Chem 401 Unit 1 (Kinetics & Thermo) Review

Similar documents
Chem 401 Unit 1 (Kinetics & Thermo) Review

CHEMISTRY - CLUTCH CH.13 - CHEMICAL KINETICS.

Advanced Chemistry Practice Problems

What we learn from Chap. 15

AP CHEMISTRY CHAPTER 12 KINETICS

Thermodynamics. Thermodynamics of Chemical Reactions. Enthalpy change

Chapter 12. Chemical Kinetics

Ch 13 Rates of Reaction (Chemical Kinetics)

Unit - 4 CHEMICAL KINETICS VSA QUESTIONS (1 - MARK QUESTIONS) (aq) as product for the reaction : 5 Br (aq) + Br(aq) + 6H + (aq) 3 Br 2

A proposed mechanism for the decomposition of hydrogen peroxide by iodide ion is: slow fast (D) H 2 O

CHEMISTRY 102 FALL 2009 EXAM 2 FORM B SECTION 501 DR. KEENEY-KENNICUTT PART 1

Bonus Final Exam 3. 1 Calculate the heat of reaction,δh 0 rxn, for the following reaction as written at 298 K: g 2H 2 CH 4. g CF 4.

temperature begins to change noticeably. Feedback D. Incorrect. Putting an object on a hot plate will always cause the temperature to increase.

B. Activation Energy: Ea

Practice Test: Energy and Rates of Reactions

concentrations (molarity) rate constant, (k), depends on size, speed, kind of molecule, temperature, etc.

Chapter 12. Chemical Kinetics

CHAPTER 12 CHEMICAL KINETICS

CHEM Chapter 14. Chemical Kinetics (Homework) Ky40

CHAPTER 13 (MOORE) CHEMICAL KINETICS: RATES AND MECHANISMS OF CHEMICAL REACTIONS

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

MCAT General Chemistry Discrete Question Set 19: Thermochemistry & Thermodynamics

, but bursts into flames in pure oxygen.

Chapter 14 Chemical Kinetics

Homework 11 - Second Law & Free Energy

Chapter 13 Kinetics: Rates and Mechanisms of Chemical Reactions

Factors That Affect Rates. Factors That Affect Rates. Factors That Affect Rates. Factors That Affect Rates

Unit 12. Thermochemistry

AP Chem Chapter 14 Study Questions

Second Law of Thermodynamics

Chem 401 Unit 1 Exam: Thermodynamics & Kinetics (Nuss: Spr 2018)

CHEMISTRY 102 FALL 2010 EXAM 2 FORM B SECTION 501 DR. KEENEY-KENNICUTT PART 1

OAT General Chemistry Problem Drill 15: Thermochemistry & Thermodynamics

Chapter 14. Chemical Kinetics

AP CHEMISTRY NOTES 7-1 KINETICS AND RATE LAW AN INTRODUCTION

Answers to Unit 4 Review: Reaction Rates

U N I T T E S T P R A C T I C E

Entropy. Spontaneity. Entropy. Entropy mol of N 2 at 1 atm or 1 mol of N 2 at atm. process a process that occurs without intervention

Chapter 14 Chemical Kinetics

OCR Chemistry A H432

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

Lecture #13. Chapter 17 Enthalpy and Entropy

Class XI Chapter 6 Thermodynamics Chemistry

Chapter 12. Chemical Kinetics

Chapter Eighteen. Thermodynamics

Chemistry 112, Spring 2007 Prof. Metz Exam 2 Solutions April 5, 2007 Each question is worth 5 points, unless otherwise indicated

Kinetics CHAPTER IN THIS CHAPTER

Chemistry 123: Physical and Organic Chemistry Topic 2: Thermochemistry

Chapter 14: Chemical Kinetics

Homework 07. Kinetics

7/19/2011. Models of Solution. State of Equilibrium. State of Equilibrium Chemical Reaction

Lecture 2. Review of Basic Concepts

Chapter 17.3 Entropy and Spontaneity Objectives Define entropy and examine its statistical nature Predict the sign of entropy changes for phase

General Chemistry I Concepts

Thermochemistry: the study of energy (in the from of heat) changes that accompany physical & chemical changes

