thermochemistry. specific heat formula c p c p = specific heat q q = energy (heat) lost or gained t...
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Thermochemistry
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Specific Heat Formula
cp = Specific Heat
Q = Energy (heat) lost or gained
T = Temperature change
m = Mass
pcTmQ
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Two Types of Thermal Reactions
• Exothermic: Releases Thermal Energy (heat) sign is –
• Endothermic: Absorbs Thermal Energy (heat)
sign is +
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Exothermic Processes
Reactants Products + energy
Processes in which energy is released as it proceeds, and surroundings become warmer
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Endothermic Processes
Reactants + energy Products
Processes in which energy is absorbed as it proceeds, and surroundings become colder
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Enthalpy = HIn a chemical reaction, Enthalpy (H) is equal to the energy that flows as heat.
(at a constant pressure)
Example:
When 1 mol of methane gas is burned it releases 890 kJ of energy
CH4(g) + 2O2(g) CO2(g) + 2H2O(g) + heat
H = -890kj = exothermic reaction
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Calculate H for a process in which 5.8 g of methane are burned. H = -890kJ per mol CH4
Rxn: CH4(g) + 2O2(g) CO2(g) + 2H2O(g) +heatSolution:
Molar mass of CH4 = 16.04 g / mol
5.8 g CH4 1 mol CH4 = 0.36 mol CH4
16.04 g CH4
0.36 mol CH4 -890kJ = -320 kJ
1 mol CH4
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Calculate H when 12.8 g of sulphur dioxide reacts with excess oxygen to form sulphur trioxide. H = -198.2kJ per mol SO2
Solution:
Molar mass of SO2 = 64.07 g / mol
12.8 g SO2 1 mol SO2 = 0.1998 mol SO2
64.07 g SO2
0.1998 mol SO2 -198kj = -39.6 kJ
1 mol SO2
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Hydrogen peroxide decomposes according to the following thermochemical reaction:
H2O2(l) → H2O(l) + 1/2 O2(g)
ΔH = -98.2 kJ
Calculate the change in enthalpy (ΔH) when 4.00 grams of hydrogen peroxide decomposes.
Calculate the change in enthalpy (ΔH) when 36.00 grams of water are created…
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The reaction that occurs in hand warmers is:
4Fe(s) + 3O2(g) 2Fe2O3(s) + heat
H of reaction = -1652kJ
How much heat is released when 2.5 grams of Fe(s) is reacted with excess oxygen?
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Miller + 2 Stitts LadyGaga - $600 2 Winters + Miller Justin Bieber + $300 Stitt 2 Elvis + Winter - $500
Lady Gaga Justin Bieber + 4 Elvis $_____ ???
Law of Concert Tickets!
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You can add KNOWN equations to solve UNKOWN equations
Law of Concert Tickets = Hess’s Law
FLIP (reverse) the equation – you must FLIP the sign (- +)
MULTIPY / DIVIDE equation – must Multiply / Divide the ΔH!
Two Rules:
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2C(s) + H2(g) ---> C2H2(g) ΔH° = ??? kJ
C2H2(g) + (5/2)O2(g) ---> 2CO2(g) + H2O(l) ΔH° = -1299.5 kJ
C(s) + O2(g) ---> CO2(g) ΔH° = -393.5 kJ
H2(g) + (1/2)O2(g) ---> H2O(l) ΔH° = -285.8 kJ
Example #1: Calculate the enthalpy for this reaction:
Given the following thermo chemical equations:
a) first eq: flip it so as to put C2H2 on the product side b) second eq: multiply it by two to get 2C c) third eq: do nothing.
+1299.5 kJ + (-787 kJ) + (-285.8 kJ) = +226.7 kJ
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C2H2(g) + (5/2)O2(g) ---> 2CO2(g) + H2O(l) ΔH° = -1299.5 kJ
C(s) + O2(g) ---> CO2(g) ΔH° = -393.5 kJ
H2(g) + (1/2)O2(g) ---> H2O(l) ΔH° = -285.8 kJ
2C(s) + H2(g) ---> C2H2(g) ΔH° = ??? kJ
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SrO(s) + CO2(g) ---> SrCO3(s) ΔH = -234 kJ
2SrO(s) ---> 2Sr(s) + O2(g) ΔH = +1184 kJ2SrCO3(s) ---> 2Sr(s) + 2C(s) + 3O2(g) ΔH = +2440 kJ
Example #2: Given the following data:
Find the ΔH of the following reaction:
C(s) + O2(g) ---> CO2(g)
a) first equation - flip itb) second equation - divide by two c) third equation - flip it, divide by two
+234 + (+592) + (-1220) = -394
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SrO(s) + CO2(g) ---> SrCO3(s) ΔH = -234 kJ
2SrO(s) ---> 2Sr(s) + O2(g) ΔH = +1184 kJ2SrCO3(s) ---> 2Sr(s) + 2C(s) + 3O2(g) ΔH = +2440 kJ
Example #2: Given the following data:
Find the ΔH of the following reaction:
C(s) + O2(g) ---> CO2(g)
a) first equation - flip itb) second equation - divide by two c) third equation - flip it, divide by two
+234 + (+592) + (-1220) = -394
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Hess's Law
In a reaction, the change in enthalpy (ΔH)is the same - regardless if the reaction occurs in a single step or in several steps. If a series of reactions are added together, the net change in ΔH is the sum of the enthalpy changes for each step.
