Thermochemistry
Thermochemistry
Definition: The study of energy changes associated with chemical reactions or physical transformations
Ex: phase changes, dissolving
focuses on a system’s exchange of energy within its surroundings (releasing energy into surroundings> surroundings absorb reaction’s energy)
Endothermic Process - a system that absorbs energy from its surroundings (heat is on the reaction side, 🔼H is positive) (low to high)
Exothermic Process - a system that releases energy to its surroundings (heat is on the product side, 🔼H is negative) (high to low)
Heat - energy that’s transferred due to a difference in temperature
always occurs from warmer (high kinetic energy) to cooler (low kinetic energy)
results in both objects reaching the same temperature, known as thermal equilibrium
Thermochemical equations - any equation with heat in it
Enthalpy (H)
a form of chemical energy (potential energy)
referred to as “heat contact.”
can’t be measured directly —> but can measure how it changes during a reaction
🔼H = Hf - Hi (final - initial)
Heat Capacity & Substance
Definition: a measure of how well the substance stores/transfers energy
Heat Capacity (uppercase C) - amount of heat absorbed or released / change in temperature
Specific heat capacity (“specific heat”) (lowercase c) - amount of heat required to raise the temperature of 1 gram of a pure substance by 1 °C (or 1 Kelvin)
specific heat of water: 1 cal/g•°C or 4.184 J/g•°C
q = mc🔼T (c is always unique to the substance)
1 mL = 1 gram
Bomb Calorimeter
Definition: often used to measure 🔼H of combustion reactions (🔼Hc)
The reaction chamber is surrounded by an H2O “jacket” and then an insulation layer with steel boxes separating each layer, a thermometer, and stir sitting in the H2O jacket
-q(reaction) = +q(calorimeter) —> exothermic, calorimeter absorbs the heat released by the reaction —> temperature goes up in calorimeter
+q(reaction) = -q(calorimeter) —> endothermic, calorimeter releases heat absorbed by the reaction —> temperature goes down in calorimeter
The calorimeter is constructed with different substances, each with a different specific heat capacity
q(whole calorimeter) = mc🔼T (steel) + mc🔼T(H2O) + mc🔼T(insulation) + …
q(cal) = 🔼T(mc(steel) + mc(H2O) + mc(insulation))
q(cal) = C🔼T (C —> uppercase, heat capacity of whole calorimeter, units: J/°C or kJ/°C)
multiple trials are run with the same calorimeter to determine “C” (heat capacity)
Phase Change
endothermic (adding heat, KE) —————————————>
melting (fusion) boiling (vaporization)
solid ————-————→ liquid ——-———————-→ gas
solid ←——————--—-- liquid <——————————-gas
freezing (solidification) condensation
sublimation
solid ————————————————————-——>gas
solid <—————--——————————————-——-gas
deposition
←————————————-exothermic (taking out heat, KE)
H(f) = heat of fusion
amount of energy required to melt 1 gram of a solid at its melting point
H(v) = heat of vaporization
amount of energy required to vaporize 1 gram of liquid at its boiling point
KE is when temperature is being raised, heat is added, energy increases
PE is when there is no change in temperature'
On the heating graph, you need melting point (solid —> liquid) and a boiling point (liquid —> gas)
Equations:
q = mc🔼T (whenever temp changes, c depends on whether it is solid/gas or liquid)
q = mH(f) (no temp change)
q = mc🔼T
q = mH(v) (no temp change)
q = mc🔼T