1) Which of the following is probably true for a solid solute with a highly endothermic heat of solution when dissolved in water? a. The solid has a low.

Slides:



Advertisements
Similar presentations
Entropy Section 16-2.
Advertisements

Thermo-Chemistry Curve Balls
5. Answer the following questions using the information related to reactions X, Y, and Z in the table above. (a) For reaction X, write the expression for.
Entropy and Free Energy Chapter 19. Laws of Thermodynamics First Law – Energy is conserved in chemical processes neither created nor destroyed converted.
Slide 1 of 44 Chapter 19: Spontaneous Change: Entropy and Free Energy.
CAUSES OF CHANGE Order and Spontaneity. Enthalpy and Reactions Some reactions happen easily, but some others do not. Sodium and chlorine readily react.
Chemistry Problems Thermodynamics Blase Ferraris (did these problems for Gangluff) Final Project 1996B and 1997D.
Review Kinetics and Equilibrium Test. Which will occur if a catalyst is added to a rxn mixture? 1. Only the rate of the reverse reaction will increase.
Thermodynamics. Heat and Temperature Thermochemistry is the study of the transfers of energy as heat that accompany chemical reactions and physical changes.
A spontaneous reaction (or favourable change) is a change that has a natural tendency to happen under certain conditions. Eg. The oxidation of iron (rust)
Thermodynamics Chapter 19 Liquid benzene Production of quicklime Solid benzene ⇅ CaCO 3 (s) ⇌ CaO + CO 2.
© 2006 Brooks/Cole - Thomson Some Thermodynamic Terms Notice that the energy change in moving from the top to the bottom is independent of pathway but.
Thermodynamics: Spontaneity, Entropy and Free Energy.
Thermochemistry Study of the transfer of energy in chemical reactions.
Welcome to Chem 1B CLAS with Eric Engel
© 2013 Pearson Education, Inc. Fundamentals of General, Organic, and Biological Chemistry, 7e John McMurry, David S. Ballantine, Carl A. Hoeger, Virginia.
Chemical Thermodynamics: Entropy, Free Energy and Equilibrium Chapter
 Section 1 – Thermochemistry  Section 2 – Driving Force of Reactions.
Thermochemistry.  What is energy?  Energy is the ability to do work or produce heat.  The Law of Conservation of Energy: ◦ This law states that can.
Chapter 17 THERMODYNAMICS. What is Thermodynamics? Thermodynamics is the study of energy changes that accompany physical and chemical processes. Word.
Chemical Thermodynamics Chapter 19 (except 19.7!).
Chapter 16 Reaction Energy
CHEMISTRY Matter and Change
 Section 1 – Thermochemistry  Section 2 – Driving Force of Reactions.
Chemical Thermodynamics. Spontaneous Processes First Law of Thermodynamics Energy is Conserved – ΔE = q + w Need value other than ΔE to determine if a.
Thermodynamics Chapter st Law of Thermodynamics Energy is conserved.  E = q + w.
Chapter 17 Thermochemistry 17.3 Heat in Changes of State
Energy Chapter 16.
Chapter 19 Reaction Rates and Equilibrium. I.Rates of reaction A. Collision Theory 1. rates : measure the speed of any change during a time interval 2.
Wednesday, Nov. 10 th : “A” Day Agenda  Section 10.4: Order and Spontaneity Entropy, Standard Entropy, Gibbs energy  Homework: Sec review, pg.
Unit 13: Thermochemistry Chapter 17 By: Jennie Borders.
THERMODYNAMICS: ENTROPY, FREE ENERGY, AND EQUILIBRIUM Chapter 17.
Thermochem Quick review
ENTHALPY, HESS’ LAW, AND THERMOCHEMICAL EQUATIONS.
Section 18.4 Entropy. What you need to know - Entropy -Gibbs Free Energy -Enthalpy -Calculating Gibbs Free Energy -Determine if a rxn is spontaneous or.
Thermodynamics (Ch 10) 1. One mole of helium in a volume of 1.0 L at 5.0 atm pressure is allowed to expand isothermally into a volume of 2.0 L. Calculate.
Chapter 19: Chemical Thermodynamics Spontaneous processes… …happen without outside help …are “product favored”
Thermochemistry.  What is energy?  Energy is the ability to do work or produce heat.  The Law of Conservation of Energy: ◦ This law states that can.