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Rules for using Hess's Law
If the reaction is multiplied (or divided) by some factor, Δ H must also be multiplied (or divided) by that same factor.
If the reaction is reversed (flipped), the sign of Δ H must also be reversed.
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Water phase changes & EnergyTemperature remains __________ during a phase change.
constant
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Phase Change DiagramProcesses occur by addition of energy
Processes occur by removal of energy
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Phase Diagram Represents phases as a function of temperature and pressure. Critical temperature: temperature above which the vapor can not be liquefied. Critical pressure: pressure required to liquefy AT the critical temperature. Critical point: critical temperature and pressure (for water, Tc = 374°C and 218 atm).
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Phase Changes
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Effect of Pressure on Boiling PointBoiling Point of Water at Various Locations
Location Feet above sea level
Patm (kPa) Boiling Point (C)
Top of Mt. Everest, Tibet 29,028 32 70
Top of Mt. Denali, Alaska 20,320 45.3 79
Top of Mt. Whitney, California 14,494 57.3 85
Leadville, Colorado 10,150 68 89
Top of Mt. Washington, N.H. 6,293 78.6 93
Boulder, Colorado 5,430 81.3 94
Madison, Wisconsin 900 97.3 99
New York City, New York 10 101.3 100
Death Valley, California -282 102.6 100.3
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Phase Diagram Represents phases as a function of temperature and pressure. Critical temperature: temperature above which the vapor can not be liquefied. Critical pressure: pressure required to liquefy AT the critical temperature. Critical point: critical temperature and pressure (for water, Tc = 374°C and 218 atm).
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Phase changes by Name
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Water
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Carbon dioxidePhase
Diagram for
Carbondioxide
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CarbonPhase
Diagram for
Carbon
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Phase Diagram for Sulfur
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Reaction Pathway
• Shows the change in energy during a chemical reaction
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Exothermic Reaction• reaction that
releases energy
• products have lower PE than reactants
2H2(l) + O2(l) 2H2O(g) + energy
energyreleased
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Endothermic Reaction• reaction that
absorbs energy
• reactants have lower PE than products
2Al2O3 + energy 4Al + 3O2
energyabsorbed
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Latent Heat of Phase Change
Molar Heat of Fusion
The energy that must be absorbed in order to convert one mole of solid to liquid at its melting point.
The energy that must be removed in order to convert one mole of liquid to solid at its freezing point.
Molar Heat of Solidification
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Latent Heat of Phase Change #2Molar Heat of Vaporization
The energy that must be absorbed in order to convert one mole of liquid to gas at its boiling point.
The energy that must be removed in order to convert one mole of gas to liquid at its condensation point.
Molar Heat of Condensation
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Latent Heat – Sample ProblemProblem: The molar heat of fusion of water is6.009 kJ/mol. How much energy is needed to convert 60
grams of ice at 0C to liquid water at 0C?
Massof ice
MolarMass ofwater
Heatof
fusion
kiloJoulesOHmol
kJ
OHg
OHmolOHg20
1
009.6
02.18
160
22
22
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Heat of Solution
Substance
Heat of Solution (kJ/mol)
NaOH -44.51
NH4NO3 +25.69
KNO3 +34.89
HCl -74.84
The Heat of Solution is the amount of heat energy absorbed (endothermic) or released (exothermic) when a specific amount of solute dissolves in a solvent.
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Energy is the capacity to do work
• Thermal energy is the energy associated with the random motion of atoms and molecules
• Chemical energy is the energy stored within the bonds of chemical substances
• Nuclear energy is the energy stored within the collection of neutrons and protons in the atom
• Electrical energy is the energy associated with the flow of electrons
• Potential energy is the energy available by virtue of an object’s position 6.1
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Thermochemistry is the study of heat change in chemical reactions.
The system is the specific part of the universe that is of interest in the study.
open
mass & energyExchange:
closed
energy
isolated
nothing
SYSTEMSURROUNDINGS
6.2
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Exothermic process is any process that gives off heat – transfers thermal energy from the system to the surroundings.
Endothermic process is any process in which heat has to be supplied to the system from the surroundings.
2H2 (g) + O2 (g) 2H2O (l) + energy
H2O (g) H2O (l) + energy
energy + 2HgO (s) 2Hg (l) + O2 (g)
6.2
energy + H2O (s) H2O (l)
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Enthalpy (H) is used to quantify the heat flow into or out of a system in a process that occurs at constant pressure.
