a) Write the reaction that occurs (pay attention to and label ends correctly) 5 AGCTG CAGCT > 5 AGCTG 3 3 TCGAC 5
|
|
- Naomi Holt
- 5 years ago
- Views:
Transcription
1 Chem 315 Applications Practice Problem Set 1.As you learned in Chem 315, DNA higher order structure formation is a two step process. The first step, nucleation, is entropically the least favorable. The second step, zippering, caused by the interactions of nearest neighbors, is rapid. The overall folding process 2sS à ds can be considered a two part process 2sS à NsS à ds where NsS is the nucleated intermediate Consider the folding of the following short sequence AGCTG with its compliment. a) Write the reaction that occurs (pay attention to and label ends correctly) 5 AGCTG CAGCT > 5 AGCTG 3 3 TCGAC 5 strand 1 + strand > double strand b) Express the free energy of the folding mathematically (equation) DG o folding = DG o ds (DG o s1 + DG o s2) c) Given the data in the table provided calculate the ΔG o, ΔH o, and ΔS o for the formation of the double stranded sequence. The folding process is two step initiation (nucleation) and H bond formation (zippering) therefore DG overall can be broken down into a broad two step process and the zippering step can be further broken down into formation of each H bond H bonding is free energy favorable nucleation is not Since this this strand does have at least one CG pair from the table the nucleation value is 1.8 kcal/mol The sum of the hydrogen bond values are for AG GC CT and TG (leading strand) = kcal/mol overall = kcal/mol (highly favorable) Likewise the DH o is kcal/mol and the ds o is cal/molk The entropy is unfavorable as expected and this interaction is enthalpy driven.
2 d) Write the equilibrium constant expression and calculate the value of the equilibrium constant at room temperature Keq = ds/ss 2 At 298 (values in the table used for part c) DG o folding = - RTlnKeq cal/mol = 1.985cal/mol K (298 K) lnkeq Keq = 3958 (products highly favored as expected by DG<0) e) Given an initial single strand concentration of 0.1mM, calculate the equilibrium concentrations of the single strands and double strands. Keq = ds/ss = x/ (0.0001M- x) 2 solve quadratic or recognize that given the large equilibrium constant the concentration of product will essentially be 0.1 mm and the reactants 0.
3 2. Draw a reaction coordinate diagram for enzyme catalyzed single substrate reaction that obeys the Michaelis- Menten Model. Label axes, all components and all energies appropriately. Comment on the overall favorability of the thermodynamics of the reaction you have illustrated. MM Kinetics E + S < == > E S < == > E + P (second step rate determining) This is basically it y axis of free energy Ea1 is DG # for step 1 and Ea2 is DG # for step 2 What is labeled DH here is DG. As shown this is a favorable reaction as DGrxn <0 3. In an assay for kinetics measurement for inhibition, okadaic acid (250 mm stock solution) was diluted. In each sample, 250 ul of the stock was and the final volume was adjusted to 3.0 ml. The experiment was conducted at room temperature. Assuming ideal behavior calculate: a) ΔH, ΔS and ΔG of dilution. With the assumption of ideality DH =0 DG = RT ln (C2/C1) C1= 250 mm C2 = 250mM*250uL/3000uL = mm DG = 8.314J/molK * 298* ln (20.83mM/250 mm) = J/mol = kj/mol DG = DH TDS J/mol = 0 298K (DS) DS = J/molK
4 b) What problems (if any) are inherent in the assumption made? Comment on the likelihood that the assumption is valid and explain why or why not. The assumption made is that the solution is ideal. This gives us DH=0. This solution is dilute so the solute solute interactions are minimal. However, there will be interactions between the solvent and solute. The more dilute the solution the more ideal the behavior so the diluted solution acts more ideally than the more concentrated solution (250mM). 4. In a regulator holding reservoir, gases from three 1 L tanks are being mixed to feed into a breathing tube. The gasses are N2, O2 and NO2, 14.0, 8.0 and 6.25g, respectively. The volume of the new tank is 2L and room temperature is maintained. Assuming the gases exhibit no reactivity or interactions with each other calculate the ΔH, ΔS and ΔG of mixing of the gases. Again DH = 0 (see problem 3) DGmixture = DG N2 + DG O2 + DGNO2 Concentrations 14.0g N2 = 0.5 mol; 8.0 g O2 = 0.25 mol and 6.25 g NO2 = mol Each initially in 1 L gives concentrations of 0.5, 0.25 and M, respectively Concentrations in the new tank are halved to 0.25, and M, respectively DG = RT ln (C2/C1) + RT ln (C2/C1) + RT ln (C2/C1) = RT (ln 0.25/0.5) + ln(0.125/0.25) + ln(0.0679/0.125) (or you can recognize that the dilution is ½ and occurring 3x) = 8.314J/molK (298K) *3ln J/mol Spontaneous (as expected for expansion of each gas into larger container) DS= 0 (- 5125J/mol)/298K = J/mol K (DS>0 for mixing) 5. What is the osmotic pressure created by a 1 M solution of glucose at human physiological temperature? What pressure would be generated by a 1M salt solution (NaCl). Explain the difference and compare your answer to the pressure you experience walking across campus (thermodynamic pressure not social or academic pressure!) pi = crt (C molar concentration) pi = 1mol/L ( Latm/molK)(310K) pi = atm (very large but this is a very concentrated solution at an elevated temperature!) for the salt since the dissolution results in two ions the effective concentration (assuming no ion pairing) is 2M and the pressure would be almost 51 atm!
