Chemical Thermodynamics

Similar documents
Chemical thermodynamics the area of chemistry that deals with energy relationships

Chapter 19. Chemical Thermodynamics. Chemical Thermodynamics

Chapter 19 Chemical Thermodynamics

Chpt 19: Chemical. Thermodynamics. Thermodynamics

Chapter 19 Chemical Thermodynamics

Chapter 19 Chemical Thermodynamics

In previous chapters we have studied: Why does a change occur in the first place? Methane burns but not the reverse CH 4 + 2O 2 CO 2 + 2H 2 O

S = k log W 11/8/2016 CHEM Thermodynamics. Change in Entropy, S. Entropy, S. Entropy, S S = S 2 -S 1. Entropy is the measure of dispersal.

S = k log W CHEM Thermodynamics. Change in Entropy, S. Entropy, S. Entropy, S S = S 2 -S 1. Entropy is the measure of dispersal.

4/19/2016. Chapter 17 Free Energy and Thermodynamics. First Law of Thermodynamics. First Law of Thermodynamics. The Energy Tax.

Chapter 11 Spontaneous Change and Equilibrium

CHEM Thermodynamics. Entropy, S

Chapter 19 Chemical Thermodynamics Entropy and free energy

Chapter 19 Chemical Thermodynamics

Entropy, Free Energy, and Equilibrium

Chapter 19. Spontaneous processes. Spontaneous processes. Spontaneous processes

Spontaneous Change.! Although exothermic processes tend to be spontaneous, spontaneous reactions can be exothermic or endothermic:

Thermodynamics Spontaneity. 150/151 Thermochemistry Review. Spontaneity. Ch. 16: Thermodynamics 12/14/2017

Thermodynamics- Chapter 19 Schedule and Notes

Spontaneity, Entropy, and Free Energy

Chapter Eighteen. Thermodynamics

Thermodynamics. Or, will it happen?

The Direction of Spontaneous Change: Entropy and Free Energy

Thermodynamics Cont. Subtitle

Chemistry Chapter 16. Reaction Energy

Chapter 16. Thermodynamics. Thermochemistry Review. Calculating H o rxn. Predicting sign for H o rxn. Creative Commons License

Free-energy change ( G) and entropy change ( S)

Thermodynamics. Thermodynamically favored reactions ( spontaneous ) Enthalpy Entropy Free energy

Chapter 17. Free Energy and Thermodynamics. Chapter 17 Lecture Lecture Presentation. Sherril Soman Grand Valley State University

Chapter Seventeen Thermodynamics: Spontaneity, Entropy, and Free Energy

I PUC CHEMISTRY CHAPTER - 06 Thermodynamics

Types of Energy Calorimetry q = mc T Thermochemical Equations Hess s Law Spontaneity, Entropy, Gibb s Free energy

Chapter 8 Thermochemistry: Chemical Energy. Chemical Thermodynamics

First Law of Thermodynamics. Example of Spontaneous Rxns. Reversible and Irreversible 8/2/2016

Supplemental Activities. Module: Thermodynamics. Section: Second Law of Thermodynamics Key

7.2. Thermodynamics and Equilibrium. What Conditions Favour a Change? 328 MHR Unit 4 Chemical Systems and Equilibrium

Chapter 19. Chemical Thermodynamics

Thermodynamics. Chem 36 Spring The study of energy changes which accompany physical and chemical processes

1 A reaction that is spontaneous.

Chemical Thermodynamics

Chapter 19 Chemical Thermodynamics Entropy and free energy

General Chemistry I. Dr. PHAN TẠI HUÂN Faculty of Food Science and Technology Nong Lam University. Module 4: Chemical Thermodynamics

II. The Significance of the Signs Property Positive (+) Negative (-)

I. The Nature of Energy A. Energy

Disorder and Entropy. Disorder and Entropy

Exam 1A. 4) Calculate the H 0 rxn in kj for this reaction. a) 6339 b) 5106 c) 775 d) 6535 e) 2909

General Chemistry I Concepts

Ch. 17 Thermochemistry

Section 1 - Thermochemistry

Reaction Rates & Equilibrium. What determines how fast a reaction takes place? What determines the extent of a reaction?

Outline of the Course

Entropy, free energy and equilibrium. Spontaneity Entropy Free energy and equilibrium

Ch 18 Free Energy and Thermodynamics:

Energy Ability to produce change or do work. First Law of Thermodynamics. Heat (q) Quantity of thermal energy

Ch 17 Free Energy and Thermodynamics - Spontaneity of Reaction

Energy Ability to produce change or do work. First Law of Thermodynamics. Heat (q) Quantity of thermal energy

Thermodynamics: Entropy, Free Energy, and Equilibrium

Thermodynamics. 1. Which of the following processes causes an entropy decrease?

Chapter 16. Spontaneity, Entropy and Free energy

CHEMISTRY - CLUTCH CH CHEMICAL THERMODYNAMICS.