DH = H (products) – H (reactants)
DH = heat given off or absorbed during a reaction at constant pressure
Hproducts < Hreactants
DH < 0Hproducts > Hreactants
DH > 0 6.3
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Thermochemical Equations
H2O (s) H2O (l)DH = 6.01 kJ
Is DH negative or positive?
System absorbs heat
Endothermic
DH > 0
6.01 kJ are absorbed for every 1 mole of ice that melts at 00C and 1 atm.
6.3
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Thermochemical Equations
CH4 (g) + 2O2 (g) CO2 (g) + 2H2O (l)DH = -890.4 kJ
Is DH negative or positive?
System gives off heat
Exothermic
DH < 0
890.4 kJ are released for every 1 mole of methane that is combusted at 250C and 1 atm.
6.3
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H2O (s) H2O (l)DH = 6.01 kJ
• The stoichiometric coefficients always refer to the number of moles of a substance
Thermochemical Equations
• If you reverse a reaction, the sign of DH changes
H2O (l) H2O (s)DH = -6.01 kJ
• If you multiply both sides of the equation by a factor n, then DH must change by the same factor n.
2H2O (s) 2H2O (l)DH = 2 x 6.01 = 12.0 kJ
6.3
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H2O (s) H2O (l)DH = 6.01 kJ
• The physical states of all reactants and products must be specified in thermochemical equations.
Thermochemical Equations
6.3
H2O (l) H2O (g)DH = 44.0 kJ
How much heat is evolved when 266 g of white phosphorus (P4) burn in air?
P4 (s) + 5O2 (g) P4O10 (s) DH = -3013 kJ
266 g P4
1 mol P4
123.9 g P4
x3013 kJ1 mol P4
x = 6470 kJ
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The specific heat (s) of a substance is the amount of heat (q) required to raise the temperature of one gram of the substance by one degree Celsius.The heat capacity (C) of a substance is the amount of heat (q) required to raise the temperature of a given quantity (m) of the substance by one degree Celsius.
C = ms
Heat (q) absorbed or released:
q = msDt
q = CDt
Dt = tfinal - tinitial
6.4
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How much heat is given off when an 869 g iron bar cools from 940C to 50C?
s of Fe = 0.444 J/g • 0C
Dt = tfinal – tinitial = 50C – 940C = -890C
q = msDt= 869 g x 0.444 J/g • 0C x –890C= -34,000 J
6.4
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Constant-Volume Calorimetry
No heat enters or leaves!
qsys = qwater + qbomb + qrxn
qsys = 0
qrxn = - (qwater + qbomb)
qwater = msDt
qbomb = CbombDt
6.4
Reaction at Constant V
DH ~ qrxn
DH = qrxn
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Constant-Pressure Calorimetry
No heat enters or leaves!
qsys = qwater + qcal + qrxn
qsys = 0
qrxn = - (qwater + qcal)
qwater = msDt
qcal = CcalDt
6.4
Reaction at Constant PDH = qrxn
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Prentice-Hall © 2002 General Chemistry: Chapter 7 Slide 49 of 50
Terminology
• Energy, U– The capacity to do work.
• Work– Force acting through a distance.
• Kinetic Energy– The energy of motion.
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Prentice-Hall © 2002 General Chemistry: Chapter 7 Slide 50 of 50
Energy
• Kinetic Energy
ek =
12 mv2 [ek ]
=
kg m2
s2 = J
w = Fd [w ] =
kg ms2 = Jm
• Work
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Prentice-Hall © 2002 General Chemistry: Chapter 7 Slide 51 of 50
Energy• Potential Energy
– Energy due to condition, position, or composition.
– Associated with forces of attraction or repulsion between objects.
• Energy can change from potential to kinetic.
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Prentice-Hall © 2002 General Chemistry: Chapter 7 Slide 52 of 50
Energy and Temperature
• Thermal Energy– Kinetic energy associated with random molecular
motion.– In general proportional to temperature.– An intensive property.
• Heat and Work– q and w.– Energy changes.
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Prentice-Hall © 2002 General Chemistry: Chapter 7 Slide 53 of 50
Heat
Energy transferred between a system and its surroundings as a result of a temperature difference.
• Heat flows from hotter to colder.– Temperature may change.– Phase may change (an isothermal process).
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Prentice-Hall © 2002 General Chemistry: Chapter 7 Slide 54 of 50
Units of Heat
• Calorie (cal)– The quantity of heat required to change the
temperature of one gram of water by one degree Celsius.
• Joule (J)– SI unit for heat
1 cal = 4.184 J
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Prentice-Hall © 2002 General Chemistry: Chapter 7 Slide 55 of 50
Heat Capacity
• The quantity of heat required to change the temperature of a system by one degree.
– Molar heat capacity.• System is one mole of substance.
– Specific heat capacity, c.• System is one gram of substance
– Heat capacity• Mass specific heat.
q = mcT
q = CT