5 In solid sugar, individual sugar molecules interact with each other by van der Waals forces. A salt is made up of anions and cations, and these interact electrostatically. Equimolar solutions of a salt and a sugar therefore do not have the same number of solute particles. Consequently, the osmotic pressure of the salt will ordinarily be greater than that of the sugar. Subtle solvent-interaction effects are important too, but the underlying cause of osmotic pressure is a soluble solute in a region of solution which can undergo expansion and which is separated from a region of higher concentration solvent by a semi-permeable membrane. 6. a) Calculate the osmotic pressure created by g of a 10kDa protein in 10 ml of dialysis tubing suspended in 200 ml water. The membrane cutoff is 1kDa. b) The tubing also contains 2.0g GdHCl salt used in unfolding the protein. What is the osmotic pressure created by the salt? c) At what concentration of salt will the system come to equilibrium (wrt salt)? d) Assuming the tubing can swell 3 fold what will be the pseudo equilibrium concentration of the protein? e)how much salt will remain in the swelled tubing at equilibrium? f) How much work will be done by the protein in tubing? a) pi = crt pi =(0.0015g / 10,000g/mol)/0.01L * Latm/molK * 298 K pi = atm (very small pressure because very few particles) b) pi = crt pi =(2.0g / 95.53g/mol)/0.01L * Latm/molK * 298 K pi = atm (much higher pressure more particles!) c) Equilibrium will occur when the concentration of salt throughout is constant. Total mass salt 2.0g with total volume (both sides of membrane) 210 ml (2.0g/95.53 g/mol)/0.210 L = = 0.10 M d) Equilibrium will occur when the concentration of protein throughout is constant. Initial concentration of protein: (0.0015g/10,000 g/mol)/0.010 L = 1.5E- 5 M Total mass protein g with total volume (both sides of membrane) 210 ml (0.0015g/10,000 g/mol)/0.210 L = 7.1E- 7 M (if protein could distribute throughout the entire solution) But the 10 kd protein cannot pass through the 1 kd cutoff membrane so water will move in. Since the tubing can swell 3 fold the final concentration of the protein (pseudo equilibrium) (0.0015g/10,000 g/mol)/0.03 L = 5E- 6 M pseudo equilibrium concentration
6 The initial GdHCl concentration inside membrane is 2.09 M. The true equilibrium concentration is 0.1 M. Salt can pass through the membrane so it will reach equilibrium. With a 30 ml membrane 0.1 mol/l * 0.03L * g/mol = 0.257g salt inside membrane at equilibrium e) assuming constant external pressure of atm w=- pdv = atm*(0.03L- 0.01L) * * J/Latm = J 7. Glutamine is an important biomolecule made from glutamate. Calculate the equilibrium constant for the reaction: Glutamate + NH3 <==> Glutamine + H2O a) Use standard free energies of formation data to obtain the free energy change for the reaction. DG = DGproducts DG reactants DG = (Glutamine + H2O) (Glutamate + NH3) DG o formation (kj/mol) Glutamate NH Glutamine H2O ( ) ( ) = 13.2 kj/mol (not spontaneous as written) b) Under physiological conditions, the concentration of ammonia is near 10 mm. Calculate the ratio of [glutamine]/[glutamate] at equilibrium. Assume the concentration of water is invariant. DG o = - RTlnKeq 13200J/mol = J/molK 298 K ln [glutamate][0.01m]/1[glutamine] = ln [glutamate][0.01m]/1[glutamine] e = [glutamate][0.01m]/1[glutamine] [glutamine] = [glutamate][0.01m] [glutamine]/[glutamate] = 2.04 c) Physiologically glutamine is synthesized by coupling with ATP hydrolysis Is this necessary or not - explain? Yes this is necessary as written the reaction is not spontaneous and will require an energetic driving force. d) Write the reaction for the coupled process. Glutamate + NH3 + ATP <==> Glutamine + H2O +ADP + Pi
7 e) Calculate the standard state free energy and the equilibrium constant for this reaction at STP. This can be done by using the value for part a of 13.2 kj/mol and adding the value for the ATP hydrolysis kj/mol overall kj/mol f) Assume NH3 and Pi are maintained at about 10mM and that the ration of ATP to ADP = 1. What is the ratio of glutamate to glutamine at equilibrium? DG o = - RTlnKeq J/mol= J/molK* 298 K*ln[glutamate][0.01M][ADP][Pi]/1[ATP][glutamine] 7.78 = ln [glutamate][0.01m] 2 /[glutamine] e 7.78 = [glutamate][0.01m] 2 /[glutamine] 2396 [glutamine] = [glutamate][0.01m] 2 [glutamine]/[glutamate] = 4.17E- 8 note large change with coupled reaction 8. ATP solutions are generally made fresh in the laboratory before use. If they are made ahead of time they must be stored at - 4 C. Explain haynie 5.5 Because ΔG < 0, ATP hydrolysis is spontaneous at room temperature. But ΔG = ΔH TΔS, so the driving force for hydrolysis is reduced by lowering the temperature, even if ΔH and ΔS are approximately constant in the temperature range of interest. Changes in ΔG are reflected in Keq, which as we have seen in Chapter 4 is the ratio of the rate of the forward reaction to the reverse reaction. The precise value of ΔG alone, however, does not tell us whether a reaction is fast or slow. The rate of the forward reaction of ATP hydrolysis depends on the correct orientation of a water molecule and the bond hydrolyzed. The rate of the reverse reaction depends on the diffusion of ADP and Pi, which must interact to produce ATP. At 4 C molecules move more slowly than at 25 C, slowing the rate of exploration of possible relative orientations of ATP and water and therefore reducing the rate of hydrolysis. The effect is much more pronounced at 20 C, because although there is still some movement of solvent, most of the water molecules are effectively fixed, because although there is still some movement of solvent, most of the water molecules are effectively fixed in a lattice and molecular reorientation is greatly reduced in comparison with the liquid state.
