Chapter 5-Chemical Kinetics Flashcards

1
Q

Positive versus negative Gibbs free energy

A

Positive signifies a nonspontaneous reaction.

Negative Gibbs free energy signifies a spontaneous reaction.

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2
Q

Intermediates

A

Molecules that exist within the course of a reaction but are neither reactants and products overall

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3
Q

What is the slowest step of a reaction that limits the maximum rate at which a reaction can proceed?

A

Rate determining step

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4
Q

Collision theory

A

States that her reaction rate is proportional to the number of effective collisions between the reacting molecules.

Arrhenius equation

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5
Q

What two things must occur in order for a reaction to exceed the activation energy?

A

Molecules must be in the proper orientation.

Molecules must have sufficient kinetic energy.

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6
Q

Transition state theory

A

Molecules form a transition state or activated complex during a reaction in which old bonds are partially dissociated and new bonds are partially formed.

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7
Q

Which part of the reaction is the highest point on a free energy reaction diagram?

A

The transition state

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8
Q

In what different ways can you impact reaction rates?

A

1) Increasing the concentration of a reactant. (Increases reaction rate except for zero order rxns)
2) Increasing the temperature of a reaction. (Increases reaction rate because the kinetic energy is increased)
3) Changing a medium can increase or decrease reaction rate depending how the reactants interact with the medium
4) Adding a catalyst increases reaction rate lowers activation energy.

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9
Q

Homogeneous catalyst versus heterogeneous catalyst

A

Homogeneous catalyst are the same phase as the reactants. Heterogeneous catalyst are in a different phase than the reactants.

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10
Q

How are rate laws determined?

A

Rate laws must be determined by experimental data.

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11
Q

Zero order reaction

How is it determined?

A

Have a constant rate that does NOT depend on the concentration of the reactant.

Can only be affected by changing the temperature adding a catalyst.

Concentration versus rate graph line is horizontal.
Slope -k

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12
Q

First order reactions

A

Have nonconstant rates that depends on the concentration of a reactant.

On a concentration versus rate graph line is diagonal

Slope -k

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13
Q

Second order reaction

A

Non-constant rate dependent on the concentration of reaction

concentration vs time curve: parabolic

slope=k

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14
Q

Mixed order reactions

A

Reactions with rate orders that either vary over the course of the reaction or have non-integer orders (fractions)

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15
Q

Broken order reactions

A

Reactions with rate orders that have non-integer orders (fractions)

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16
Q

Optimal temperature range for enzymatic reactions

A

35-40 degrees celsius

17
Q

Units for rate

A

mol/L . s

M/s

18
Q

rate law equation

A

rate=k[A]^x[B]^y

19
Q

Collision theory equation

A

rate= Z x f

Z= total number of collisions per second

f= fraction of collisions that are effective

Simple equation

20
Q

Radioactive Decay

A

[A]t=[A]0 e^-kt

At vs A0 initial concentration of A vs concentration at certain time

k: rate constant