Shroud of Turin. Chemical Kinetics. Reaction Rates. Reaction Rates. Reaction Rates. Chemical Kinetics: The Rates of Chemical Reactions

Chem 116 POGIL Worksheet - Week 12 - Solutions Second & Third Laws of Thermodynamics Balancing Redox Equations

Chem 1B Dr. White 1 Chapter 17: Thermodynamics. Review From Chem 1A (Chapter 6, section 1) A. The First Law of Thermodynamics

Chapter 19 Chemical Thermodynamics Entropy and free energy

11/2/ and the not so familiar. Chemical kinetics is the study of how fast reactions take place.

Chemical Kinetics. Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

UNIT-4 CHEMICAL KINETICS CONCEPT

UNIVERSITY OF SIERRA LEONE FOURAH BAY COLLEGE. FIRST EXAMINATION FOR THE DEGREE OF B. Sc. HONOURS LEVEL I SECOND SEMESTER EXAMINATION

CHEMISTRY 102 FALL 2010 EXAM 2 FORM C SECTION 502 DR. KEENEY-KENNICUTT PART 1

CHEMISTRY 202 Hour Exam III. Dr. D. DeCoste T.A (60 pts.) 31 (20 pts.) 32 (20 pts.) 33 (20 pts.) Total (120 pts)

Unit 7 Kinetics and Thermodynamics

Downloaded from

Ch 17 Free Energy and Thermodynamics - Spontaneity of Reaction

Chemical Kinetics -- Chapter 14

2/18/2013. Spontaneity, Entropy & Free Energy Chapter 16. The Dependence of Free Energy on Pressure Sample Exercises

Collision Theory. Unit 12: Chapter 18. Reaction Rates. Activation Energy. Reversible Reactions. Reversible Reactions. Reaction Rates and Equilibrium

2/23/2018. Familiar Kinetics. ...and the not so familiar. Chemical kinetics is the study of how fast reactions take place.

Unit 5: Spontaneity of Reaction. You need to bring your textbooks everyday of this unit.

Exam 2 Solutions. for a gas obeying the equation of state. Z = PV m RT = 1 + BP + CP 2,

Final Exam Review-Honors Name Period

Kinetics - Chapter 14. reactions are reactions that will happen - but we can t tell how fast. - the steps by which a reaction takes place.

1. How much heat is required to warm 400. g of ethanol from 25.0ºC to 40.0ºC?

Practice test Chapter 12 and 13

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

Reaction Rate. Rate = Conc. of A at t 2 -Conc. of A at t 1. t 2 -t 1. Rate = Δ[A] Δt

14.1 Expressing the Reaction Rate

Disorder and Entropy. Disorder and Entropy

CHAPTER 16 REVIEW. Reaction Energy. SHORT ANSWER Answer the following questions in the space provided.

A is the frequency factor (related to the number of collisions)

Thermodynamics. For the process to occur under adiabatic conditions, the correct condition is: (iii) q = 0. (iv) = 0

HEAT, TEMPERATURE, & THERMAL ENERGY. Work - is done when an object is moved through a distance by a force acting on the object.

CHEMISTRY. Chapter 14 Chemical Kinetics

Unit 2: Thermodynamics & Kinetics. Thermochemistry: study of the energy changes that accompany physical or chemical changes in matter

CHE 107 Spring 2018 Exam 2

Chemical Kinetics. System LENGTH: VOLUME MASS Temperature. 1 gal = 4 qt. 1 qt = in 3. 1 L = qt. 1 qt = L

Energy is the capacity to do work

Take home Exam due Wednesday, Aug 26. In class Exam will be the that morning class multiple choice questions.