8 9. The synthesis of ATP under standard conditions requires 7.7 cal/mol. In vivo the synthesis is couplesd to the movement of 2 protons across a membrane. What ph difference exists across the mitochondrial membrane as a result of ATP synthesis? Haynie 5.37 The chemical equation describing the situation before us is: ATP + H20 + 2H + inside ADP + Pi + 2H + outside G = RTln([H + outside] 2 /[H + inside] 2 ) = RTln([H + outside]/[h + inside]) 2 = 2RT(2.303)log([H + outside]/[h + inside]) = 4.606RTlog([H + outside]/[h + inside]) = 4.606RT( ph). Solving for ph, ph = 7700 cal mol 1 /( cal mol 1 K K) = For the binding of a ligand to a protein at 25 o C and ph=7.0, K d = 1x10-7 M. What is the free energy change for association of the ligand with the protein under standard conditions? For the dissociation reaction, ΔG o' = RTlnK d ΔG o' = (8.315x10-3 kj/(molk))(298k)( 16.1) = kj/mol Dissociation is not favored under standard conditions. For the association reaction, ΔG o' = RTlnK a = RTln(1/K d ) ΔG o' = (8.314)(298)(16.1) = 39.9 kj/mol Association is favored under standard conditions.
reduction kj/mol
1. Glucose is oxidized to water and CO 2 as a result of glycolysis and the TCA cycle. The net heat of reaction for the oxidation is -2870 kj/mol. a) How much energy is required to produce glucose from
More informationPrinciples of Bioenergetics. Lehninger 3 rd ed. Chapter 14
1 Principles of Bioenergetics Lehninger 3 rd ed. Chapter 14 2 Metabolism A highly coordinated cellular activity aimed at achieving the following goals: Obtain chemical energy. Convert nutrient molecules
More informationChapter 19 Chemical Thermodynamics Entropy and free energy
Chapter 19 Chemical Thermodynamics Entropy and free energy Learning goals and key skills: Explain and apply the terms spontaneous process, reversible process, irreversible process, and isothermal process.
More informationb) What is the gradient at room temperature? Du = J/molK * 298 K * ln (1/1000) = kj/mol
Chem350 Practice Problems Membranes 1. a) What is the chemical potential generated by the movement of glucose by passive diffusion established by a 1000 fold concentration gradient at physiological temperature?
More informationChemical Thermodynamics. Chapter 18
Chemical Thermodynamics Chapter 18 Thermodynamics Spontaneous Processes Entropy and Second Law of Thermodynamics Entropy Changes Gibbs Free Energy Free Energy and Temperature Free Energy and Equilibrium
More informationLecture Series 9 Cellular Pathways That Harvest Chemical Energy
Lecture Series 9 Cellular Pathways That Harvest Chemical Energy Reading Assignments Review Chapter 3 Energy, Catalysis, & Biosynthesis Read Chapter 13 How Cells obtain Energy from Food Read Chapter 14
More information10/26/2010. An Example of a Polar Reaction: Addition of H 2 O to Ethylene. to Ethylene
6.5 An Example of a Polar Reaction: Addition of H 2 O to Ethylene Addition of water to ethylene Typical polar process Acid catalyzed addition reaction (Electophilic addition reaction) Polar Reaction All
More informationLecture 3: Thermodynamics
3 LAWS OF THERMODYNAMICS Lecture 3: Thermodynamics Matter and energy are conserved Margaret A. Daugherty Fall 2004 Entropy always increases Absolute zero is unattainable System and Surroundings 1st Law
More informationOther Cells. Hormones. Viruses. Toxins. Cell. Bacteria
Other Cells Hormones Viruses Toxins Cell Bacteria ΔH < 0 reaction is exothermic, tells us nothing about the spontaneity of the reaction Δ H > 0 reaction is endothermic, tells us nothing about the spontaneity
More informationLecture 20. Chemical Potential
Lecture 20 Chemical Potential Reading: Lecture 20, today: Chapter 10, sections A and B Lecture 21, Wednesday: Chapter 10: 10 17 end 3/21/16 1 Pop Question 7 Boltzmann Distribution Two systems with lowest
More information= (-22) = +2kJ /mol
Lecture 8: Thermodynamics & Protein Stability Assigned reading in Campbell: Chapter 4.4-4.6 Key Terms: DG = -RT lnk eq = DH - TDS Transition Curve, Melting Curve, Tm DH calculation DS calculation van der
More informationEnergy and Cells. Appendix 1. The two primary energy transformations in plants are photosynthesis and respiration.