Topic: Thermodynamics Do Now: packet p.1. Every physical or chemical change is accompanied by energy change  Energy released = _________________  Energy.
Chapter 9 Lecture Basic Chemistry Fourth Edition 9.5 Energy in Chemical Reactions Learning Goal Given the heat of reaction (enthalpy change), calculate.
AP Chapter 19.  Energy can not be created nor destroyed, only transferred between a system and the surroundings.  The energy in the universe is constant.
Chapter 19 Reaction Rates and Equilibrium. I.Rates of reaction A. Collision Theory 1. rates : measure the speed of any change during a time interval 2.
Thermodymanics.  Thermodynamics is a branch of science that focuses on energy changes that accompany chemical and physical changes.
Chapter 18 – Rates of Reactions and Equilibrium Every biological and non-biological chemical reaction in nature eventually reaches a state called equilibrium.
The Driving Forces of Reactions. In chemistry we are concerned with whether a reaction will occur spontaneously, and under what conditions will it occur.
Chapter 15 Energy and Chemical Change Energy Energy can change for and flow, but it is always conserved.
Calorimetry.
Measuring and Expressing Heat Changes Enthalpy The heat content of a substance that has at given temperature and pressure Change in heat content.
THERMODYNAMICS spontaneous reactions. Why do reactions occur? 14 KMnO C 3 H 5 (OH) 3 7 K 2 CO Mn 2 O CO H 2 O.
 Section 1 – Thermochemistry  Section 2 – Driving Force of Reactions.
The Driving Forces of Reactions AP Chemistry. In chemistry we are concerned with whether a reaction will occur spontaneously, and under what conditions.
Created by Lynne Crandall University of Michigan Revised by Mark Kondrak CLA Language Center University of Minnesota Could you put an image here?
Thermodynamics Chapter 15. Part I Measuring Energy Changes.
Unit 11 Thermodynamics Chapter 16. Thermodynamics Definition Definition A study of heat transfer that accompanies chemical changes A study of heat transfer.
Enthalpy The Meaning of Enthalpy. 1. Enthalpy is a state function with the symbol H. H = E + PV E is the internal energy of the system, P is the pressure.
It is impossible to measure enthalpy directly
Entropy and Spontaneity Section 15.2 (AHL). Introduction Entropy can be regarded as a measure of the disorder or dispersal of energy in a system It measures.
Enthalpy, Entropy, and Spontaneity Explained. Review of Enthalpy Change.
Thermodynamics Cartoon courtesy of NearingZero.net.
* Studying energy flow in chemical changes allows us to predict what is possible and what is not. * 1 st Law of Thermodynamics PE tends only to decrease.
3 Enthalpy. Units SI unit = joule 1KJ = 1000J = cal 1st law of Thermodynamics The total energy of the universe is constant i.e energy cannot be.
1 Calorimetry (4-2). Calorimetry Calorimetry - the accurate and precise measurement of heat change for chemical and physical processes. The device used.
Entropy Entropy, S, is the quantitative measure of the degree of disorder in a system. Entropy is ‘a measure of disorder’ or ‘the amount of randomness’
Chemical Thermodynamics First Law of Thermodynamics You will recall from earlier this year that energy cannot be created nor destroyed. Therefore, the.
Chapter 15 Energy and Chemical Change Section 15.1 Energy Section 15.2Heat Section 15.3Thermochemical Equations Section 15.4 Calculating Enthalpy Change.
AP Chemistry Chapter 5 and 19 Jeopardy Jennie L. Borders.
IIIIIIIVV I. Enthalpy Ch. 5 – Thermochemistry. A. Reaction Energy (Chp. #2) n Heat ( q ) – Units: J (joules)  Total amount of thermal energy  heat or.
 Spontaneous reactions are reactions, that once started, continues by itself without further input of energy from the outside.  If a reaction is spontaneous.
ENERGY OF REACTIONS Entropy, Enthalpy, and Gibb’s Free Energy.
Thermodynamics Chapter Spontaneous Processes – process that occurs without any outside intervention, the internal energy alone determines if.
Presentation transcript:

