Chapter 5 AP* Chemistry

THERMOCHEMISTRY
Let’s begin with terms for you to master:
 Energy (E) – the ability to do work or produce heat ; the sum of all potential and kinetic energy in a system
is known as the internal energy of the system
 Potential energy – energy by virtue of position.
In chemistry this is usually the energy stored in
bonds (i.e., when gasoline burns there are
differences in the attractive forces between the
nuclei and the electrons in the reactants and the
products) When bonded atoms are separated, the PE
is raised because energy must be added to overcome
the coulombic attraction between each nucleus and
the shared electrons.
 When atoms bond, the above mentioned coulombic
attraction results in energy being released and a
subsequently lower PE.
 Kinetic energy – energy of motion (translational,
rotational & vibrational motion of particles in our
case), proportional to Kelvin temperature; kinetic energy depends on the mass and the velocity of the
object: KE = ½ mv2
Check out this simulation regarding the Boltzmann distribution:
http://phet.colorado.edu/en/simulation/atomic-interactions
And this one regarding the effect of temperature on molecular motion:
http://phet.colorado.edu/en/simulation/states-of-matter-basics
 Law of Conservation of Energy – You may know it as “energy is never created nor destroyed” which
implies that any change in energy of a system must be balanced by the transfer of energy either into or out
of the system.
 AKA energy of the universe is constant & the First Law of Thermodynamics
Heat (q) – Two systems with different temperatures that are in thermal contact will exchange thermal
energy, the quantity of which is call heat. This transfer of energy in a process (flows from a warmer object
to a cooler one, transfers heat because of temperature difference but, remember, temperature is not a
measure of energy—it just reflects the motion of particles)
Temperature (T)—is proportional to the average kinetic energy of the molecules, KEave .
“Heat ‘em up and speed ‘em up” as you saw in the states of matter animation.
 Enthalpy (H)– flow of energy (heat exchange) at constant pressure when two systems are in contact.
 Enthalpy of reaction (∆Hrxn) – amount of heat released (negative values) or absorbed (positive values)
by a chemical reaction at constant pressure in kJ/molrxn
 Enthalpy of combustion (∆Hcomb)—heat absorbed or released by burning (usually with O2) in
kJ/molrxn; note that combustion reactions yield oxides of that which is combusted
 Enthalpy of formation (∆Hf) – heat absorbed or released when ONE mole of compound is formed
from elements in their standard states in kJ/molrxn
 Enthalpy of fusion (∆Hfus)—heat absorbed to melt (overcome IMFs) 1 mole of solid to liquid @ MP
expressed in kJ/molrxn

Enthalpy of vaporization (∆Hvap)—heat absorbed to vaporize or boil (overcome IMFs) 1 mole liquid to
vapor @BP in kJ/molrxn
*AP is a registered trademark of the College Board, which was not involved in the production of this product. Special thanks to the contributions of
Lisa McGaw and David Wentz. © 2013 by René McCormick. All rights reserved.
 System – area of the universe we are focusing on (i.e., the experiment)
 Surroundings – everything outside of the system
 Endothermic – net absorption of energy (heat exchange) by the system; energy is a reactant; (i.e., baking
soda and vinegar when mixed get very cold to the touch) ; +ΔH
 Exothermic – net release of energy (heat exchange) by the system; energy is a product; (i.e., burning
methane gas in the lab burner produces heat; light sticks give off light which is also energy); −ΔH
 Entropy (s) – measure of the dispersal of matter and energy; increase dispersal +ΔS; decrease dispersal −ΔS
 Gibbs Free Energy (G)– criteria for determining thermodynamic favorability and calculating the
theoretical amount of energy to do work
 Thermodynamics – study of energy and its interconversions
 Work – force acting over distance in physics often expressed as work = −PΔV where gases are involved;
expressed in Joules or kJ
 Standard Conditions—you already know about STP, but recall that the T is STP is 0°C and humans are not
happy lab workers when it is that cold! So, think of standard conditions as standard lab conditions which
are 1 atm of pressure, 25°C (much more comfy!) and if solutions are involved, their concentration is 1.0 M.
All of this information is communicated by adding the symbol ° to G, H or S. So, if you see ΔH°, then you
automatically know the pressure, temperature and conditions that apply to that value!
 There has recently been a change in how enthalpy, entropy and free energy units are expressed. For
example, you may see ΔH° values expressed as kJ in older printed material. Currently, they should
be expressed in kJ/molrxn where the “molrxn” is “moles of reaction”. See Jim Spencer’s article on AP
Central for additional information.