Energy and Cells Appendix 1 Energy transformations play a key role in all physical and chemical processes that occur in plants. Energy by itself is insufficient to drive plant growth and development. Enzymes
More informationThe energy of oxidation of 11 g glucose = kj = kg/m 2 s 2
Chem 350 thermo problems Key 1. How many meters of stairway could a 70kg man climb if all the energy available in metabolizing an 11 g spoonful of sugar to carbon dioxide and water could be converted to
More informationApplications of Free Energy. NC State University
Chemistry 433 Lecture 15 Applications of Free Energy NC State University Thermodynamics of glycolysis Reaction kj/mol D-glucose + ATP D-glucose-6-phosphate + ADP ΔG o = -16.7 D-glucose-6-phosphate p D-fructose-6-phosphate
More informationf) Adding an enzyme does not change the Gibbs free energy. It only increases the rate of the reaction by lowering the activation energy.
Problem Set 2-Answer Key BILD1 SP16 1) How does an enzyme catalyze a chemical reaction? Define the terms and substrate and active site. An enzyme lowers the energy of activation so the reaction proceeds
More informationThe Laws of Thermodynamics
Entropy I. This, like enthalpy, Thus, II. A reaction is ( more on this later) if: (H, enthalpy) (S, entropy) III. IV. Why does entropy happen? Probability It s harder to keep things in order (look at my
More informationChapter 17.3 Entropy and Spontaneity Objectives Define entropy and examine its statistical nature Predict the sign of entropy changes for phase
Chapter 17.3 Entropy and Spontaneity Objectives Define entropy and examine its statistical nature Predict the sign of entropy changes for phase changes Apply the second law of thermodynamics to chemical
More informationFree Energy. because H is negative doesn't mean that G will be negative and just because S is positive doesn't mean that G will be negative.
Biochemistry 462a Bioenergetics Reading - Lehninger Principles, Chapter 14, pp. 485-512 Practice problems - Chapter 14: 2-8, 10, 12, 13; Physical Chemistry extra problems, free energy problems Free Energy
More informationLecture 2: Biological Thermodynamics [PDF] Key Concepts
Lecture 2: Biological Thermodynamics [PDF] Reading: Berg, Tymoczko & Stryer: pp. 11-14; pp. 208-210 problems in textbook: chapter 1, pp. 23-24, #4; and thermodynamics practice problems [PDF] Updated on:
More informationDepartment of Chemistry and Biochemistry University of Lethbridge. Biochemistry II. Bioenergetics
Department of Chemistry and Biochemistry University of Lethbridge II. Bioenergetics Slide 1 Bioenergetics Bioenergetics is the quantitative study of energy relationships and energy conversion in biological
More informationEquations: q trans = 2 mkt h 2. , Q = q N, Q = qn N! , < P > = kt P = , C v = < E > V 2. e 1 e h /kt vib = h k = h k, rot = h2.
Constants: R = 8.314 J mol -1 K -1 = 0.08206 L atm mol -1 K -1 k B = 0.697 cm -1 /K = 1.38 x 10-23 J/K 1 a.m.u. = 1.672 x 10-27 kg 1 atm = 1.0133 x 10 5 Nm -2 = 760 Torr h = 6.626 x 10-34 Js For H 2 O
More information7/19/2011. Models of Solution. State of Equilibrium. State of Equilibrium Chemical Reaction
Models of Solution Chemistry- I State of Equilibrium A covered cup of coffee will not be colder than or warmer than the room temperature Heat is defined as a form of energy that flows from a high temperature
More informationChemistry 123: Physical and Organic Chemistry Topic 2: Thermochemistry S H 2 = S H 2 R ln P H2 P NH
N (g) + 3 H (g) NH 3 (g) S N = S H = S NH 3 = S N R ln P N S H R ln P H S NH 3 R ln P NH3 ΔS rxn = (S Rln P NH 3 NH3 ) (S N Rln P N ) 3 (S H Rln P H ) ΔS rxn = S S NH 3 N 3S H + Rln P P 3 N H ΔS rxn =
More informationBasic Concepts of Metabolism. Stages of Catabolism. Key intermediates 10/12/2015. Chapter 15, Stryer Short Course
Basic Concepts of Metabolism Chapter 15, Stryer Short Course Digestion Formation of key intermediate small molecules Formation of ATP Stages of Catabolism Key intermediates 1 Fundamental Needs for Energy
More informationDisorder and Entropy. Disorder and Entropy
Disorder and Entropy Suppose I have 10 particles that can be in one of two states either the blue state or the red state. How many different ways can we arrange those particles among the states? All particles
More informationChpt 19: Chemical. Thermodynamics. Thermodynamics
CEM 152 1 Reaction Spontaneity Can we learn anything about the probability of a reaction occurring based on reaction enthaplies? in general, a large, negative reaction enthalpy is indicative of a spontaneous
More informationChapter 6. Ground Rules Of Metabolism
Chapter 6 Ground Rules Of Metabolism Alcohol Dehydrogenase An enzyme Breaks down ethanol and other toxic alcohols Allows humans to drink Metabolism Is the totality of an organism s chemical reactions Arises
More informationCHEM N-2 November 2014
CHEM1612 2014-N-2 November 2014 Explain the following terms or concepts. Le Châtelier s principle 1 Used to predict the effect of a change in the conditions on a reaction at equilibrium, this principle
More informationChem1B General Chemistry II Exam 1 Summer Read all questions carefully make sure that you answer the question that is being asked.
