enthalpy changes: content Flashcards
(23 cards)
exothermic reactions
the products are at a lower energy than the reactants: excess heat is transferred from the system to the surroundings
ΔH is negative
endothermic reactions
products are at a higher energy than the reactants: heat is taken in from the surroundings to the system
ΔH is positive
enthalpy profile diagrams
- gaseous atoms
- reactants
- products
standard conditions [ ]ᶿ
298K
100kPa
1.00moldm⁻³
standard enthalpy change of formation for an element
zero (by definition)
examples of exothermic reactions
combustion
respiration
neutralisation
examples of endothermic reactions
thermal decomposition
evaporation
photosynthesis
what are the two calorimetry equations
q=mcΔT
q - energy change (J)
m - mass of solution/surroundings (g)
c - specific heat capacity of solution/surroundings (J kg⁻¹ K⁻¹)
ΔT - temperature of solution/surroundings (K)
ΔH=±q/n
ΔH - enthalpy change (kJ mol⁻¹)
q - enthalpy change (kJ)
n - moles of reactant/system (mol)
methods to determine enthalpy changes
combustion calorimetry
calorimetry with a reaction in solution
combustion calorimetry overview
a known mass of substance/fuel is burned to heat a known mass of water
system- fuel burning
surroundings- water
ALWAYS exothermic - ΔH is negative
sources of error in combustion calorimetry
- heat lost to the air
- incomplete fuel combustion
[evaporation of fuel/water from wick/beaker]
how to minimise error in combustion calorimetry
- ensure a plentiful oxygen supply (in excess)
- add a lid to the beaker
- use a copper can instead of a beaker (better conductor)
- cover wick when not burning
- use an insulated/bomb calorimeter
calorimetry with a reaction in solution overview
a known quality of reactant (limiting!!) reacts in a known volume of water
system- the chemicals reacting or dissolving
surroundings- the solution
sources of error in reaction in solution calorimetry
- heat loss/gain to/from the air
- water evaporates from the beaker
- incomplete reaction
- c of solution ≠ c of water
how to minimise error in reaction in solution calorimetry
- use a polystyreine cup
- use a lid to prevent heat loss/gain
- ensure standard conditions
bond enthalpies are always _____
endothermic (positive ΔH values)
bond breaking is
endothermic
(=activation energy)
bond making is
exothermic
how to calculate ΔH
- draw out the equation
- calculate totals for bonds made/broken
- use the equation to calculate overall enthalpy changes
- [sketch reaction profile]
why can reactions be exothermic
more energy is released (forming bonds in the products) than is required (breaking bonds in the reactants)
why might it not be possible to directly measure enthalpy changes from experiments
- very high activation energy Eₐ
- very slow rate of reaction
- occurrence of side reactions
how to indirectly calculate enthalpy changes
hess’ law: the enthalpy change for a given reaction is independant of the route taken
draw an enthalpy cycle (kinda like vectors)
BE CAREFUL of the enthalpy change direction
required practical: enthalpy determination
- pour the aqueous reactant into a polystyreine cup and cover
- use a thermometer to record the temperature every minute for three minutes to get an accurate start temperature
- add the other reactant and stir to ensure a homogenous mixture
- record the temperature after one minute
- continue to record the temperature at one minute intervals
- calculate ΔT
- plot ΔT against time
- extrapolate two lines of best fit
- read ΔT at the point of mixing