Chapter 7: Kinetic Theory, Thermochemistry, Calorimetry, & Hess's Law
1 Calorie (Cal) or kilocalorie (kcal) =
1000 cal = 4184 J
1 Kilowatt-hour (Kwh) =
3.60 * 10^6 J
ΔE =
Efinal - Einitial
Effusion
The movement of gas molecules through a tiny hole into a vacuum
q
heat (thermal) energy
Heat exchange
heat is exchanged of thermal energy between a system and surroundings
q =
m*cs*∆T
Define heat
the flow of energy caused by a temperature difference
System
the material or process within which we are studying the energy changes within
∆Hrxn =
Σn∆Hf (products) - Σn∆Hf (reactants)
C(s) + O2(g) > CO2(g) ∆H = -393.5 kJ 2 C(s) + 2 O2(g) > 2 CO2 (g) CO2(g) > C(s) + O2(g)
∆H = 2(-393.5 kJ) = -787.0 kJ ∆H = +393.5 kJ
Using the following equation for the combustion of octant, calculate the heat associated with the combustion of 150.0 g of octant assuming complete combustion. The molar mass of octant is 114.33 g/mole/ the molar mass of oxygen is 31.9988 g/mole 2 C8H18 + 25 O2 > 16 CO2 + 18 H2O ∆Hrxn = -11018 kJ
∆Hrxn = -7228 kJ
Use the standard reaction enthalpies given below to determine ΔH°rxn for the following reaction: 4 NO(g) + 2 O2(g) > 4 NO2(g) ΔH°rxn = ? Given: N2(g) + )2(g) > 2 NO(g) ΔH°rxn= +183 kJ 1/2 Ns(g) + O2(g) > NO2(g) ΔH°rxn= +33 kJ
-234 kJ
Two solutions, initially at 24.69 °, are mixed in a coffee cup calorimeter. When a 200.0 mL volume of 0.100 M AgNO3 solution is mixed with a 100.0 mL samples of 0.100 M NaCl solution, the temperature in the calorimeter rises to 25.16°. Determine the ΔH°rxn, in units of kJ/mol AgCl/ Assume that the density and heat capacity of the solution is the same as that of water. Hint: Write a balanced reaction for the process. The specific heat capacity of water = 4.18 J/g°C.
-59 kJ/mol AgCl
Which of the following (with specific heat capacity provided) would show the largest temperature change upon gaining 200 J of heat? 50.0 g Al, CAl = 0.903 J/g°C 50.0 g Zn, CZn = 0.39 J/g°C 25.0 g Ag, CAg = 0.235 J/g°C 25.0 g Hg, CHg = 0.14 J/g°C 25.0 g granite, Cgranite = 0.79 J/g°C
25.0 g Hg, CHg = 0.14 J/g°C
Use the standard reaction enthalpies given below to determine ΔH°rxn for the following reaction: 8 SO3(g) > 8 S(s) + 12 O2(g) ΔH°rxn= ? Given: SO2(g) > S(s) + O2(g) ΔH°rx= +296.8 kJ 2 SO2(g) + O2(g) > 2 SO3(g) ΔH°rxn= -197.8 kJ
3166 kJ
1 calorie (cal) =
4.184 joules (J)
What volume of benzene (C6H6, d= 0.88 g/mL, molar mass = 78.11 g/mol) is required to produce 1.5 × 103 kJ of heat according to the following reaction? 2 C6H6(l) + 15 O2(g) → 12 CO2(g) + 6 H2O(g) ΔH°rxn = -6278 kJ
42 mL
Bomb Calorimeter
Has a constant volume & is used to measure ∆E for combustion reactions
Thomas Graham
discovered that the effusion rate of a gas is inversely proportional to the square root of its density (d)
Exchange of work
w = -pressure * ∆Volume
Thermal equilibrium
when two objects are at the same temperature and no heat flows
w
work energy
Conservation of energy requires that the total energy change in the system & the surrounding must be zero
ΔEnergyUniverse = 0 = ΔEnergySystem + ΔEnerguSurroundings
Insulated cup with 75.0 g of H2O @ 24.00 °C 26.00 g sample of metal @ 82.25°C Final temperature of water & metal = 28.34°C What is the specific heat of the metal?
*No loss of heat, heat is directly transferred from water to metal of vice versa. (insulated cup) 82.25-28.34=53.91°C 28.34-24.00=4.34°C qH2O = 75g*4.184J/g°C*4.34°C qH2O = 1360.59 J 1360.59 J = 26.00 g * Cs * 53.91 °C Csmetal = 1360.59/26.00g*53.91°C Csmetal = 0.9706 J/g°C
When energy flows into the surroundings, ΔEsurroundings is
+
When energy flows out of a system, ΔEsystem is
-
First law or thermodynamics
- Energy can neither be created not destroyed, but can be transferred from one type of energy to another - The total energy of the universe is constant - Example: chemical energy > thermal energy
When a system absorbs energy...