ChemB General Chemistry II Exam Summer 20 Name: KEY GSI: Write your name on all pages of the exam. Read all questions carefully make sure that you answer the question that is being asked. Write neatly
More informationGibbs Free Energy. Evaluating spontaneity
Gibbs Free Energy Evaluating spontaneity Predicting Spontaneity An increase in entropy; Changing from a more structured to less structured physical state: Solid to liquid Liquid to gas Increase in temperature
More informationChem 350 Problem Set 1 Thermodynamics Key
Chem 350 Problem Set 1 Thermodynamics 2018 - Key 1. A man at sea level with a 1.0 L resting lung capacity breathes deeply inhaling one mole of gas increasing his lung capacity to 1.6 L. Temperature remains
More informationEntropy, Free Energy, and Equilibrium
Entropy, Free Energy, and Equilibrium Chapter 17 Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 1 Spontaneous Physical and Chemical Processes A waterfall runs
More information12A Entropy. Entropy change ( S) N Goalby chemrevise.org 1. System and Surroundings
12A Entropy Entropy change ( S) A SPONTANEOUS PROCESS (e.g. diffusion) will proceed on its own without any external influence. A problem with H A reaction that is exothermic will result in products that
More informationChem Lecture 4 Enzymes Part 1
Chem 452 - Lecture 4 Enzymes Part 1 Question of the Day: Enzymes are biological catalysts. Based on your general understanding of catalysts, what does this statement imply about enzymes? Introduction Enzymes
More informationChapter 6- An Introduction to Metabolism*
Chapter 6- An Introduction to Metabolism* *Lecture notes are to be used as a study guide only and do not represent the comprehensive information you will need to know for the exams. The Energy of Life
More informationCh 17 Free Energy and Thermodynamics - Spontaneity of Reaction
Ch 17 Free Energy and Thermodynamics - Spontaneity of Reaction Modified by Dr. Cheng-Yu Lai spontaneous nonspontaneous Spontaneous Processes Processes that are spontaneous in one direction are nonspontaneous
More informationChemistry 1A, Spring 2007 Midterm Exam 3 April 9, 2007 (90 min, closed book)
Chemistry 1A, Spring 2007 Midterm Exam 3 April 9, 2007 (90 min, closed book) Name: KEY SID: TA Name: 1.) Write your name on every page of this exam. 2.) This exam has 34 multiple choice questions. Fill
More informationLS1a Fall 2014 Practice Problem Set #1. 1. Consider a hypothetical reaction carried out at constant temperature and pressure:
LS1a Fall 2014 Practice Problem Set #1 I. Basic Concept Questions 1. Consider a hypothetical reaction carried out at constant temperature and pressure: The Gibbs free energy curve of this reaction is depicted
More informationReaction Thermodynamics
Reaction Thermodynamics Thermodynamics reflects the degree to which a reaction is favored or disfavored Recall: G = Gibbs free energy = the energy available to do work ΔG = change in G of the system as
More informationEnergy, Enzymes, and Metabolism. Energy, Enzymes, and Metabolism. A. Energy and Energy Conversions. A. Energy and Energy Conversions
Energy, Enzymes, and Metabolism Lecture Series 6 Energy, Enzymes, and Metabolism B. ATP: Transferring Energy in Cells D. Molecular Structure Determines Enzyme Fxn Energy is the capacity to do work (cause
More informationHomework Problem Set 8 Solutions
Chemistry 360 Dr. Jean M. Standard Homework roblem Set 8 Solutions. Starting from G = H S, derive the fundamental equation for G. o begin, we take the differential of G, dg = dh d( S) = dh ds Sd. Next,
More information*The entropy of a system may decrease, but the entropy of the system plus its surroundings must always increase
AP biology Notes: Metabolism Metabolism = totality of an organism's chemical process concerned with managing cellular resources. Metabolic reactions are organized into pathways that are orderly series
More informationBIOCHEMISTRY. František Vácha. JKU, Linz.
BIOCHEMISTRY František Vácha http://www.prf.jcu.cz/~vacha/ JKU, Linz Recommended reading: D.L. Nelson, M.M. Cox Lehninger Principles of Biochemistry D.J. Voet, J.G. Voet, C.W. Pratt Principles of Biochemistry
More informationCHEM Exam 3 - March 31, 2017
CHEM 3530 - Exam 3 - March 31, 2017 Constants and Conversion Factors NA = 6.02x10 23 mol -1 R = 8.31 J/mol-K = 8.31 kpa-l/mol-k 1 bar = 100 kpa = 750 torr 1 kpa = 7.50 torr 1 J = 1 kpa-l 1 kcal = 4.18
More informationChemistry 5.07SC Biological Chemistry I Fall Semester, 2013
Chemistry 5.07SC Biological Chemistry I Fall Semester, 2013 Lecture 10. Biochemical Transformations II. Phosphoryl transfer and the kinetics and thermodynamics of energy currency in the cell: ATP and GTP.