ENERGY AND WORK

 Energy is often defined as
the “ability to do work”.
 ∆E = q (heat) + w
(work)
 Signs of q
 +q if heat absorbed
 –q if heat released
 Algebraic sign of w as it relates to work done by or work done
on gases
• + w if work done on the system (i.e., compression)
• −w if work done by the system (i.e., expansion)
 When related to gases, work is a function of
pressure
 Pressure is defined as force per unit of area, so
when the volume is changed work was either
done on the gas or by the gas.
work = −P∆V

Exercise 1 Internal Energy

Calculate ∆E for a system undergoing an endothermic process in which 15.6 kJ of heat flows and where
1.4 kJ of work is done on the system.

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Exercise 2 PV Work
Calculate the work associated with the expansion of a gas from 46 L to 64 L at a constant external pressure of
15 atm.

Exercise 3 Internal Energy, Heat, and Work

A balloon is being inflated to its full extent by heating the air inside it. In the final stages of this process, the
volume of the balloon changes from 4.00 × 106 L to 4.50 × 106 L by the addition of 1.3 × 108 J of energy as
heat. Assuming that the balloon expands against a constant pressure of 1.0 atm, calculate ∆E for the process.
(To convert between L ⋅ atm and J, use 1 L ⋅ atm = 101.3 J.)

ENTHALPY
 Measure only the change in enthalpy, ∆H ( the difference between the potential energies of the products
and the reactants)

 ∆H is a state function

 ∆H = q at constant pressure (i.e. atmospheric

pressure)

 Enthalpy can be calculated from several

sources including:
 Stoichiometry
 Calorimetry
 From tables of standard values
 Hess’s Law
 Bond energies

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  Stoichiometrically:
Exercise 4
Upon adding solid potassium hydroxide pellets to water the following reaction takes place:
KOH(s) → KOH(aq) + 43 kJ/mol

Answer the following questions regarding the addition of 14.0 g of KOH to water:
Does the beaker get warmer or colder?
Is the reaction endothermic or exothermic?
What is the enthalpy change for the dissolution of the 14.0 grams of KOH?

 Calorimetry:

The process of measuring heat based on observing the temperature change when a body absorbs
or discharges energy as heat.

“Coffee Cup” calorimetry:

Coffee-cup calorimetry – in the lab this is how we experiment to find energy of a

particular system. We use a Styrofoam® cup, reactants that begin at the same temperature
and look for change in temperature. After all data is collected (mass or volume; initial
and final temperatures) we can use the specific formula to find the energy released or
absorbed. We refer to this process as constant pressure calorimetry. ** q = ∆H @ these
conditions**

Terms to know:

 Heat capacity – energy required to raise temp. by 1 degree (Joules/ °C)

 Specific heat capacity (Cp) – same as above but specific to 1 gram of substance and the experiment is
carried out at constant pressure. Constant pressure is achieved using open containers, so you will be doing
experiments of that kind in lab.

quantity of heat transferred

specific heat =
( g of material) (degrees of temperature change)

Molar heat capacity—same as above but specific to one mole of substance (J/mol K or J/mol °C )

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 Energy (q) released or gained at constant pressure: q = mCp∆T
q = quantity of heat (Joules or calories)
m = mass in grams
ΔT = Tf −Ti (final – initial)
Cp = specific heat capacity ( J/g°C)

 Specific heat of water (liquid state) = 4.184 J/g°C ( or 1.00 cal/g°C)

Water has one of the highest specific heats known! This property makes life on earth possible and regulates
earth’s temperature year round!

 Heat lost by substance = heat gained by water

 Units of Energy:
 calorie--amount of heat needed to raise the temp. of 1.00 gram of water 1.00 °C
 kilocalorie—1,000 calories AND the food label calorie with a capital C.
1 kg×m
KE = mv 2 units are
2 s2
 joule--SI unit of energy; 1 cal = 4.184 J

Exercise 5
In a coffee cup calorimeter, 100.0 mL of 1.0 M NaOH and 100.0 mL of 1.0 M HCl are mixed. Both
solutions were originally at 24.6°C. After the reaction, the final temperature is 31.3°C. Assuming that all
solutions have a density of 1.0 g/cm3 and a specific heat capacity of 4.184 J/g°C, calculate the enthalpy
change for the neutralization of HCl by NaOH. Assume that no heat is lost to the surroundings or the
calorimeter.

