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Arrhenius Equation

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(1)

Arrhenius Equation

Svante Arrhenius developed a mathematical relationship between k and E a :

where A is the frequency factor, a number that represents

the likelihood that collisions would occur with the proper

orientation for reaction.

(2)

Arrhenius Equation

Taking the natural logarithm of both sides, the equation becomes

When k is determined experimentally at several temperatures, E a

can be calculated from the slope of a plot of ln k vs. 1/T.

(3)

Arrhenius Equation

• This is how the rate constant of a chemical reaction varies with respect to temperature and other variables.

ln(k) = - E a /R(1/T) + ln(A)

where... k= rate constant

E

a

= Activation Energy (in kJ/mole) R = Gas Constant

T = Kelvin temperature

A = “Frequency Factor”-- a constant indicating

how many collisions have the correct

orientation to lead to products.

(4)

• Temperature is defined as a measure of the average

kinetic energy of the molecules in a sample.

• At any temperature there is a wide distribution of kinetic energies.

- A Maxwell-Boltzmann distribution curve/graph shows how the energy was spread out over different molecules

- The area under the curve = the total molecules in the sample, and it doesn’t change

Maxwell-Boltzmann Distribution

(5)

Maxwell–Boltzmann Distributions

• As the temperature increases, the curve flattens and broadens.

• Thus at higher temperatures, a larger population of molecules

has higher energy.

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