More informationBiological Thermodynamics
Biological Thermodynamics Classical thermodynamics is the only physical theory of universal content concerning which I am convinced that, within the framework of applicability of its basic contents, will
More informationSparks CH301 GIBBS FREE ENERGY. UNIT 4 Day 8
Sparks CH301 GIBBS FREE ENERGY UNIT 4 Day 8 What are we going to learn today? Quantify change in Gibbs Free Energy Predict Spontaneity at Specific Temperatures QUIZ: iclicker Questions S H2 = 131 J/K mol
More informationChapter 5. Simple Mixtures Fall Semester Physical Chemistry 1 (CHM2201)
Chapter 5. Simple Mixtures 2011 Fall Semester Physical Chemistry 1 (CHM2201) Contents The thermodynamic description of mixtures 5.1 Partial molar quantities 5.2 The thermodynamic of Mixing 5.3 The chemical
More informationAn Introduction to Metabolism
Chapter 8 An Introduction to Metabolism oweroint Lectures for Biology, Seventh Edition Neil Campbell and Jane Reece Concept 8.1: An organism s metabolism transforms matter and energy, subject to the laws
More informationThe underlying prerequisite to the application of thermodynamic principles to natural systems is that the system under consideration should be at equilibrium. http://eps.mcgill.ca/~courses/c220/ Reversible
More information4/19/2016. Chapter 17 Free Energy and Thermodynamics. First Law of Thermodynamics. First Law of Thermodynamics. The Energy Tax.
Chemistry: A Molecular Approach, 2nd Ed. Nivaldo Tro First Law of Thermodynamics Chapter 17 Free Energy and Thermodynamics You can t win! First Law of Thermodynamics: Energy cannot be created or destroyed
More informationName AP CHEM / / Collected AP Exam Essay Answers for Chapter 16
Name AP CHEM / / Collected AP Exam Essay Answers for Chapter 16 1980 - #7 (a) State the physical significance of entropy. Entropy (S) is a measure of randomness or disorder in a system. (b) From each of
More informationChemical standard state: 1 M solutes, pure liquids, 1 atm gases Biochemical standard state: ph 7, all species in the ionic form found at ph 7
Chemistry 271, Section 22xx Your Name: Prof. Jason Kahn University of Maryland, College Park Your SID #: General Chemistry and Energetics Exam II (100 points total) Your Section #: November 4, 2009 You
More informationThermodynamics is the study of energy and its effects on matter
00Note Set 3 1 THE ENERGETICS OF LIFE Thermodynamics and Bioenergetics: Thermodynamics is the study of energy and its effects on matter Bioenergetics is the quantitative analysis of how organisms gain
More informationThermodynamics. Thermodynamically favored reactions ( spontaneous ) Enthalpy Entropy Free energy
Thermodynamics Thermodynamically favored reactions ( spontaneous ) Enthalpy Entropy Free energy 1 Thermodynamically Favored Processes Water flows downhill. Sugar dissolves in coffee. Heat flows from hot
More informationFull file at https://fratstock.eu
Chapter 03 1. a. DG=DH-TDS Δ G = 80 kj ( 98 K) 0.790 kj = 44.6 kj K b. ΔG = 0 @ T m. Unfolding will be favorable at temperatures above the T m. Δ G =Δ H TΔ S 0 kj kj 80 ( xk) 0.790 K 0 Δ G = = 354.4 K
More informationSample Question Solutions for the Chemistry of Life Topic Test
Sample Question Solutions for the Chemistry of Life Topic Test 1. Enzymes play a crucial role in biology by serving as biological catalysts, increasing the rates of biochemical reactions by decreasing
More informationChapter 8: An Introduction to Metabolism. 1. Energy & Chemical Reactions 2. ATP 3. Enzymes & Metabolic Pathways
Chapter 8: An Introduction to Metabolism 1. Energy & Chemical Reactions 2. ATP 3. Enzymes & Metabolic Pathways 1. Energy & Chemical Reactions 2 Basic Forms of Energy Kinetic Energy (KE) energy in motion
More information= 16! = 16! W A = 3 = 3 N = = W B 3!3!10! = ΔS = nrln V. = ln ( 3 ) V 1 = 27.4 J.
Answer key: Q1A Both configurations are equally likely because the particles are non-interacting (i.e., the energy does not favor one configuration over another). For A M = 16 N = 6 W A = 16! 0.9 101 =
More informationChapter 8: An Introduction to Metabolism
Chapter 8: An Introduction to Metabolism Key Concepts 8.1 An organism s metabolism transforms matter and energy, subject to the laws of thermodynamics 8.2 The free-energy change of a reaction tells us
More informationEntropy, Free Energy and the Direction of Chemical Reactions
Thermodynamics: Entropy, Free Energy and the Direction of Chemical Reactions Dr.ssa Rossana Galassi 320 4381420 rossana.galassi@unicam.it 20-1 Thermodynamics: Entropy, Free Energy, and the Direction of
More informationChapter 19. Chemical Thermodynamics. Chemical Thermodynamics
Chapter 19 Enthalpy A thermodynamic quantity that equal to the internal energy of a system plus the product of its volume and pressure exerted on it by its surroundings; Enthalpy is the amount of energy
More informationChapter 7 Chemical Reactions: Energy, Rates, and Equilibrium
Chapter 7 Chemical Reactions: Energy, Rates, and Equilibrium Introduction This chapter considers three factors: a) Thermodynamics (Energies of Reactions) a reaction will occur b) Kinetics (Rates of Reactions)
More informationThermodynamics. Chem 36 Spring The study of energy changes which accompany physical and chemical processes
Thermodynamics Chem 36 Spring 2002 Thermodynamics The study of energy changes which accompany physical and chemical processes Why do we care? -will a reaction proceed spontaneously? -if so, to what extent?
