Download - Chapter 19: Chemical Thermodynamics
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Chapter 19: Chemical Thermodynamics
Tyler BrownHailey Messenger
Shiv PatelAgil Jose
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19.1 Spontaneous Processes
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19.1 Spontaneous Processes
Spontaneous Process:• A process that proceeds on its own without any
outside assistance• Occurs in a definite direction
“Processes that are spontaneous in one direction are nonspontaneous in the other”
(Pg 805 Brown and LeMay)
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19.1 Spontaneous Processes
Reversible Process:• A process in which the system is changed in a way
that the system and surroundings can be restored to their original state by exactly reversing the change (can be completely restored to original condition)
• Reversible processes reverse direction whenever an infinitesimal change is made in some property of the system
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19.1 Spontaneous Processes
Irreversible Process:• Cannot be reversed to return system and
surroundings to original state
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19.1 Spontaneous Processes
Isothermal Process:• A process with a constant temperature
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19.1 Spontaneous Processes
• First Law of Thermodynamics: Energy is conserved
• “Physical and chemical processes have a directional character” (Pg 804)
• I.e. Sodium and Chlorine come together on their own to make NaCl, but it does not decompose of its own accord.
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19.1 Spontaneous Processes
• Experimental conditions help to determine if a process is spontaneous
• I.e. When the temperature > 0°C in ordinary atmospheric pressure, ice melting is spontaneous.
» In these conditions, liquid water turning in to ice is not spontaneous
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19.1 Spontaneous Processes
• Entropy: The ratio of heat delivered to the temperature at which it is delivered
• “A reversible change produces the maximum amount of work that can be achieved by the system on the surroundings (wrev= wmax)” (Page 807)
• All spontaneous processes are IRREVERSIBLE
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19.1 Spontaneous Processes
Tell whether or not the following process is spontaneous
Ice melts at -1 degree Celsius
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19.1 Spontaneous Processes
Tell whether or not the following process is spontaneous
Ice melts at -1 degree Celsius
This would not be spontaneous because Ice does not melt under 0 degrees Celsius. This reaction would be spontaneous in the reverse reaction
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19.1 Spontaneous Processes
• 19.1 Problems: 7-18
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19.2 Entropy and the Second Law of Thermodynamics
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19.3 The Molecular Interpretation of Entropy
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Molecular motion
• Translational Motion – entire molecule moves in one direction (like throwing a baseball)
• Vibrational Motion – atoms in the molecule periodically move toward and away from one another
• Rotational Motion – molecules spin like a top
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What is Statistical Thermodynamics?
• It’s the use of tools of statistics and probability to provide the link between macroscopic and microscopic worlds
• We molecules in bulk in a microstate: a single possible arrangement of the positions and kinetic energies of gas molecules in a specific thermodynamic state
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So what equation do we use?
• Boltzmann created this beautiful equation:
S = k lnW
K is Boltzmann’s constant which is: 1.38 x 10-23J/K
-This means entropy is the measure of how many microstates are associated with a particular macroscopic state
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Relationship between microstates and entropy
• The more microstates, the more entropy• Increasing volume, temperature, and
number of molecules increases entropy due to larger number of microstates
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GENERALLY SPEAKING
Entropy increases when:- Gases are formed from either solids or
liquids- Liquids or solutions are formed from solids- The number of gas molecules increases
during a chemical reaction
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The Third Law of Thermodynamics
• The entropy of a pure crystalline substance at absolute zero is zero
S(0 K) = 0
- Makes sense because when there is no molecular motion (temp is 0 K), there is only ONE microstate
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Trends
• Sharp increase of entropy at melting points• Sharp increase of entropy at boiling points
Entropy of solids < Entropy of liquids < Entropy of gas
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Example
• What will the sign of change of entropy be for the following reactions?