- The system is said to be "endothermic" - The system becomes warmer, & the surroundings become colder
When a system releases energy...
- The system is said to be "exothermic" - The system becomes colder & the surroundings become warmer
q & w
- are not state functions - ΔE = q + w
Kinetic energy
- energy of motion - energy being transferred
Heat capacity, cs
- quantity of heat energy absorbed - J/degrees celsius
In practice, we can't observe temp. change of the individual chemicals involved in a reaction, so instead we measure the temp. change in the surroundings
- use insulated, controlled surroundings - +qsys = -qsurr.
Use the following equation for the combustion of octane, calculate the heat associated with the combustion of excess octant with 100.0 g oxygen assuming complete combustion. The molar mass of octane is 114.33 g/mole. The molar mass of oxygen is 31.9988 g/mole. 2 C8H18 + 25 O2 > 16 CO2 + 18 H2O ∆Hrxn = -11018 kJ
-1377 kJ
Use the standard reaction enthalpies given below to determine ΔH°rxn for the following reaction: 4 S(s) + 6 O2(g) > 4 SO3(g) ΔH°rxn= ? Given: SO2(g) > S(s) + O2(g) ΔH°rx= +296.8 kJ 2 SO2(g) + O2(g) > 2 SO3(g) ΔH°rxn= -197.8 kJ
-1583 kJ
335 g H2O 24.5 degrees celsius - 26.4 degree celsius Cs for H2O = 4.184 J/g °C
1.) Calculate heat, q q = m*cs*∆T q = 335g *4.18 J/g°C*1.9°C q = 2660.57 J 2.) Is the heat absorbed or released ABSORBED
Forms of potential energy
1.) Chemical 2.) Elastic 3.) Nuclear 4.) Gravitational
Kinetic theory of gases
1.) Gas particles are tiny & in constant, random motion 2.) Gas particles occupy a VERY small volume in comparison to their container 3.) Particles collide in perfectly elastic collisions, move in straight lines between collisions, and do not attract/repel each other
To solve constant pressure calorimetry problems, you need to:
1.) Pick the correct formula 2.) Plug in the correct values & solve for the unknown 3.) CHECK THE UNITS. Often the answer is requested in kJ/mol. You will have to divide your energy answer by the moles of substance related.
Form of kinetic energy
1.) Thermal 2.) Mechanical 3.) Electrical 4.) Magnetic
Ideal gas laws assume
1.) no attractions between gas molecules 2.) gas molecules do not take up space
100.0 mL sample of 0.300 M NaOH is mixed with a 100.0 mL of 0.300 M HNO3 in a coffee cup calorimeter. If both solutions were initially at 35.00 °C & the temp. of the resulting solution was recorded as 37.00°C, determine ∆T rxn (kJ/mol NaOH) for the neutralization rxn b/w aqueous NaOH & HNO3.
1.) no heat lost 2.) density & heat capacity are the same as H2O qsolution = m*Cs*∆T = m = 200.0 mL = 200.0g (100.0 mL + 100.0 mL) Cs = 4.148 J/g°C ∆T = 37.00 °C - 35.00 °C = 2.00°C qsol = 200 g * 4.184 J/g°C * 2.00°C qsol = 1673 J > - 1.673 kJ/mol (exothermic) 0.300 mol/ 1L * 0.100 L = 0.0300 mol ∆H = -1.673 kJ / 0.0300 mol = -55.76 kJ/mol
For a process at constant pressure, 5275 joules are release. This quantity is equivalent to...
1.261 * 10^3 cal
Determine the final temperature of a gold nugget (mass = 376 g) that starts at 288 K and loses 4.85 kJ of heat to a snowbank when it is lost. The specific heat capacity of gold is 0.128 J/g°C.
187 K
2 CO2(g) + H2O(g) > C2H2(g) + 5/2O2(g) C2H2(g) + 2H2(g) > C2H6(g) ∆H = -94.5 H2O(g) > H2(g) + 1/2 O2(g) ∆H = - 71.2 kJ C2H6(g) + 7/2 O2(g) > 2CO2(g) + 3H2O(g) ∆H = -283 kJ
2 CO2(g) + H2O(g) > C2H2(g) + 5/2O2(g) ∆H = 235 kJ
According to the following thermochemical equation, what mass of Hf (in g) must react in order to produce 690 kJ of energy? Assume excess SiO2. SiO2(2) + 4 HF(g) > SiF4(g) + 2 H2O(l) ∆Hrnx = -184 kJ
300.0 g
If 1.50 kg of H2O at 100°C loses 470.0 kj of heat, what is the final temperature?