More information7. a. A spontaneous process is one that occurs without any outside intervention.
CHAPTER SIXTEEN SPONTANEITY, ENTROPY, AND FREE ENERGY Questions 7. a. A spontaneous process is one that occurs without any outside intervention. b. Entropy is a measure of disorder or randomness. c. The
More informationBIOC : Homework 1 Due 10/10
Contact information: Name: Student # BIOC530 2012: Homework 1 Due 10/10 Department Email address The following problems are based on David Baker s lectures of forces and protein folding. When numerical
More informationMetabolism and enzymes
Metabolism and enzymes 4-11-16 What is a chemical reaction? A chemical reaction is a process that forms or breaks the chemical bonds that hold atoms together Chemical reactions convert one set of chemical
More informationChapter 3: Energy and Work. Energy and Work, con t. BCH 4053 Spring 2003 Chapter 3 Lecture Notes. Slide 1. Slide 2
BCH 4053 Spring 2003 Chapter 3 Lecture Notes 1 Chapter 3: Thermodynamics of Biological Systems 2 Energy and Work Work = force x distance Energy = ability to do work Mechanical Energy Kinetic Energy = mv
More informationSolution W2009 NYB Final exam
Solution W009 NYB Final exam Question Consider one liter of solution with [H SO 4 3.75 mol/l. Then : Mass of solution: 000 ml x.3 g/ml 30 g solution mass of H SO 4 : 3.75 mol /L x 98.078 g/mol 368 g mass
More informationChemistry and the material world Unit 4, Lecture 4 Matthias Lein
Chemistry and the material world 123.102 Unit 4, Lecture 4 Matthias Lein Gibbs ree energy Gibbs ree energy to predict the direction o a chemical process. Exergonic and endergonic reactions. Temperature
More informationExp.3 Determination of the Thermodynamic functions for the Borax Solution
Exp.3 Determination of the Thermodynamic functions for the Borax Solution Theory: The relationship between Gibb s energy (ΔG), Enthalpy (ΔH), Entropy (ΔS) and the equilibrium constant (K) for a chemical
More informationCHM 152 Final Exam Review
CHM 152 Final Exam Review Kinetics Chapter 12 End-of-Chapter Suggested problems: 1, 2, 3, 4, 6, 7, 9, 11, 13, 14, 15, 17, 19, 21, 25, 29, 31, 33 (graphing), 37, 39, 41, 47, 51, 53, 57, 63, 67, 68, 69,
More informationEntropy. 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
Entropy Spontaneity process a process that occurs without intervention can be fast or slow Entropy (s) the measure of molecular randomness or disorder Think of entropy as the amount of chaos Entropy Predict
More informationLecture 27. Transition States and Enzyme Catalysis
Lecture 27 Transition States and Enzyme Catalysis Reading for Today: Chapter 15 sections B and C Chapter 16 next two lectures 4/8/16 1 Pop Question 9 Binding data for your thesis protein (YTP), binding
More informationBIOLOGICAL SCIENCE. Lecture Presentation by Cindy S. Malone, PhD, California State University Northridge. FIFTH EDITION Freeman Quillin Allison
BIOLOGICAL SCIENCE FIFTH EDITION Freeman Quillin Allison 8 Lecture Presentation by Cindy S. Malone, PhD, California State University Northridge Roadmap 8 In this chapter you will learn how Enzymes use
More informationCHEMISTRY - CLUTCH CH CHEMICAL THERMODYNAMICS.
!! www.clutchprep.com CONCEPT: THERMOCHEMICAL PROCESSES is the branch of physical science concerned with heat and its transformations to and from other forms of energy. In terms of a chemical reaction,
More informationmol mol b) The movement of positive ions into the mito produces a free energy change of 7 in 6 out
Chapter 5 Problems Page 1 of 5 11/1/27 5.5 Chemiosmotic theory says that a mitochondrial proton gradient powers ATP synthesis. The mitochondrial membrane potential is -14 mv and ΔpH 1.5. Inside the mitochondrion
More informationconcentrations (molarity) rate constant, (k), depends on size, speed, kind of molecule, temperature, etc.
#80 Notes Ch. 12, 13, 16, 17 Rates, Equilibriums, Energies Ch. 12 I. Reaction Rates NO 2(g) + CO (g) NO (g) + CO 2(g) Rate is defined in terms of the rate of disappearance of one of the reactants, but
More informationAn Introduction to Metabolism
Chapter 8 An Introduction to Metabolism Dr. Wendy Sera Houston Community College Biology 1406 Key Concepts in Chapter 8 1. An organism s metabolism transforms matter and energy, subject to the laws of
More informationPathways that Harvest and Store Chemical Energy
6 Pathways that Harvest and Store Chemical Energy Energy is stored in chemical bonds and can be released and transformed by metabolic pathways. Chemical energy available to do work is termed free energy
More informationChemistry 102 Spring 2016 Discussion #12, Chapter 17 Student name TA name Section. Things you should know when you leave Discussion today: ( G o f
Chemistry 10 Spring 016 Discussion #1, Chapter 17 Student name TA name Section Things you should know when you leave Discussion today: 1. ΔS sys = Δ r S = Σ [n i (S )] product - Σ [n j (S )] reactants.
