Chemical Kinetics Flashcards

1
Q

Gibbs free energy

A

determines whether or not a reaction will occur by itself without outside assistance

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2
Q

High substrate conditions saturate the active sites of the enzyme,leading to

A

maximal turnover

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3
Q

Reaction intermediates

A
  • does not appear in the overall reaction

- difficult to detect

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4
Q

Rate - determining step

A
  • slowest step in the reaction

- limits the minimum rate at which the reaction can proceed

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5
Q

The rate of the whole reaction is only as fast as the

A

rate determining step

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6
Q

Collision theory of chemical kinetics

A
  • states that the rate of a reaction is proportional to the number of collisions per second between the reacting molecules
  • in order for a reaction to occur, molecules must collide with one another (not all collide, must be in correct orientation and have sufficient kinetic energy to exceed the activation energy)
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7
Q
Activation energy (Ea)
(energy barrier)
A
  • the minimal energy of collision for a reaction to take place
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8
Q

rate of reaction equation

A

rate = Z x f

Z= total # of collisions occurring per second
f = fraction of collision that are effective
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9
Q

Arrhenius equation

A

a mathematical way to represent collision theory

as the frequency factor of the reaction increases, the rate constant of the reaction also increases in a direct relationship

Therefore, rate of a reaction increases with temperature

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10
Q

Transition state theory

A
  • states that molecules form a transition state or activated complex during a reaction
  • has greater energy than products and reactants
  • the point of maximum energy
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11
Q

(+) delta G = (endergonic/exergonic) = (energy absorbed/energy given off)

A

endergonic

energy absorbed

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12
Q

(-) delta G = (endergonic/exergonic) = (energy absorbed/energy given off)

A

exergonic

energy given off

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13
Q

Free energy change of the reaction

delta Grxn

A

the difference between the free energy change and free energy of the reactants

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14
Q

Reaction rates can be affected by:

A
  1. increase the conc. of reactant = increase rxn rate (all but zero-order rxns)
  2. increase the temperature = increase rxn rate
  3. changing the medium = can increase or decrease rxn rate
  4. adding a catalyst = increase rxn rate; lowering activation energy
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15
Q

Homogenous catalysts

A

same phase (solid, liquid or gas) of reactants

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16
Q

Heterogenous catalysts

A

different phase (solid, liquid or gas) of reactants