Kinetics Flashcards

1
Q

Why do most collisions by reactant particles not lead to a reaction?

A
  • Collisions may not have enough energy
  • Particles may not be in the correct orientation when they collide
  • Collisions may not be between the correct particles
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2
Q

What do high and low activation energies mean in terms of rate of reaction?

A

High activation energy means its a slow reaction.
Low activation energy means its a faster reaction.

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3
Q

What is the rate of reaction a measure of?

A

How quickly a reaction happens (i.e its speed)

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4
Q

What is the definition of rate?

A

The change in concentration of a substance per unit time

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5
Q

What are the 4 things the rate can be affected by?

A

Concentration (or pressure with gas)
Surface area (solids)
Temperature
Addition of a catalyst

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6
Q

How does an increase in concentration/ pressure affect the rate?

A

Increasing the concentration/ pressure increases the rate as there are more particles in a given volume so there are more frequent, successful collisions will happen.

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7
Q

How does increasing the surface area affect the rate?

A

Increasing the surface are increases the rate as more particles if the solid are exposed, so there is more chance of a successful collision with a reactant.

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8
Q

How does increasing the temperature affect the rate?

A

Increasing the temperature increases the rate as the particles move faster (collide more often) and there are more particles with energy that is bigger than activation energy

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9
Q

How does adding a catalysts affect the rate of reaction?

A

Adding a catalyst increases the rate as it provides an alternative pathway with a lower activation energy (lowering the activation energy means there are more particles withe energy larger than the activation energy, so there are more successful collisions possible, so the rate increases)

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10
Q

What are the units of k, the rate constant?

A

m^-2dm^6s^-1

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11
Q

Can catalysts appear in the rate equation?

A

Yes

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12
Q

What is the only way rate equations can be derived?

A

Through experiments

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13
Q

What is the arrhenius equation?

A

ln(k) = -Ea/RT +lnA\

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14
Q

What does Zero order look like on a concentration time graph?

A

A straight line showing a constant decline in concentration

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15
Q

What does Zero order look like on a rate concentration graph?

A

Horizontal line (rate does not depend on concentration)

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16
Q

What does First order look like on a concentration - time graph?

A

A slightly sloping curve which drops with a constant half-life

17
Q

What does First order look like on a rate - concentration graph?

A

Sloping line upwards (g=k) as the rate is directly proportional to the concentration

18
Q

What does second order look like on a concentration time graph?

A

The curve declines steeply at first then levels out

19
Q

What does second order look like on a rate concentration graph?

A

A sloping curve uphill

20
Q

What does second order look like on a rate- concentration squared graph

A

A diagonal line sloping upwards. The rate is directly proportional to the concentration squared.

21
Q

What do rate mechanisms describe?

A

The sequence of steps in which reactants are converted into products via short lived intermediate species

22
Q

What is the shortest step in a reaction mechanism and why is it called this?

A

The Rate Determining step (r.d.s) as its the step which controls the overall rate of the whole reaction

23
Q

What is the assumption made to do with the order of a particular reaction?

A

The order with respect to a particular reactant shows the number if particles of it participating before or during the rate determining step

24
Q

What do we presume about a zero order reactant?

A

That it is present in the mechanism only after the r.d.s

25
Q

Halkoalkanes are hydrolysed by hydroxide ions to produce what?

26
Q

For primary haloalkanes the can equation can be shown to be what (Haloalkane = RX)

A

rate = k[RX][OH-]

27
Q

For tertiary haloalkanes the can equation can be shown to be what (Haloalkane = RX)

A

rate= k[RX]