Thermochemistry. Energy. 1st Law of Thermodynamics. Enthalpy / Calorimetry. Enthalpy of Formation

Thermodynamics: Free Energy and Entropy. Suggested Reading: Chapter 19

Chemical Thermodynamics

Mr Chiasson Advanced Chemistry 12 / Chemistry 12 1 Unit B: Thermochemical Changes

Thermodynamics. Thermodynamics1.notebook. December 14, Quality vs Quantity of Energy

CHAPTER 11: Spontaneous Change and Equilibrium

Chapter 15 Energy and Chemical Change

Chapter 19. Chemical Thermodynamics

Chemical Thermodynamics. Chapter 18

Chemistry 123: Physical and Organic Chemistry Topic 2: Thermochemistry

Thermodynamics II. Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

Chapter 17 Spontaneity, Entropy, and Free Energy

Chapter 20: Thermodynamics

Reaction Rates & Equilibrium. What determines how fast a reaction takes place? What determines the extent of a reaction?

UNIT 15 - Reaction Energy & Reaction Kinetics. I. Thermochemistry: study of heat in chemical reactions and phase changes

Energy, Heat and Chemical Change

Saturday Study Session 1 3 rd Class Student Handout Thermochemistry

Thermochemistry. Energy and Chemical Change

AP Chemistry Chapter 16 Assignment. Part I Multiple Choice

The reactions we have dealt with so far in chemistry are considered irreversible.

CHEM Introduction to Thermodynamics Fall Entropy and the Second Law of Thermodynamics

ENTHALPY CHANGE CHAPTER 4

CP Chapter 17 Thermochemistry

Chapter 17 Spontaneity, Entropy, and Free Energy

Thermochemistry. Energy (and Thermochemistry) World of Chemistry Chapter 10. Energy. Energy

Thermodynamics. Thermodynamics of Chemical Reactions. Enthalpy change

0. Graphite is thermodynamically less stable that diamond under standard conditions. 1. True 2. False

So far changes in the state of systems that occur within the restrictions of the first law of thermodynamics were considered:

Energy and Chemical Change

CHEMICAL THERMODYNAMICS. Nature of Energy. ΔE = q + w. w = PΔV

Chapter 8 Thermochemistry: Chemical Energy

Unit 7 Kinetics and Thermodynamics

Name AP CHEM / / Collected AP Exam Essay Answers for Chapter 16

5.2 Energy. N Goalby chemrevise.org Lattice Enthalpy. Definitions of enthalpy changes

THERMODYNAMICS I. TERMS AND DEFINITIONS A. Review of Definitions 1. Thermodynamics = Study of the exchange of heat, energy and work between a system

CHAPTER 17 Thermochemistry

Chemistry 2000 Lecture 9: Entropy and the second law of thermodynamics

CHAPTER 12: Thermodynamics Why Chemical Reactions Happen

Chapter 19. Chemical Thermodynamics

Chemical Thermodynamics

Transcription:

Chemical Thermodynamics Overview Everything in the world is a balance of energy, in various forms from biological processes to the rusting of a nail. Two of the most important questions chemists ask are: How fast does the reaction proceed? and How far does it proceed?. These questions were addressed in unit 8 and unit 9,10 & 11 respectively. In truth, the rate of chemical reaction and equilibria is closely tired to energy. In this section we will look at chemical thermodynamics which discusses the relationship between various forms of energy. Spontaneous Processes The first law of thermodynamics states that energy is conserved. In other words energy is neither created nor destroyed in any processes whether that process is a brick falling, a candle burning, or an ice cube melting. Energy can be transferred between a system and the surrounding and can be converted from one form to another, but the total energy of the universe remains constant. The first law of thermodynamics says nothing about how energy moves, just that it must be conserved. A spontaneous process is one that proceeds on its own without any outside assistance. For example at room temperature ice will spontaneously melt. However, the reverse process (freezing) is nonspontaneous. For any chemical reaction that is spontaneous at given conditions, the reverse will be nonspontaneous. Also, because a process is spontaneous doesn t mean that it will take place at an observable rate: it could be explosive or it could be very slow. Finally, a nonspontaneous process doesn t mean it won t happen it just means it won t happen under the current conditions. Predict whether each process is spontaneous or nonspontaneous: (a) Water at 40 C gets hotter when a piece of metal heated to 150 C is added (b) Water at room temperature decomposes into H 2 (g) + O 2 (g) (c) Benzene vapour, C 6 H 6 (g) at a pressure at 1 atm condenses to liquid benzene at the normal boiling point of benzene, 80.1 C

