General Chemistry Ch 5. Chemical Kinetics Flashcards

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1
Q

Gibbs Free Energy

A

Determines whether or not a reaction is spontaneous

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2
Q

Chemical mechanisms

A

Propose a series of steps that make up the overall reaction

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3
Q

Intermediates

A

Molecules that exist within the course of a reaction but are neither reactants nor products overall

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4
Q

Rate-determining step

A

Limits the maximum rate at which the reaction can proceed, the slowest step

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5
Q

Collision theory

A

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

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6
Q

Activation energy

A

Proper orientation and sufficient Kinect energy must be there for a collision to be effective

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7
Q

Arrhenius equation

A

Mathematical way of representing collision theory

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8
Q

Transition state theory

A

States that molecules from a transition state or activated complex during a reaction in which the old bonds are partially dissociated and the new bonds are partially formed

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9
Q

Transition state

A

Highest point on a free energy reaction diagram, the reaction can proceed toward products or revert back to reactants

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10
Q

Activated complex

A

-

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11
Q

Increasing reactant concentration reaction rate

A

Will increase reaction rate (except for zero-order reactions) because there are more effective collisions per time

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12
Q

Increasing temperature reaction rate

A

Will increase the temperature because the particles kinetic energy is increased

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13
Q

Changing the medium reaction rate

A

Can either increase or decrease the reaction rate depending on how the reactants interact with the medium

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14
Q

Adding a catalyst reaction rate

A

Increases reaction rate because it lowers the activation energy, can either be homogeneous or heterogeneous

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15
Q

Homogeneous catalysts

A

In the same phase as the reactants

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16
Q

Heterogeneous catalysts

A

In a different phase than the reactants

17
Q

Reaction rate measurements

A

Measured in terms of the rate of disappearance of a reactant or appearance of a product

18
Q

Rate laws

A

Take the form of rate = k[A]^x[B]^y, must be determined from experimental data

19
Q

Rate orders

A

Do not usually match the stoichiometric coefficients, the sum of all individual rate orders in the rate law

20
Q

Zero order reactions

A

Have a constant rate that does not depend on the concentration of the reactant, rate can be changed only by changing the temp or adding a catalyst, concentration vs time curve is a straight line with a slope that equals -k

21
Q

First order reactions

A

Have a non constant rate that depends on the concentration of reactant, concentration vs time curve is nonlinear, slope of ln[A] vs time is -k

22
Q

Second order reactions

A

Have a non constant rate that depends on the concentration of reactant, concentration vs time curve is nonlinear, slop of 1/[A] vs time is k

23
Q

Broken-order reactions

A

Those with noninteger orders

24
Q

Mixed-order reactions

A

Those that have a rate order that changes over time