Calculating Rates of Substances. Rates of Substances. Ch. 12: Kinetics 12/14/2017. Creative Commons License

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

CHAPTER 20 THERMODYNAMICS: ENTROPY, FREE ENERGY, AND THE DIRECTION OF CHEMICAL REACTIONS

Gibbs Free Energy. Evaluating spontaneity

Thermochemistry Lecture

Chapter 14: Chemical Kinetics

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

Contents and Concepts

Transcription:

KINETICS 1. For the equation 2 H 2(g) + O 2(g) 2 H 2 O (g) How is the rate of formation of H 2 O mathematically related to the rate of disappearance of O 2? 1 Δ [H2O] Δ[O 2] = 2 Δt Δt 2. Determine the relative reaction rates of the four substances involved in the following chemical reaction. Place the appropriate numbers in the boxes. 3. For the following reaction, the rate of disappearance of A is equal to -0.084 M/s at the start of the reaction. What are the rates of change for B, C, and D at this time? 2A + B 3C + D Rate of Change of B = M/s Ans: -0.042 Rate of Change of C = M/s Ans: +0.126 Rate of Change of D = M/s Ans: +0.042 4. Based on the graph below, determine the instantaneous rate of change of [x] at 10 seconds. Instantaneous Rate of Change of X = Ans: rise = (0.11M-0.07M) = 0.04M Run = (15s 5s) = 10s Slope = 0.04/10 = 0.004M/s 1

5. Based on the data below, what are the average rates of change of [O 2 ] and [NO 2 ] over the interval 0 to 660 seconds? Time (s) [NO] M [O 2 ] M [NO 2 ] M 0 0.1000 0.01000 0.0000 285 0.0090 0.0095 0.0010 660 0.0080 0.0090 0.0020 1175 0.00070 0.0085 0.0030 Average Rate of Change of O 2 = = (0.0090-0.0100)/(660-0) = -1.5x10-6 M/s Average Rate of Change of NO 2 = = (0.0020-0.0000)/(660-0) = 3.0x10-6 M/s 6. If the rate constant, k=350 s -1 for a certain reaction, what is the overall order for that reaction? First Order 8. The following reaction occurs in the gaseous state. 2 NO (g) + 2 H 2(g) N 2(g) + 2H 2 O (g) The following rate data were obtained. Trial Initial [NO] Initial [H 2 ] Initial rate(m/s) 1 0.20 M 0.20 M 0.060 2 0.20M 0.30 M 0.090 3 0.40M 0.20 M 0.240 (a) Determine the rate law for this reaction (including all exponents & rate constant). Trial 2/Trail 1 conc ratio = 1.5 rate ration = 1.5 H 2 coefficient = 1 Trial 3/Trial 1 conc ration = 2.0 rate ratio = 4 NO coefficient = 2 Using trial 3 data to get k, 0.240 = k(0.40) 2 (0.20) k = 0.240 = 7.5 M -2 s -1 (0.40) 2 (0.20) Rate Law: rate = 7.5 M -2 s -1 [NO] 2 [H 2 ] (b) What is the order or the reaction with respect to: NO? 2 H 2? 1 Overall? 3 (c) What would the initial rate of the reaction be if the initial concentrations were: [NO] = 0.10M [H 2 ] = 0.30 M Rate = 7.5 M -2 s -1 (0.10M) 2 (0.30M) = 0.022 M/s 2

9. Determine the rate constant of the following reaction at 298K, where A (the Arrhenius pre-exponent factor)=1.2x10 12, and Ea=11.6kJ/mol k = Ae Ea/RT NO (g) + O 3(g) NO 2(g) + O 2(g) k = (1.2x10 12 )e [(-11600J)/(8.314J/K mol)(298k)] = 1.1 x 10 10 10. Complete the data table below for the reaction A + B C. Then calculate the slope of the plot of ln k vs 1/T (Arrhenius Plot) and the activation energy of the reaction. Be sure to use unrounded values in your calculations. K (M -1 s -1 ) T (K) Ln k 1/T (K -1 ) 6255 288 8.74114 0.003472 Slope = (9.08602-8.74114) = 0.34488 = -917.2K (0.003096 K -1-0.003472 K -1 ) -0.000376 8831 323 9.08602 0.003096 Ea = (-R)(slope) = (-8.314 J/K mol)(-917.2k) =7.63kJ/mol 11. From the following graph, determine the activation energy and the enthalpy of the reaction. Ea = 25 kj/mol ΔH = -150 kj/mol 12. According to the graph below, about what percentage of the collisions will have sufficient kinetic energy to form products? % (50%) 13. In order for a reaction to occur reactant molecules must: A) collide B) with sufficient energy C) in the correct orientation 3