More informationChem/Biochem 471 Exam 2 11/14/07 Page 1 of 7 Name:
Page 1 of 7 Please leave the exam pages stapled together. The formulas are on a separate sheet. This exam has 5 questions. You must answer at least 4 of the questions. You may answer all 5 questions if
More informationMetabolism and Enzymes
Energy Basics Metabolism and Enzymes Chapter 5 Pgs. 77 86 Chapter 8 Pgs. 142 162 Energy is the capacity to cause change, and is required to do work. Very difficult to define quantity. Two types of energy:
More informationII. The Significance of the Signs Property Positive (+) Negative (-)
Entropy I. Entropy, S, is the measure of the disorder of a system. A. This, like enthalpy, cannot be measured. B. Thus, only the change in disorder ( S) can be measured. II. A reaction is spontaneous (more
More informationPresentation Microcalorimetry for Life Science Research
Presentation Microcalorimetry for Life Science Research MicroCalorimetry The Universal Detector Heat is either generated or absorbed in every chemical process Capable of thermal measurements over a wide
More informationUnit 5: Spontaneity of Reaction. You need to bring your textbooks everyday of this unit.
Unit 5: Spontaneity of Reaction You need to bring your textbooks everyday of this unit. THE LAWS OF THERMODYNAMICS 1 st Law of Thermodynamics Energy is conserved ΔE = q + w 2 nd Law of Thermodynamics A
More informationSCORING. The exam consists of 5 questions totaling 100 points as broken down in this table:
UNIVERSITY OF CALIFORNIA, BERKELEY CHEM C130/MCB C100A MIDTERM EXAMINATION #2 OCTOBER 20, 2016 INSTRUCTORS: John Kuriyan and David Savage THE TIME LIMIT FOR THIS EXAMINATION: 1 HOUR 50 MINUTES SIGNATURE:
More informationActivity: Identifying forms of energy
Activity: Identifying forms of energy INTRODUCTION TO METABOLISM Metabolism Metabolism is the sum of all chemical reactions in an organism Metabolic pathway begins with a specific molecule and ends with
More informationJudith Herzfeld 1997,1999. These exercises are provided here for classroom and study use only. All other uses are copyright protected.
Judith Herzfeld 1997,1999 These exercises are provided here for classroom and study use only. All other uses are copyright protected. 5.5-010 Which of the following statements is not valid concerning a
More informationSpontaneity, Entropy, and Free Energy
Spontaneity, Entropy, and Free Energy A ball rolls spontaneously down a hill but not up. Spontaneous Processes A reaction that will occur without outside intervention; product favored Most reactants are
More informationAccelerated Chemistry Semester 2 Review Sheet
Accelerated Chemistry Semester 2 Review Sheet The semester test will be given in two parts. The first part is a performance assessment and will be given the day before the semester test. This will include
More informationMCB100A/Chem130 MidTerm Exam 2 April 4, 2013
MCBA/Chem Miderm Exam 2 April 4, 2 Name Student ID rue/false (2 points each).. he Boltzmann constant, k b sets the energy scale for observing energy microstates 2. Atoms with favorable electronic configurations
More informationChapter 15 part 2. Biochemistry I Introduction to Metabolism Bioenergetics: Thermodynamics in Biochemistry. ATP 4- + H 2 O ADP 3- + P i + H +
Biochemistry I Introduction to Metabolism Bioenergetics: Thermodynamics in Biochemistry ATP 4- + 2 ADP 3- + P i 2- + + Chapter 15 part 2 Dr. Ray 1 Energy flow in biological systems: Energy Transformations
More information2017 Ebneshahidi. Dr. Ali Ebneshahidi
Dr. Ali Ebneshahidi A. Introduction Chemistry science that deals with the composition of substances and the changes that take place in their composition. Organic chemistry chemistry that deals with organic
More information9/25/2011. Outline. Overview: The Energy of Life. I. Forms of Energy II. Laws of Thermodynamics III. Energy and metabolism IV. ATP V.
Chapter 8 Introduction to Metabolism Outline I. Forms of Energy II. Laws of Thermodynamics III. Energy and metabolism IV. ATP V. Enzymes Overview: The Energy of Life Figure 8.1 The living cell is a miniature
More informationThermodynamics and Kinetics
Thermodynamics and Kinetics Lecture 12 Free Energy Applications NC State University Isolated system requires DS > 0 DS sys > 0 Isolated system: Entropy increases for any spontaneous process System and
More informationChapter 8 Notes. An Introduction to Metabolism
Chapter 8 Notes An Introduction to Metabolism Describe how allosteric regulators may inhibit or stimulate the activity of an enzyme. Objectives Distinguish between the following pairs of terms: catabolic
More informationEnergy Transformation and Metabolism (Outline)
Energy Transformation and Metabolism (Outline) - Definitions & Laws of Thermodynamics - Overview of energy flow ecosystem - Biochemical processes: Anabolic/endergonic & Catabolic/exergonic - Chemical reactions
More informationThe altercation described above is responsible for the formation of what critical biological structure?
LAUGH to release tension and get points!!!! Extra Bonus +2 The altercation described above is responsible for the formation of what critical biological structure? This hydrophobic interaction is the basis
More informationEnergy is the capacity to do work
1 of 10 After completing this chapter, you should, at a minimum, be able to do the following. This information can be found in my lecture notes for this and other chapters and also in your text. Correctly
More information