A chemical reaction that absorbs energy from the surroundings (ΔH = +ve)
Endothermic reactions
H2O(s) → H2O(l) ΔH = 6kJ
C2H5OH(l) + 43kJ → C2H5OH(g)
Enthalpy change (ΔH)
Theenergyexchange between a chemical reaction and its surroundings at constant pressure
Enthalpy change (ΔH) = enthalpy of products - enthalpy of reactants
Rate of reaction
The speed at which reactants are used up or products are formed
Graph of rate of reaction
Steepest slope at start when concentrations are maximum
Curve steadily gets less steep as reactants are used up
Curve levels off at end when all reactants have been used
Collision theory
Reacting particles must collide in the correct orientation and with sufficient energy to overcome the activation energy barrier
Successful collision
Correct orientation and sufficient energy to result in a reaction
Activation energy (Ea)
The minimum amount of energy molecules must have in order for the reaction to take place
According to collision theory, a reaction will speed up if the frequency of collisions increases or the proportion of particles with energy greater than the activation energy increases
Effect of concentration on rate of reaction
More concentrated reactants have a faster rate of reaction due to more frequent collisions
Effect of pressure on rate of reaction
Increasing pressure of reacting gases increases the number of gas molecules in a given volume, leading to more collisions and a faster rate of reaction
Effect of state of subdivision on rate of reaction
Smaller size particles provide a larger surface area, increasing the chances of collisions and the rate of reaction
Maxwell-Boltzmann distribution
At a given temperature, particles will not all possess the same amount of energy
Increasing temperature shifts the curve to the right and flattens it, increasing the proportion of particles with energy greater than the activation energy
A 10°C rise in temperature approximately doubles the rate of a reaction
Catalyst
A substance that speeds up a chemical reaction by providing an alternative pathway with lower activation energy, without being consumed in the process
Effect of catalyst on activation energy
Catalyst lowers the activation energy, increasing the proportion of particles with sufficient energy to react
Catalyst does not affect the shape of the Maxwell-Boltzmann distribution
Rate determining step
The slowest step in a multi-step reaction, which governs the overall rate
The rate equation may not contain all the reactants if there is more than one step
Most chemical reactions are considered irreversible - the products cannot readily be changed back into the original reactants
Reversible reaction
A reaction that can go in either direction, where the products can react together to reform the original reactants
Reversible reactions have low activation energies for both the forward and reverse reactions, and do not go to completion
Characteristics of equilibrium
Requires a closed system
Is dynamic - forward and reverse reactions occur at the same rate
Concentrations of reactants and products remain constant
In homogeneous equilibria, all reactants and products are in the same phase. In heterogeneous equilibria, reactants and products are present in more than one physical state
For heterogeneous equilibria, the concentrations of pure solids and liquids are omitted from the equilibrium constant expression
Interpreting the equilibrium constant
If K > 1 x 10^4, products are favored over reactants
If K < 1 x 10^-4, reactants are favored over products
Types of equilibria
Homogeneous
Heterogeneous
Homogeneous equilibria
Include all (g), (l), (s), (aq)
Heterogeneous equilibria
Omit (s) and (l), include (g) and (aq)
Solids and liquids are NOT included in the K expression of heterogeneous reactions. The concentration of a solid does not vary, nor does the concentration of liquid (water) in an aqueous solution.
Interpreting the equilibrium constant
If K > 1 x 10^4, products are favored over reactants
If K < 1 x 10^-4, reactants are favored over products
The value of K varies only with temperature
For endothermic reaction
K increases with increasing temperature
For exothermic reaction
K decreases with increasing temperature
Factors that do not change K: concentration/partial pressure, total pressure, catalyst