Exercise 6 Enthalpy
When 1 mole of methane (CH4) is burned at constant pressure, 890 kJ/mol of energy is released as heat.
Calculate ∆H for a process in which a 5.8 gram sample of methane is burned at constant pressure.

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Exercise 7 Constant-Pressure Calorimetry

When 1.00 L of 1.00 M Ba(NO3)2 solution at 25.0°C is mixed with 1.00 L of 1.00 M Na2SO4 solution at 25°C
in a calorimeter, the white solid BaSO4 forms and the temperature of the mixture increases to 28.1°C.
Assuming that the calorimeter absorbs only a negligible quantity of heat, and that the specific heat capacity of
the solution is 4.18 J/°C ⋅ g, and that the density of the final solution is 1.0 g/mL, calculate the enthalpy change
per mole of BaSO4 formed.

 Tables:
♦ ∆Hf° = enthalpy of formation

= Production of ONE mole of compound FROM

its ELEMENTS in their standard states (°)

= ZERO (0.00) for ELEMENTS in standard states

♦ Standard States: 25°C (298 K), 1 atm, 1M

The “Big Mamma” Equation: ∆Hrxn = Σ ∆Hf (products) - Σ ∆Hf (reactants)

(also known as Hess’s Law)

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Exercise 8
Substance ∆Hf° (kJ/mol)
NH4ClO4(s) −295
Al2O3(s) −1676
AlCl3(s) −704
NO(g) 90.0
H2O(g) −242

Given the information above, calculate the ∆H°rxn for the following chemical reaction.

3 Al(s) + 3 NH4ClO4(s) → Al2O3(s) + AlCl3(s) + 3 NO(g) + 6 H2O(g)

Exercise 9 C6H12O6(s) + 6 O2(g) → 6 CO2(g) + 6 H2O() + 2800 kJ

Occasionally, not all values are found in the table of thermodynamic data. For most substances it is impossible
to go into a lab and directly synthesize a compound from its free elements. The heat of formation for the
substance must be calculated by working backwards from its heat of combustion. Calculate the ∆Hf of
C6H12O6(s) given the combustion reaction above along with the following information.

Substance ∆Hf° (kJ/mol)

CO2(g) −393.5
H2O() −285.8

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Exercise 10
The thermite reaction occurs when a mixture of powdered aluminum and
iron(III) oxide is ignited with a magnesium fuse. Using enthalpies of formation,
calculate the standard change in enthalpy for the thermite reaction:

2Al (s) + Fe2O3(s) → A12O3(s) + 2Fe(s)

Enthalpy is independent of the reaction pathway. If you can find a combination of chemical equations that add
up to give you the desired overall equation, you can also sum up the ∆H’s for the individual reactions to get the
overall ∆Hrxn.

♦ First, decide how to rearrange equations such that the reactants and products are on appropriate sides of the
arrows in the chemical equation. It is often helpful to begin by working backwards from the final or
summary chemical equation.
♦ If an equation had to be reversed, also reverse the sign of ∆Hrxn
♦ If an equation had to be multiplied by a given factor to obtain correct coefficients, also multiply the
∆H rxn by this factor since ∆Hrxn’s are in kJ/MOLErxn (division applies similarly)
♦ Double check to ensure that everything cancels out to give you the exact summary chemical equation you
desire.

Exercise 11
Calculate the ∆H for this overall reaction 2 H3BO3(aq) → B2O3(s) + 3 H2O() given the following
equations:
H3BO3(aq) → HBO2(aq) + H2O() ∆H = −0.02 kJ/molrxn
H2B4O7(aq) + H2O() → 4 HBO2(aq) ∆ H = −11.3 kJ/molrxn
H2B4O7(aq) → 2 B2O3(s) + H2O() ∆ H = 17.5 kJ/molrxn

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 Bond Energies
• Energy must be added/absorbed to BREAK bonds (endothermic) in order to overcome the
coulombic attraction between each nuclei and the shared electrons. Energy is released when
bonds are FORMED (exothermic) because the resultant coulombic attraction between the
bonded atoms lowers potential energy causing a release. This is a giant misconception among
students! Once again, it “takes” energy to break bonds and energy is released when a bond
forms.