460.0 kJ * 100 J/1 kJ = 460000J 470000 = 1500g*4.184J/g°C*∆T ∆T = 460000 J/1500g*4.184J/g°C ∆T = 74.96 °C 100 - 74.96 = 25.04°C
A 12.8 g sample of ethanol (C2H5OH) is burned in a bomb calorimeter with a heat capacity of 5.65 kJ/°C. Using the information below, determine the final temperature of the calorimeter if the initial temperature is 25.0°C. The molar mass of ethanol is 46.07 g/mol. C2H5OH(l) + 3 O2(g) > 2 CO2(g) + 3 H2O(g) ΔH°rxn = -1235 kJ
85.6 °C
What is the specific heat of lead if it takes 96 J to raise the temperature of a 75 g block by 10°C?
96 J = 75g*cs*10°C cs = 96J/75g * 10°C cs = 0.128 J/g°C
An ice cube melting
Endothermic (positive ∆H)
Nail polish remover evaporating after it's spilled on skin
Endothermic rxn (positive ∆H)
Sweat evaporating from skin
Endothermic rxn (positve ∆H)
Gasoline burning within engine
Endothermic rxn (postive ∆H)
Energy exchange
Energy is exchanged between the system and surroundings through either heat exchange or work being done
ΔErxn =
Eproducts - Ereactants
Wood burning in a fire
Exothermic rnx (negative ∆H)
Water freezing in a freezer
Exothermic rxn (negative ∆H)
Give the units of molar heat capacity
J/mole°C
∆T =
T final - T initial
Heat capacity of calorimeter
The heat capacity of the calorimeter is the amount of heat absorbed by the calorimeter for each degree rise in temp. & is called the calorimeter constant. - Ccal, KJ/°C
Diffusion
The spontaneous intermingling of the molecules of one gas with another
Which of the following is TRUE ΔEsys = 423 J? Both the system and the surroundings are gaining 423 J Both the system and the surroundings are losing 423 J The system is gaining 423 J, while the surroundings are losing 423 J The system is losing 423 J, while the surroundings are gaining 423 J None
The system is gaining 423 J, while the surroundings are losing 423 J
Calorimetry
Used to measure thermal energy exchanged between reactions & surroundings
Work
a force acting over a distance - Energy = work = force * distance
State function
a mathematical function whose result only depends on the initial and final conditions, not on the process used
An endothermic reaction has
a positive ∆H, absorbs heat from the surroundings, and feels cold to the touch
Energy
anything that has the capacity to do work
Chemical energy
associated with positions of electrons & nuclei
Thermal energy
associated with temperature
The surrounding area is called a ___ & is usually made of a sealed, insulated container filled with ___
bomb calorimeter water
Potential energy
due to position or composition
Surroundings
everything else with which the system can exchange energy
m
mass of material being heated
Which of the following signs on q and w represent the surroundings that is doing work on the system, as well as gaining heat from the surroundings? q = -, w = - q = -, w = + q = +, w = - q = +, w = + None
q = +, w = +
Which of the following signs on q and w represent a system that is doing work on the surroundings, as well as losing heat to the surroundings q = -, w = + q = +, w = + q = +, w = - q = -, w = - None
q = -, w = -
1.0 kg of H2O 25 °C - 99 °C Takes how much heat input?
q = 1000g*4.18 J/g°C*74°C q = 309,320 J
Exchange of heat energy
q = mass * Cs * ∆T
qrxn = -qrxn=
qrxn = -qsolution -qrxn= qsolution
As the temperature of a gas sample increases, the velocity distribution of the molecules ___
shifts toward higher velocity
cs
specific heat of material (value is a constant & differs with different materials)
If bonds need to be broken to form HIGHER energy bonds in new product molecules...
that excess energy has to be added to the system from the surroundings in an ENDOTHERMIC rxn
If bonds need to be broken to form LOWER energy bonds in new product molecules....
that excess energy has to be released from the system to the surrounding in an EXOTHERMIC rnx
joule (J)
the amount of energy needed to move a 1 kg mass of distance of 1 meter - 1 J = 1 N*m = 1 kg * m2/s2
calorie (cal)
the amount of energy needed to raise the temperature of one gram of water 1 degree celsius
Specific heat capacity
the amount of heat energy required to raise the temperature of one gram of a substance one degree celsius
Molar heat capacity
the amount of heat energy to raise the temperature of one more of a substance 1 degree celsius
Enthalpy
the capacity of a chemical reaction to do non-mechanical work & the capacity to release/absorb heat
Define energy
the capacity to do work
If the final condition has a larger amount of internal energy than the initial condition...
the change in the internal energy will be (+)
If the final condition has a smaller amount of internal energy than the initial condition...
the change in the internal energy will be (-)
Heat
the flow of energy caused by a difference in temperature
Hess's Law
the overall enthalpy change in a reaction is equal to the sum of enthalpy changes for the individual steps in the process
Define work
the result of a force acting through a distance
Internal energy
the total amount of kinetic & potential energy a system possesses
Hess's Law equation
ΔH (rxn) = ∑[ΔH(products)] - ∑[ΔH(reactants)]