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Endothermic enthalpy profile diagram
Exothermic enthalpy profile diagram
Enthalpy change
The heat energy transferred during a reaction at constant temperature
What happens in an exothermic reaction?
Energy is transferred from the system to the surroundings
What happens in an endothermic reaction
Energy is transferred from the surroundings to the system
How can you tell an energy profile represents an exothermic reaction
The products are at a lower energy than the reactants
Examples of exothermic reactions
Combustion
Respiration
Neutralisation - H=-57kJmol-
How can you tell an energy profile represents an endothermic reaction?
The products are at a higher energy than the reactants
Examples of endothermic reactions
Photosynthesis
Thermal decomposition
Melting of ice
Activation energy
The minimum energy required for a reaction to take place
Standard conditions
Temperature - 298K
Pressure - 100kPa
All solutions at - 1 moldm-3
Standard enthalpy change of a reaction
The enthalpy change for a given reaction in the molar quantities shown in the equation
Can be either a endothermic or exothermic reaction
Standard enthalpy of combustion
The enthalpy change when 1 mol of a substance completely combusts at 298K and 100kPa
Exothermic reaction
Standard enthalpy of formation
The enthalpy change when 1 mol of a compound is formed from its elements at 298K and 100kPa
Can be either endothermic or exothermic
Enthalpy of formation of an element is zero by definition
Standard enthalpy change of neutralisation
The enthalpy change when 1 mol of H2O is formed from a reaction of H+ and OH-
Always an exothermic reaction
Calorimetry
q=mcΔt
q = energy change - J
m = mass of solution - g
c = specific heat capacity - Jg-1K-1
Δt = Change in temperature of solution .C or K
Calorimetry 2
ΔH = +-q/n
ΔH = enthalpy change - kJmol-1
q = energy change - kJ
n = moles of reactant
If there are 2 reactants we would use the limiting reactant
Combustion Calorimetry
The water acts as the surroundings
The fuel burning acts as the chemical system
How come the calculated value from an experiment is different to the data book in combustion calorimetry?
Heat loss to surroundings
Incomplete combustion will occur
How to reduce sources of error in combustion calorimetry
Ensure a ventilated room
Move beaker closer to the flame
Copper beaker instead of glass beaker
Add a lid to the beaker
Cover the wick
Calorimetry with a reaction in solution
The solution acts as the surroundings
The chemical reacting or dissolving acts as the chemical system
Sources of error in calorimetry reaction in solution
Heat loss/gain to/from surroundings
Water evaporates from the beaker
Incomplete reaction
C of solution is not the same as water
How to minimise these errors
Use a polystyrene cup
Use a lid to prevent heat loss/gain
Ensure standard conditions
Predicting temperature changes 1
ΔH is the same, If n is doubled q is doubled, Volume is doubled, So Δt is doubled
Predicting temperature changes 2
ΔH is the same, If n is halved q is halved, volume is halved, Δt stays the same
Average bond enthalpy
The enthalpy change for the breaking of 1 mole of bonds in gaseous molecules
Bond enthalpies
The bond enthalpy value indicates the strength of a covalent bond
The more positive the bond the larger the amount of energy needed to break the bond so the stronger the bond
Why is a reaction exothermic?
The energy required to break the bond is less than the energy released when making bonds
Why is a reaction endothermic?
The energy required to break the bonds is more than the energy released when making the bonds
Mexican Ben
ΔrH
ΣΔBeH (bonds broken) - ΣΔBeH (bonds formed)
Why is it not always possible to measure enthalpy changes directly from experiments?
A very high activation energy
A very slow rate of reaction
Occurrence of side reactions
Enthalpy of Combustion Hess’s Law
Enthalpy of Formation Hess’s Law