14. The mechanism for the reaction 3 ClO - ClO 3 - ClO - + ClO - ClO 2 - + Cl - ClO - + ClO 2 - ClO 3 - + Cl - (slow) (fast) Derive the rate law for this reaction: Rate = k[clo - ] 2 + 2 Cl - is 15. Identify the catalyst(s) and/or reaction intermediate(s) in the following reaction mechanism. catalyst(s): NO (g) reaction intermediate(s): NO 2(g), O (g) 16. At a certain temperature, the reaction 2B C + D obeys the rate law: rate = 1.14 x 10-3M -1 s -1 [B] 2 If 5.00 mol of B is initially present in a 1.00 L container at that temperature, how much B is left after 117 seconds? We need to start by recognizing the fact that this reaction follows second order kinetics. From our equation sheet: 1/[A] t = kt + 1/[A] o 1-3 [B] t = (1.14 x 10 )(117) + 1 5.00 [B] t = 1/0.333 = 3.00M = 3.00 mol/l 3.00 mol x 1.00L = 3.00 mol B L for 2 nd order = 0.133 + 0.200 = 0.333 17. Write a rate equation for the following elementary step: BeO 3 - + 2 H + H 2 BrO 3 + Rate = k [BeO 3 - ][ H + ] 2 Coefficients match exponents for elementary steps and elementary reactions. 18. For a given reaction, the concentration of reactant A was doubled and the rate of reaction remained the same. We can conclude that the reaction is what order with respect to A?. zero order 4

THERMODYNAMICS 1. Predict the sign for the following reaction and then calculate the value of ΔS using the information below and compare to your prediction for ΔS. O 2(g) + 2 H 2(g) 2 H 2 O (g) Predicted sign: (-) fewer moles of substance compound S J/mol K O 2(g) 205.0 H 2(g) 130.6 H 2 O (g) 188.7 ΔS = 2(188.7) [(205.0)+2(130.6)] = 377.4-466.2 = -88.8 J/mol K 2. Predict the value of ΔG under the following conditions: A) ΔH negative and ΔS positive X ΔG < 0 ΔG > 0 Cannot predict the sign of ΔG B) ΔH positive and ΔS positive ΔG < 0 ΔG > 0 X Cannot predict the sign of ΔG C) ΔH positive and ΔS negative ΔG < 0 X ΔG > 0 Cannot predict the sign of ΔG D) ΔH negative and ΔS negative ΔG < 0 ΔG > 0 X Cannot predict the sign of ΔG 3. Determine the value of ΔG in kj at 25 C for the following reaction given that ΔS =326.4J/K and ΔH =571.6kJ. 2 H 2 O (l) 2 H 2(g) + O 2(g) 4. Calculate the change in entropy for the following reaction. (Hint use your appendix data / green sheet.) Ca 2+ (aq) + 2 OH - (aq) Ca(OH) 2(s) -53.1-10.90 83.4 ΔS = 83.4 [-53.1 + 2(-10.90] = 83.4 (-74.9) = 158.3 J/K mol 5

5. Will the decomposition of potassium chlorate be spontaneous at low temperatures, high temperatures, or all temperatures? Use values from you appendix/handout. Reaction: 2 KClO 3(s) 2 KCl (s) + 3 O 2(g) ΔH f = -397.7-436.5 0 ΔH rxn = 2(-436.5) 2(-397.7) = -77.6 kj/mol S = 143.1 82.6 205.2 ΔS rxn = [3(205.2) + 2(82.6)]-2(143.1)=+494.6J/mol K Since ΔH rxn is (-), it supports spontaneity. Since ΔS rxn is (+), it supports spontaneity. The reaction is spontaneous at all temperatures! 6. True or False F A) Gases have less entropy than liquids. T B) When solids dissolve they tend to increase in entropy. F C) The greater the moles of solid, the greater the entropy F D) CH 4 (g) has greater entropy than CH 3 -CH 2 -CH 2 -CH 3(g) T E) An endergonic reaction is always non-spontaneous. 6