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rate of reaction
how quickly reactants are used or products are formed
fast = high #
RoR equation
amount of reactant used / amount of product formed (unit g)
divided by
time taken
collision theory
particles must collide with enough energy & in the correct orientation to react successfully
change in temperature
increase: reactant particles move faster, more KE than Ea
collide more often with more force = greater freq of success
RoR increase
change in pressure
volume decreases(particles the same)
crowded particles likely to collide more often
greater freq. of successful collisions
RoR increase
changing solution conc
more reactant particles in a fixed volume
crowded particles likely to collide more often
greater freq. of successful collisions
RoR increase
adding a catalyst
RoR increases, yield remains unchanged
nothing changes about the catalyst post-reaction
solid catalysts need a larger surface area to catalyze faster
changing surface area in reaction
smaller pieces of the same mass will have a larger surface area
more particles at surface = more exposed to react
RoR gas product measuring equipment
collecting gas formed in gas syringe over time
calculated mean rate up until a given time
calculate rough gradient with RATs
(sometimes the phrase after is used. representing how much time has passed)
mean RoR between times
Calculate change in volume & time. (change y-axis = vol // change x-axis= time)
Insert change into gradient equation
mean RoR AT a specific time
draw tangent line, balanced on either side when the tangent stops touching the curve
reversible reactions
chemical reaction that can proceed in either direction
products can also react to form the reactants
dynamic equilibrium
rate of forward reaction (equal to rate of reverse reaction)
mass of reactants/products don’t have to be equal but do not change
dynamic equilibrium (3 marks)
conc of reactants & products do not change
ONLY occurs with reversible reactions in closed system
rate of forward = rate of reverse
equilibrium position
gives an idea of comparative amounts of reactants to products
if lying to the left = reactant conc > product conc
equilibrium position temp
decrease in temp shifts eqp in exothermic direction, vice versa for endothermic
a negative kJ/mol is exothermic
this occurs to counteract the change
equilibrium position conc
if conc of substance is increased, eqp moves in direction away from substance & vice versa
equilibrium position pressure
increasing the pressure of a system with gases present will shift the equilibrium to the side with fewer molecules of gas
haber process equation
N2 + 3H2 ⇌ 2NH3
why is an iron catalyst used?
lowers Ea, so lower temp can be used while RoR increases
cost-effective
why is 450c used in the haber process?
low temp needed to favor forward reaction
high temp needed to increase Ke for collisions
why is 200 atm used?
high pressure » equilibrium to the right from increased collisions
may have high costs and safety concern so 200 is a compromise