rate=
change in conc/ time
zero order
first order
second order
the rate equation
rate= k [A]m [B}n (m & n)- orders of reaction
the rate constant
k, is the proportionality constant, it is the number that mathematically converts between the rate and conc of orders
overall order
=sum of orders with respect to each reactant
rate = k[A]m[B]n, m + n
shape of a zero order graph
-straight line with a negative gradient
-reaction rate does not change during the course of the reaction
gradient= k
shape of a first order graph (conc-time)
-downward curve, with a decreasing gradient over time
shape of a second order graph (conc-time)
-downward curve, but steeper at the start than 1st, and tailing off more slowly
half-life (conc-time)
- first order reactions have a constant half-life- conc halving every half-life- exponential decay
calculating rate constant from the half-life
k= ln2/ t1/2
shape of a zero order rate-conc graph
shape of a first order rate-conc graph
shape of a second order rate-conc graph
- rate= k[A]2
iodine clocks
the rate determining step
the slowest step
-rate equation only includes species involved in the rate determining step
the Arrhenius equation
k= A e-(Ea/RT)
A- pre-exponential factor
R- gas constant- 8.314 J mol-1 K-1
T-temp in K
logarithmic form of Arrhenius
In K = - Ea/RT + In A
gradient= - Ea/R