2Na(s) + Cl2 (g) 2NaCl (s)
2H2 (g) + O2 (g) 2H2O (l)
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Answers • Because of Boltzmann’s equation, we know that
the more particles there are in a system, the more microstates there are, so the more entropy there is, so:
• The reaction to form NaCl has a negative sign for change in entropy, since there are less particles after the reaction
• The reaction to form water also has a negative sign for change in entropy since there are less particles
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Example
• In a chemical reaction two gases combine to form a solid. What do you expect for the sign of change in S? For which of the processes does the entropy of the system increase? A)The melting of ice cubes at -5 degrees Celsius and 1 atm pressure B) dissolution of sugar in a cup of hot coffee C) the reaction of nitrogen atoms to form N2
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Answer• Entropy decreases when two gases form a
solid, so negative sign• A) Positive because the ice is melting from a
structured solid to unstructured liquid• B) Positive because the sugar went from
being structured solids to numerous separated particles
• C) Negative, there is a huge decrease in the number of gas particles (by 1/2 to be exact)
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Practice, practice, practice!
• Page 838 #’s 19.27 – 19.40• A closer look on page 810
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19.4 Entropy Changes in Chemical Reactions
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How do we do it?
• We can’t measure change in entropy for a reaction, but we CAN find the absolute value of the entropy for many substances at any temperature
• Standard molar entropies are denoted by S° (pronounced S knot) for any pure substance in their standard state at 1 atm
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Observations on Standard Entropy
• Standard molar entropies (SME) of elements at reference temperature 298 K are not zero
• SME of gases greater than liquids• SME generally increase with molar mass• SME generally increase with number of
atoms in molecular formula
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So what’s the equation we use?
ΔS° = ΣnS(products) – ΣnS(reactants)
In englishChange in entropy equals sum of entropies
of products minus the sum of entropies of reactants
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Entropy Changes in the Surroundings
• The change in entropy of the surroundings will depend on how much heat is absorbed or given off by the system
• Isothermal process equation:
ΔSsurr=-qsys/T
- At constant pressure, qsys is the enthalpy change of the system, ΔH
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Example
• Calculate change in standard entropy for the following reaction
• 2Na(s) + Cl2 (g) 2NaCl (s)
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Answer• 1. The standard entropy change is equal to the standard entropy of
products minus the reactants
2. So we must first find the standard entropy of the products(using a standard entropy table), and multiply them by the number of moles in the reaction
Standard entropy of NaCl = 72.1 J/K-mol, so 2(72.1)= 144.2
3. Then we find the standard entropy of reactantsStandard entropy of Na = 51.2 J/K-mol, so 2(51.2)= 102.4 J/K-molStandard entropy of Cl2 = 223.1 J/K-mol, 223.1 J/K-mol
4. Now we subtract product and reactants144.2 J/K-mol – (102.4 J/K-mol + 223.1 J/K-mol) = - 181.3 J/K-mol
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Example
• Cyclopropane and propylene isomers both have the formula C3H6. Based on the molecular structures shown, which of these isomers would you expect to have the higher standard molar entropy at 25 degrees Celsius?
Cyclopropane Propylene
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Answer
• Propylene because it is much less organized compared to Cyclopropane
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We love to practice!
• Page 839 #’s 19.41 – 19.48• Example on page 821, figure 19.5
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19.5 Gibbs Free Energy
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19.5 Gibbs Free Energy
• Standard Free Energies of Formation: Used to calculate standard free-energy change for chemical processes
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19.5 Gibbs Free Energy
• Equation for Standard Free-Energy Change:
ΔG° = ΣnΔG°f (products) - ΣmΔG°f
(reactants)
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19.5 Gibbs Free Energy
• G = H – TS
• T is the absolute temperature.
• The change in free energy of a system (ΔG) is given by: ΔG= ΔH – TΔS
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19.5 Gibbs Free Energy
• If ΔG is negative, the reaction is spontaneous
• If ΔG is zero, then reaction is at equilibrium
• If ΔG is positive, the forward reaction is not spontaneous, but the reverse reaction is.
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19.5 Gibbs Free Energy
• For a certain chemical reaction, ΔH = -35.4 kJ and ΔS = - 85.5 J/K. Calculate ΔG for the reaction at 298 K.