1) Which of the following is probably true for a solid solute with a highly endothermic heat of solution when dissolved in water? a. The solid has a low lattice energy. b. As the solute dissolves, the temperature of the solution increases. c. The resulting solution is ideal. d. The solid is more soluble at higher temperatures. e. The solid has a high energy of hydration.

D

2). Which of the following reactions has the largest positive value of ΔS per mole of Cl2. a. H2(g) + Cl2(g) --> 2 HCl(g) b. C12(g) + 2 O2(g) --> Cl2O(g) c. Mg(s) + Cl2(g) --> MgCl2(s) d. 2 NH4Cl(s) --> 4 H2(g) + Cl2(g) e. Cl2(g) --> 2 Cl(g)

D

3). Which of the following must be true for a reaction that proceeds spontaneously from initial standard state conditions? a. ΔG° > 0 and Keq > 1 b. ΔG° > 0 and Keq < 1 c. ΔG° < 0 and Keq > 1 d. ΔG° < 0 and Keq < 1 e. ΔG° = 0 and Keq = 1

C

4) H2O(s) --> H2O(l) When ice melts at its normal melting point, 273.16 K and 1 atmosphere, which of the following is true for the process shown above? a. DH < 0, DS > 0, DV > 0 b. DH < 0, DS < 0, DV > 0 c. DH > 0, DS < 0, DV < 0 d. DH > 0, DS > 0, DV >0 e. DH > 0, DS > 0, DV < 0

E

5) CH4(g) + 2 O2(g) --> CO2(g) + 2 H2O(l) ΔHf°CH4 = –889.1 kJ ΔHf°H2O(l) = –285.8 kJ/mol ΔHf°CO2(g) = –393.3 kJ/mol What is the standard heat of formation of methane, ΔHf°CH4(g), as calculated from the data above? (A) –210.0 kJ/mole (D) 75.8 kJ/mole (B) –107.5 kJ/mole (E) 210.0 kJ/mole (C) –75.8 kJ/mole

c

6) H2(g) + 1/2 O2(g) --> H2O(l) ΔH° = –286 kJ 2 Na(s) + 1/2 O2(g) --> Na2O(s) ΔH°= –414 kJ Na(s) + 1/2 O2(g) + 1/2 H2(g) --> NaOH(s) ΔH°= –425 kJ Based on the information above, what is the standard enthalpy change for the following reaction? Na2O(s) + H2O(l) --> 2 NaOH(s) A) –1,125 kJ (B) –978 kJ (C) –722 kJ (D) –150 kJ (E) +275 kJ

D

7) For which of the following processes would ΔS have a negative value? I. 2 Fe2O3(s) --> 4 Fe(s) + 3 O2(g) II. Mg2+ + 2 OH– --> Mg(OH)2(s) III. H2(g) + C2H4(g) --> C2H6(g) (A) I only (B) I and II only (C) I and III only (D) II and III only (E) I, II, and III

D

8) N2(g) + 3 H2(g) --> 2 NH3(g) The reaction indicated above is thermodynamically spontaneous at 298 K, but becomes nonspontaneous at higher temperatures. Which of the following is true at 298 K? (A) ΔG, ΔH, and ΔS are all positive. (B) ΔG, ΔH. and ΔS are all negative. (C) ΔG and ΔH are negative, but ΔS is positive. (D) ΔG and ΔS are negative, but ΔH is positive. (E) ΔG and ΔH are positive, but ΔS is negative.

B

1997 D For the gaseous equilibrium represented below, it is observed that greater amounts of PCl3 and Cl2 are produced as the temperature is increased. PCl5(g) ® PCl3(g) + Cl2(g) (a) What is the sign of DS° for the reaction? Explain. (b) What change, if any, will occur in DG° for the reaction as the temperature is increased? Explain your reasoning in terms of thermodynamic principles. (c) If He gas is added to the original reaction mixture at constant volume and temperature, what will happen to the partial pressure of Cl2? Explain. (d) If the volume of the reaction mixture is decreased at constant temperature to half the original volume, what will happen to the number of moles of Cl2 in the reaction vessel? Explain.

1996 B C2H2(g) + 2 H2(g)  C2H6(g) Information about the substances involved in the reaction represented above is summarized in the following tables. Substance S° (J/molK) DH°f (kJ/mol) C2H2(g) 200.9 226.7 H2(g) 130.7 0 C2H6(g) xx -84.7 (a) If the value of the standard entropy change, DS°, for the reaction is -232.7 joules per moleKelvin, calculate the standard molar entropy, S°, of C2H6 gas. (b) Calculate the value of the standard free-energy change, DG°, for the reaction. What does the sign of DG° indicate about the reaction above? (c) Calculate the value of the equilibrium constant, K, for the reaction at 298 K.

(

1998 B C6H5OH(s) + 7 O2(g)  6 CO2(g) + 3 H2O(l) When a 2.000-gram sample of pure phenol, C6H5OH(s), is completely burned according to the equation above, 64.98 kilojoules of heat is released. Use the information in the table below to answer the questions that follow. Substance Standard Heat of Formation Absolute Entropy DH°C at 25°C (kJ/mol) , S°, at 25°C(J/mol K) C(graphite) 0.00 5.69 CO2(g) -393.5 213.6 H2(g) 0.00 130.6 H2O(l) -285.85 69.91 O2(g) 0.00 205.0 C6H5OH(s) ? 144.0 (a) Calculate the molar heat of combustion of phenol in kilojoules per mole at 25°C. (b) Calculate the standard heat of formation, DH°, of phenol in kilojoules per mole at 25°C. (c) Calculate the value of the standard free-energy change, DG°, for the combustion of phenol at 25°C. (d) If the volume of the combustion container is 10.0 liters, calculate the final pressure in the container when the temperature is changed to 110.°C. (Assume no oxygen remains unreacted and that all products are gaseous.)