SECTION 5 - KINETICS Flashcards

1
Q

Thermodynamics

A

Tells us how much of a reaction will take place

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2
Q

Kinetics

A

Tells us how fast a reaction will happen

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3
Q

3 main things that influence reaction rate

A
  • Temperature (higher –> faster)
  • Surface area (larger –> faster)
  • Concentration (higher –> faster)
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4
Q

Triangle

A

Change in

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5
Q

Reaction rate

A

Quantitative measure of how fast the reaction proceeds to consume the reactants/produce the products

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6
Q

+ sign

A

Product (appearance)

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7
Q
  • sign
A

Reactants (dissapearence)

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8
Q

Differential rate law

A

Equations that tell us how the instaneous rate changes with reactant concentrations

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9
Q

Rate law

A

K[A]^n relationship between concentration and rate

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10
Q

Zero order

A

Rate is NOT dependant on concentration of reactants k[A]^0 (constant)

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11
Q

First order

A

Rate is dependant on concentration of reactants k[A]^1 (2x)

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12
Q

Second order

A

Rate is dependant on concentration of reactants k[A]^2 (4x)

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13
Q

Units of k

A
  • Zero order: M L s-1
  • First order: s-1
  • Second order: L M -1 s -1
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14
Q

Multiple reactant reaction

A

The overall order becomes the sum of the reactant exponents

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15
Q

Integrated rate law

A

Relationship between concentration and time

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16
Q

What do we do with minutes in integrated rate law

A

Convert to seconds

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17
Q

Half life (t1/2)

A

The time it takes for one half of a given amount of reactant to be consumed (time used to use half of reactant)

18
Q

Collision theory

A

Tells us that the reactant particles (ion/atom/molecule) must collide in order to reactant (higher reactant concentration = higher probability of success)

19
Q

Postulates of collision theory

A
  1. Reaction rate is proportional to the number of reactant collisions
  2. Reactants must be properly oriented when they collide for reaction to occur
  3. Reactants must have kinetic energy when colliding
20
Q

Activation energy

A

Minimum amount of energy needed for molecules to collide for reaction to occur

21
Q

Vertical axis of activation energy diagram

A

Potential energy (P.E), enthalpy (H), Gibbs energy (G)

22
Q

Horizontal axis of activation energy diagram

A

Time

23
Q

-H

A

Exothermic (release heat)

24
Q

+H

A

Endothermic (absorb heat)

25
Q

Transition state

A

Top of the energy curve

26
Q

Arrhenius equation

A

Relates raw and temperature k=Ae^ -Ea/RT

27
Q

A

A

Frequency factor (how often correct collisions occur)

28
Q

e^

A

exponential factor (describes temperature effect on K)

29
Q

R

A

Universal gas constant 8.314 J K-1 mol-1

30
Q

T

A

Temperature in Kelvins

31
Q

Ea

A

Activation energy

32
Q

If Ea increases

A

e^-x decrease, k decrease, rate decrease

33
Q

If Ea decreases

A

e^-x increase, k increase, rate increase

34
Q

If K increase

A

e^smaller number, k increase, T increase, k increase

35
Q

Reaction mechanism

A

Series of steps by which an overall chemical reaction occurs

36
Q

Elementary steps

A

Term for the individual steps in reaction mechanism

37
Q

Catalysts

A

Increase rate of reaction by decreasing activation energy

38
Q

Homogenous catalysts

A

Same phase/state as reactants

39
Q

Heterogenous catalysts

A

Different phase/state as reactants

40
Q

Enzymes

A

Catalysts in biological systems

41
Q

Substrate

A

Active sites on enzymes that hold reactants substrate

42
Q

Maud Menten & Leonor Michaels

A

First described single substrate enzyme reactions