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19.5 Gibbs Free Energy
• For a certain chemical reaction, ΔH = -35.4 kJ and ΔS = - 85.5 J/K. Calculate ΔG for the reaction at 298 K (19.51 C)
ΔG = ΔH –TΔSΔG = - 35.4 kJ – (298K)(-85.5 J/K)ΔG = - 35.4 kJ + 25500 JΔG = -35.4 kJ + 25.5 kJΔG = -9.9 kJ
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19.5 Gibbs Free Energy
• 19.5 Problems: 49 -70
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19.6 Free Energy and Temperature
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19.6 Free Energy and Temperature
•The equation ΔG=ΔH+(–TΔS) in which ΔH is the enthalpy term and –TΔS is the entropy term, can be used to demonstrate how free energy is affected by the change in temperature.•The value of –TΔS depends directly on the absolute temperature, T, ΔG will vary with the temperature.
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19.6 Free Energy and Temperature
• T is a positive number at all temperatures other than absolute zero.
• Both the enthalpy and entropy can be either positive or negative.
• When ΔS is positive, which means greater randomness than the original state, then the TΔS is negative. When the ΔS is negative, then the TΔS is positive.
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19.6 Free Energy and Temperature
• ΔG will always be negative when the process is spontaneous, and the opposite is true when the process is not spontaneous.
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19.6 Free Energy and Temperature
• H2O(s) → H2O(l) ΔH>0 ΔS>0• This process is endothermic, meaning the
ΔH is positive. Entropy also increases with this process, meaning that ΔS is positive as well, which makes –TΔS a negative value. This means that the –TΔS term dominates, making ΔG negative. A negative ΔG means that this process is spontaneous at T>0ºC
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19.6 Free Energy and Temperature
• Calculate ΔG for 2NO2(g) → N2O4(g) at 298K using appendix C.
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19.6 Free Energy and Temperature
• ΔH 2NO2(g) → N2O4(g) = -58.02 kJ/mol
• ΔS 2NO2(g) → N2O4(g) = -175.79 J/K•
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19.6 Free Energy and Temperature
• ΔGº =• -58.02kJ – (298K)(-175.79J/K)(1kJ/1000J)• -58.02kJ – (298K)(-0.176kJ/K)• -58.02kJ – (-52.45kJ)• ΔGº = -5.57kJ• This means that at 298K, • 2NO2(g) → N2O4(g) is a spontaneous reaction.
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19.6 Free Energy and Temperature
• Textbook problems: chapter 19, 65,66,79. 80, and 87
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19.7 Free Energy and the Equilibrium Constant
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Most reactions occur in nonstandard conditions
• To find the free energy in nonstandard reactions, we use the standard free energy change to calculate
ΔG = ΔG° + RT ln(Q)R is ideal gas constant = 8.314 J/mol-KT is absolute temperatureQ is reaction quotient for that particular
mixture of interest
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Some more info
• At equilibrium ΔG = 0• Q = equilibrium constant K
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Trends
• The more negative ΔG°, is the larger K is• The more positive ΔG° is, the smaller K is
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Example
• 2CO(g) + O2 (g) 2CO2 (g)
• Calculate the change in free energy for the above reaction at 298K, for a reaction mixture that consists of 1.0 atm O2 , 2.0 atm CO , and 0.75 atm CO2
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Answer1. First we must find Q in order to use the equation provided
earlier. So we solve for the reaction quotient:Q=(PCO2 )2 / (PCO)2(PO2 )=(.75 atm)2 / (2.0 atm)2 (1.0 atm) = .14atm
2. Now calculate standard change in free energy for reaction using tables
Products – Reactants, so 2(-394.4kJ/mol) – (2(-137.2kJ/mol) + 0)Change in standard free energy is -514.4 kJ/mol3. Now we can finally use ΔG = ΔG° + RT ln(Q) ΔG = (-514.4 kJ/mol) + (8.314 J/mol-K)(298 K) (1 kJ/1000J)ln(.14)
= (-514.4 kJ/mol) – 4.871 kJ/mol = -519.271 = - 520 kJ/mol
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Practice Problems
• Page 841• Problems 19.71 – 19.95
• You can find answers on pages A-24 thru A-25
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