16
Q

How to calculate k for a first order reaction?

A

k = ln2 / t(1/2)

17
Q

what is the rate determining step?

A
  • the slowest step in a multi-step reaction.

- substances that aren’t in the rate equation can’t be in the rate determining step.

18
Q

What is the arrhenius equation?

A
k = Ae^-Ea/RT
k = rate constant 
Ea = activation energy (J mol -1) 
T = temperature (K) 
R = gas constant (8.31) 
A = pre exponential factor
19
Q

What is the relationship between Ea and k?

A
  • As Ea gets smaller, k gets bigger.
  • Bc as Ea drops, ROR increases as particles have enough energy to react when they collide.
  • large Ea = slow rate
20
Q

Effect of increase in temp on k?

A
  • Increase in temperature, increases k
  • particles have more kinetic energy
    more likely to collide with at least the Ea
  • ROR increases.
21
Q

What is the log version of the Arrhenius equation

A
lnk = lnA - Ea / RT
Ea = (lnA - lnk) x RT
22
Q

How to use Arrhenius equation when given T and k table?

A

-Ea/R = gradient
lnA = y intercept
- first convert to 1/T and lnk using values in the table.
- Plot a graph of lnk(y) against 1/T(x)
- calculate the Ea/R from the -gradient of the straight line
- calc Ea by multiplying -gradient by R(8.31)
- Calculate lnA by extrapolating your line back to T=0/y - intercept.
- To calculate A use inverse of ln = e^lnA

23
Q

what is ROR

- ways to measure

A
  • change in the amount of reactants/products per unit time
  • measure volume of gas given off
  • measure loss in mass as gas is evolved
  • colorimetry to measure colour change of a Rt
  • pH change of a reaction