Rates Flashcards

(34 cards)

1
Q

Give a basic definition of rate of reaction.

A

Rate = change in concentration / time

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2
Q

What are the units of rate of reaction?

A

mol dm-3 s-1

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3
Q

How might we measure rates practically? (x5)

A
  • Change in mass
  • pH measurement
  • Colorimetry
  • Chemical analysis: titration with quenching to stop the reaction’s progression
  • Production of a solid precipitate
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4
Q

What factors affect rate of reaction? (x4)

A
  • Concentration
  • Temperature
  • Presence of a catalyst
  • Surface area of solid reactants
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5
Q

How can we explain the effect of concentration on the rate of reaction, using collision theory?

A
  • More particles per unit volume
  • Effective collisions occur more frequently
  • Increase in rate
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6
Q

What are the two axes of a Maxwell-Boltzmann distribution graph?

A

X-axis: energy, E
Y-axis: number of particles

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7
Q

What does the area beneath a Maxwell-Boltzmann distribution represent?

A

The total number of particles in a given system.

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7
Q

Describe the basic features of a Maxwell-Boltzmann distribution.

A
  • Asymmetrical bell curve
  • The graph starts at the origin; no particles have E=0
  • The graph never reaches the x-axis beyond this, as there is no maximum energy carried by a given particle
  • The peak of the curve represents the most probably energy of particles E(mp)
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8
Q

How would a higher temperature affect the Boltzmann distribution?

A

E(mp) will shift to the right, and the height of the distribution curve will decrease to maintain a constant area. The area lying beyond threshold E(a) would increase so more particles collide successfully.

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9
Q

How would the presence of a catalyst affect the Boltzmann distribution?

A

The curve itself wouldn’t change, but the area lying beyond the threshold E(a) would be greater and hence more particles would collide successfully.

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10
Q

How do we use a Maxwell-Boltzmann distribution to explain rate of reaction?

A

We consider how changing an external factor affects the total area of the graph lying beyond the threshold E(a).

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11
Q

Define catalyst.

A

A substance providing an alternative reaction pathway with a lower activation energy.

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12
Q

Explain the difference between heterogeneous and homogeneous catalysts.

A

Heterogeneous - DIFFERENT phase as the reactants.
Homogeneous - SAME phase as the reactants.

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13
Q

How do heterogeneous catalysts work?

A
  • Reactant molecules absorb onto the surface of the catalyst.
  • Bonds in the reactants weaken and break, and new ones are formed.
  • As bonds are weakened, the products now easily resorb away.
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13
Q

What is the most important aspect of catalytic function?

A

The catalyst is fully re-formed at the end of the reaction.

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14
Q

Why might we use a catalyst for a reaction involving multiple negative-charged reactants?

A

The activation energy of this process will be very high as strong e.static forces of attraction need to be overcome. Catalysts work to reduce this activation energy.

15
Q

Explain the significance behind the order of a reactant in a rate equation.

A

The order represent how changing the concentration of a reactant changes the rate of reaction.

16
Q

If a reactant doesn’t feature in the rate equation, how does it affect rate of reaction?

A

It doesn’t - the reaction is zero order wrt. the concentration of this reactant.

17
Q

How do we determine the overall order of a reaction?

A

Sum of all individual reactant orders.

18
Q

What is the rate constant, k?

A

This is a proportionality constant, converting orders and concentrations to rates.

19
Q

How do we determine the units of k?

A

Re-arrange the rate equation to make k the subject.

20
Q

Describe how the shape of a RATE-CONCENTRATION graph relates to order.

A
  • Straight horizontal line: zero order
  • Straight diagonal line: first order
  • Upwards quadratic: second order
21
Q

Describe how the shape of a CONCENTRATION-TIME graph relates to order.

A
  • Straight line: zero order, concentration is independent of rate as gradient is constant
  • Quadratic curve: first order, concentration is proportional to rate as half-life is constant
  • Steeper quadratic curve: second order
21
Q

How can we determine k graphically?

A

With the conc.-time graph for a first-order reactant, divide the natural log of 2 by the half-life t(1/2).

22
Why do reactions typically occur over multiple steps?
It's highly unlikely that >2 reactants will collide at once.
23
What is the rate-determining step of a general reaction mechanism?
The slowest step; the overall rate is dependent on the rate of this step, as the others steps are fast and hence have negligible imppact
24
What species will appear in the rate equation? (x2)
- Catalysts (rate eqtn. only) - Species involve in steps up to and including the RDS
25
How can be determine the nature of the reaction mechanism practically?
- We can determine the rate equation experimentally, this shows the RDS. - This step forms an intermediate for use in the later fast step. - This step uses up remaining reactants from the overall eqtn.
26
How might reactants in a mechanism form an intermediate?
- Adding reactants - Splitting reactants to form a product and an intermediate - Combining reactants to form a product and an intermediate
27
How is the Arrhenius equation written?
k=Ae^(-E(a)/RT) ln k = ln A - E(a)/RT
28
What is the role of the Arrhenius equation?
It links the rate constant k with temperature and the activation energy of a reaction.
29
How does the rate equation describe the rate-determining step?
- Only the species in the rate equation feature in the RDS - The orders of reactants in the rate eqtn. match the number of species in the RDS
30
How can we re-arrange the Arrhenius equation to apply it graphically?
- We know that ln k = ln A - E(a)/RT - This re-arranges as ln k = -E(a)/R * (1/T) - This resembles y=mx+c - The modulus * R=8.314 of a graph of ln k against 1/t is equal to E(a)
30
How can we use the Arrhenius equation to predict changes in rate of reaction?
- We compare values of k under different conditions - We know that k is a factor of proportionality in the rate equation, so if k doubles so will rate.