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kinetic energy
energy in motion
thermal energy
energy associated with the random motion of atoms and molecules
potential energy
energy possessed by an object by virtue of its position
chemical energy
energy stored within the structural units of chemical substances
stored inside the bonds
electrostatic energy
potential energy that results from the interaction of charged particles
electrons coming loose (ex. rubbing a balloon on your hair)
Law of conservation of energy
energy can neither be created nor destroyed
when energy of one form disappears, the same amount of energy reappears in another form/forms
System
a part of the universe that is of specific interest
UNIVERSE = SYSTEM + SURROUNDINGS
Surroundings
constitute for the rest of the universe outside the system
UNIVERSE = SYSTEM + SURROUNDINGS
thermochemistry
study of heat in chemical reactions
Heat
transfer of thermal energy
exothermic process
when heat is transferred from the system to the surroundings
feels hot because heat is being gained and we are in the surroundings
heat added within the product
endothermic process
when heat is transferred from the surroundings to the system.
feels cold because heat is being lost and we are in the surroundings
heat is added within the reactants
State Functions
properties that are determined by the state of the system
energy = state function
magnitude of change depends only one the initial and final states of the system
volume
pressure
temperature
energy
First law of therodynamics
energy can be converted from one from to another but can not be created nor destoryed
delta U of system = - delta U of surroundings
delta U of system + delta U of surroundings = 0
energy goes up = exothermic reaction
energy goes down = endothermic reaction
thermodynamics
study of the conversion of heat and other kinds of energy
three different systems
Open system
can exchange energy and mass with the surroundings
Closed system
allows transfer of hear to surroundings but not mass
Isolated System
doesn’t exchange mass nor energy with the surroundings
IDEAL SYSTEM
work and heat: Δu = q+w
the overall charge in the systems internal energy and is given by: Δu=q+w
q = heat
q is positive for endothermic processes - GAINING HEAT
q is negative for exothermic processes - LOOSING HEAT
w = work
w is positive for work done ON the system - VOLUME DECREASES
w is negative for work done BY the system - VOLUME INCREASES
Volume of the system
under constant volume conditions, pressure increases
the volume of a system can change- if the volume can’t change the pressure changes
LESS VOLUME = MORE PRESSURE
Enthalpy (H)
thermodynamic function of a system
H= U+PV
change in enthalpy / change in heat of system (ΔH)
what we are interested in when a thermochemical reaction occurs. It is equal to the heat exchanged between the system and the surroundings for a constant pressure system.
change in this = change in internal temperature
ΔH = ΔU + Δ(PV)
constant pressure process- qp=ΔH
qp= ΔU +PΔV
enthalpy of reaction ΔH
the difference between the enthalpies of the products and the enthalpies of the reactants
ΔH = H(products) - H(reactants)
ΔH > 0 (positive) = endothermic process, heat lost
ΔH < 0 (negative) = exothermic process, heat gained
ex. H2O(s) → H2O(l), ΔH = +6.01 kJ/mol
heat is absorbed by the system from the surroundings- H2O(s) + 6.01 : kJ/mol → H2O (J)
ΔH>0 = endothermic process
enthalpy is an extensive property, this means…
it depends on how much there is. It is dependent on the amount of matter involved.
Guidelines for thermochemical equations
always specify the physical states of reactants and products because they help determine the actual enthalpy charges
when multiplying an equation by a factor (n), multiply the ΔH value by the same factor
double the whole equation
reversing the equation changes the sign but not the magnitude of ΔH
if the ΔH is positive, it becomes negative
if the ΔH is negative, it becomes positive
calorimetry
the measurement of heat changes are measured on a device called a caloimeter
s = J / S °C
Specific Heat (s)
the amount of eat required the raise the temperature of one gram of of the substance by one degree Celcius
Heat Capacity (C)
the amount of heat required to raise the temperature of an object by one degree celcius
the “object” may be given quantity of a particular substance
specific heat capacity units: J/(g*°C)
heat capacity unit: J/°C
q=smΔt
how the heat associated with a temperature change is calculated
m=mass, s= specific heat, ΔT= change in temperature
ΔT= (Tfinal - Tinital)
Transfer of Heat
qp=ΔH
q(sys) = -msΔT, q(surr) = msΔT
q(sys) = -q(surr)
(msΔT)sys = -(msΔT)surr
the minus sign is used the keep sign conversions consistant
Constant-Volume Bomb
how constant volume calorimetry is carried out
constant volume calorimeter is an isolated system
bomb calorimeters are used to determine heats of combustion- q(cal) = -q(rxn)
calculating q(cal)
the heat capacity of the calorimeter must be known
q(cal) =CcalΔT
q(rxn) = -q(cal)
q(rxn) = -CcalΔT
Hess’s Law
the change in enthalpy for a stepwise process is the sim of the enthalpy changes for each of the steps
Steps for applying Hess’s Law
manipulate thermochemical equations in a manner that gives the overall desired equation
remember the rules for manipulating thermochemical equations
add the ΔT for each step after proper manipulation
process is useful for calculating enthalpies that cannot be found directly
Standard enthalpy of formation (ΔH°f)
the heat change that results when one mole of a compound is formed from its constituent elements in their standard states
ΔH°rxn = ∑nΔH°f(products) - ∑mΔH°f(reactants)
change in ΔH = sum of products - sum of reactants
Bond Enthalpy
the enthalpy change associated with breaking a bond in one mole of gaseous molecule
ΔH°= ∑BE(reactants) - ∑BE(products)
total energy output (bonds broken) - total energy released (bonds formed)
breaking takes energy = POSITIVE
making gives off energy = NEGATIVE