• ∆H = sum (Σ) of the energies required to break old bonds (positive signs since energy is added to
the system) plus the sum of the energies released in the formation of new bonds (negative signs
since energy is lost from the system).

∆H = Σ Bond Energies broken – Σ Bond Energies formed

Exercise 12
Calculate the change in energy that accompanies the following reaction given the data below.

H2(g) + F2(g) → 2 HF(g)

Bond Type Bond Energy

H−H 432 kJ/mol
F−F 154 kJ/mol
H−F 565 kJ/mol

 SUMMARY FOR ENTHALPY: What does it really tell you about the changes in energy regarding a
chemical reaction?
 ∆H = + reaction is endothermic and heat energy is added into the system
 ∆H = − reaction is exothermic and heat energy is lost from the system
(Nature tends toward the lowest energy state!)

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Speaking of bond energies, allow us to clear up some common misconceptions AND make
some dazzling connections.
Let’s start with the vocabulary used to describe phase changes. First, you must realize that the vocabulary is
“directional” (hence the arrows on this diagram) as well as very specific. You’ll have to mean what you say
and say what you mean when answering a free response question!

Phase transitions involving overcoming intermolecular attractions or IMFs

which should never be confused with ionic or covalent chemical bonds.

Fusion (melting), vaporization, and sublimation require an input of

energy to overcome the attractive forces between the particles of the
substance. NOTICE we did not speak of “breaking bonds”.

Freezing, condensation, and deposition (opposite of sublimation) release

energy as IMFs form since the particles achieve a lower energy state
mainly due to a decrease in temperature.

Is there a difference between a vapor and a gas? Yes, it’s primarily semantics. A gas is a gas at
room temperature, we don’t speak of “oxygen vapor”. However, we do use the term “vapor” when
the substance is normally a liquid or solid at room temperature. We say “water vapor”, “carbon
dioxide vapor”, “iodine vapor”, etc.

Be very, very clear that changes in the phases of matter involve altering IMFs, not altering
chemical bonds.*

The strength of the intermolecular attractions between molecules, and therefore the amount of
energy required to overcome these attractive forces (as well as the amount of energy released when
the attractions are formed) depends on the molecular properties of the substance, ionic, polar,
nonpolar, etc.

Generally, the more polar a molecule is, the stronger the attractive forces between molecules
are. Hence, more polar molecules typically require more energy to overcome the intermolecular
attractions in an endothermic phase transition, and release more energy by forming intermolecular
attractions during an exothermic phase transition.

Phase transitions involve the “breaking” or forming of intermolecular forces (attractive interactions
between molecules). Hence, as with other chemical reactions, it is necessary to discuss the energy
that is absorbed or given off during the breaking or forming of intermolecular interactions in a
phase transition.
*UNLESS you have a network solid or covalent network solid which is a chemical compound in which the atoms are bonded by
covalent bonds in a continuous network. In a network solid there are no individual molecules and the entire crystal may be considered
a macromolecule. Examples of network solids include diamond with a continuous network of carbon atoms and silicon dioxide or
quartz with a continuous three dimensional network of SiO2 units. Graphite and the mica group of silicate minerals structurally consist
of continuous two-dimensional layers covalently bonded within the layer with other bond types holding the layers together. That
means they essentially slide in sheets the way your pencil “lead” (actually graphite) glides across the page leaving a trail.

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You have probably seen a graph like this before arriving in AP Chemistry. Let’s make some additional
dazzling connections!
Suppose this heating curve is for water (it isn’t because the horizontal line for boiling  condensing is too
short. Why? (It takes WAY more energy to boil water than what is shown here due to having to overcome all
those IMFs called hydrogen bonds).

Take a moment and ponder the differences in molecular structure and molecular motion among the different states of
water represented above, the kinetic energy changes, and the potential energy changes.

1. Does the process above represent a collection of chemical changes, physical changes or both?

2. What type of force is involved in the changes you identified in question 1?

3. Define temperature:

4. Which conversions involve temperature changes?

5. Which mathematical formula is appropriate for calculating the energy associated with the processes you
identified in question 4?

6. Which conversions involve potential energy changes?

7. Which mathematical formula is appropriate for calculating the energy associated with the processes you
identified in question 4?

8. How do you calculate q for the processes identified in number 6 if you are given only the mass of the water
sample?

9. Which portions of this graph represent equilibrium conditions?

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