Reversible and Irreversible Processes A reversible process is a specific way in which a system changes its state. In a reversible process, the change occurs in such a way that the system and surroundings can be restored to their original states by exactly reversing the change. In other words, we can restore the system to its original condition with no net change to either the system or its surroundings. An irreversible process is one that cannot simply be reversed to restore the system and its surroundings to their original states. Chemical changes are irreversible processes. For example, if you place a hot object next to a cold one the laws of thermodynamics say that the heat will flow from the hot object to the cold object. You cannot make the reverse happen. This is an irreversible process. Let s imagine a scenario where the above change could be reversible: If two objects are placed side by side with infinitesimally small differences in temperature, so close in temperature that most people would say they are the same temperature. When placed side by side the two objects exchange heat at an infinitely slow rate. This process would be reversible since the change was extremely small and the time it occurred was very large. In short, any change we can observe is happening too fast to be considered reversible. To generalize further, any spontaneous process (any process that occurs without work input) is irreversible. Entropy Knowing that any spontaneous process is irreversible, can we make a prediction about whether a process is spontaneous or not if the process is unfamiliar? To do this we must understand a thermodynamic process called entropy. Entropy is a measure of the randomness of a system. That is, it tells us how much disorder there is in a system. Take a jar of marbles. In the jar the marbles are ordered, the balls are sitting together closely packed. If the jar breaks the marbles will spread out, separating from each other and increase their randomness. This would signal an increase in entropy. Quantitatively, entropy is a state function (like enthalpy) and is a characteristic of the system and the chemicals it contains. In experiment, the temperature of the system changes only by small amounts (with the exception of extremely exothermic processes). We call this an isothermal process. Assuming a process is reversible and the temperature is constant we can show that entropy is the heat change divided by the temperature the process is taking place, as shown to the right. Elemental mercury is a silver liquid at room temperature. Its normal freezing poijnt is 38.9 C and its molar enthalpy of fusion is H fusion = 2.29 kj/mol. What is the entropy of the system when 50.0g of Hg(l) freezes at the normal freezing point?

The Second Law of Thermodynamics As described earlier, the first law of thermodynamics is that energy must always be conserved in any process. Does that mean that entropy must also be conserved? Let s look at this situation by calculating the entropy change of a system including the entropy change of its surroundings when our system is 1 mol of ice melting in the palm of your hand. This process is irreversible. Given the enthalpy of fusion for water is 6.01 kj/mol and that your hand is at bond temperature, 37. Determine the change of entropy of the universe fore the melting of ice described above. So the second law of thermodynamics states that: The molecular Interpretation of Entropy and the Third Law of Thermodynamics Until now we have looked at the large scale setting, but how does Entropy changes we have noted look on the molecular level. The randomness of molecules is actually easy to understand when looking at the different states of matter. A solid has more order than a liquid which has more order than a gas. Ludwig Boltzmann decided to look at individual molecules and describe changes in entropy based on the smallest pieces of matter, Let s take a molecule of water. A single molecule of water can have different orientations: Each configuration is called a microstate, W

Boltzmann described these microstates to better describe the entropy of a system. To him, it made sense to say that the more microstates in a system the greater entropy of that system. He related the connection between entropy, S, and microstates by writing: where k = Boltzmann constant 1.38 x 10-23 J/K So entropy of a system will increase for any change that takes place that increases the number of microstates. If the number of microstates decreases, so will the entropy of the system. So we can make qualitative predictions about a chemical reaction based on our predictions about how the change is system will increase the number of microstates: (1) The entropy of a system increases with increasing temperature. (2) The number of microstates increases with an increase in volume (3) The number of microstates increase with an increase in the number of moles (molecules). The Third Law of Thermodynamics states that the entropy (disorder) of a system approaches 0 J/K as the temperature of the system approaches absolute zero (-273.15 C or 0K). At this point all molecular motion stops so there is only 1 microstate. And there fore the ln (W) = ln (1) = 0. Predict the S for each process, assuming each occurs at constant temperature (a) H 2 O(l) H 2 O(g) (b) Ag +1 (aq) + Cl -1 (aq) AgCl(s) (c) 4 Fe(s) + 3O 2 (g) 2Fe 2 O 3 (s) (d) N 2 (g) + O 2 (g) 2NO(g)

Entropy Changes in Chemical Reactions Chemical reactions all experience changes is disorder. As is the case with enthalpy, there are standard molar entropies (measured in joules per Kelvin). These values are tabulated in Appendix C. you should note a few things about entropy, including some specific differences from enthalpy. 1. Unlike enthalpies of formation, standard molar entropies of elements at the reference temperature of 298K are NOT zero. 2. The standard molar entropies of gases are greater than those of liquids and solids, consistent with our interpretation of experimental observations. 3. Standard molar entropies generally increase with increasing molar mass. 4. Standard molar entropies generally increase with an increasing number of atoms in the formula of a substance. Using Hess s law we can determine the molar entropy change for a chemical process using these values in a similar manner as we did for enthalpy. Calculate the change in the standard entropy of the system, S, for the synthesis of ammonia from N 2 (g) and H 2 (g) at 298K N 2 (g) + 3H 2 (g) 2NH 3 (g)