Thermodynamics (XI) Assignment(Solution)

Size: px
Start display at page:

Download "Thermodynamics (XI) Assignment(Solution)"

Transcription

1 SYLLABUS CUM COM./XI/03 4 hermodynamics (XI) Assignment(Solution) Comprehension ype Questions aragraph for Question -5 For an ideal gas, an illustration of three different paths A, (B + C) and (D + E) from an initial state,, to a final state,, is shown in the given figure. ath A represents a reversible isothermal expansion from, to,. ath (B + C) represents a reversible adiabatic expansion (B) from, to 3,, followed by reversible heating the gas at constant volume (C) from 3,, to,,. ath (D + E) represents a reversible expansion at constant pressure (D) from,, to,, 3 followed by a reversible cooling at constant volume (E) from,, 3 to,,. Q. What is q rev, for path (A)? (a) ( ) (b) nr ln (c) nr ln (d) nr ln (d) According to the first law of thermodynamics U = q w In isothermal process, U = 0 q = w or w = nr ln Q. What is q rev, for path (B + C)? (a) nr ln (b) nr ln (c) zero (d) nr ln ath (B + C) occurs in adiabatic conditions q = 0 We know that q S = rev q rev = S q rev = nr ln Q3. What is S for path A? (a) nr ln (b) ( ) (c) ( ) (d) nr( ) (a) For path A qrev nr S = ln nr ln Q4. What is q rev, for path (D + E)? (a) ( ) (b) Cv () d (c) nr ln (d) 3 C () d (a) w = q = ( ) 3 S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Broaden Your Horizon []

2 SYLLABUS CUM COM./XI/03 4 Q5. What is S for path (D + E)? (a) ( ) (b) nr ln (d) For path (D + E) S = nrln (c) + ( ) (d) nr ln aragraph for Question 6-0 A sample of ideal gas undergoes isothermal expansion in a reversible manner from volume to volume. he initial pressure is and the final pressure is. he same sample is then allowed to undergo reversible expansion under adiabatic conditions from volume to. he initial pressure being same but final pressure is. Q6. he work of expansion in adiabatic process (w adi ) is related to work of expansion in isothermal process (w iso ) as (a) w adi = w iso (b) w adi < w iso (c) w adi = w iso (d) w adi > w iso (b) Work in reversible isothermal expansion is greater than work done in adiabatic expansion. Q7. Which of the following is correct? (a) = (b) / = / (c) / = / 3 (d) = (a) = (Boyle s law) Q8. Which graphic representation is correct (b) Q9. If 3 and are equal, then (a) (adi) = (iso) (b) (adia) < (iso) (c) Both (adi) = (iso) < (d) (adi) > (iso) (d) Cp Q0. Which relation is correct? C (a) = 3 (b) = 3 (c) = (d) (c) aragraph for Question -5 he state of a mole of an ideal gas changed from state A at pressure and volume follows four different processes and finally returns to initial state A reversibly as shown below in the graph. By interpreting the graph, answer the following questions. Q. Which is the kind of process followed from state A to state B? (a) Isochoric expansion (b) Isobaric expansion (c) Isothermal reversible expansion (d) Isothermal irreversible compression (b) Expansion from state A to state B occurs at constant pressure (isobaric expansion) = S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Broaden Your Horizon []

3 SYLLABUS CUM COM./XI/03 4 Q. In state D to state A, what kind of process is followed? (a) Isobaric expansion (b) Isobaric compression (c) Isochoric process (d) Isothermal compression (c) Expansion from state D to state A occurs at constant volume (isochoric process)= Q3. What would the be total work done by the gas? (a) (b) (c) 0 (d) Zero (a) Work done = - Or -( ) = - Q4. What would be the work done in state B to C? (a) (b) (c) (d) Zero (d) In conversion from B to C, volume does not change or = 0, therefore w = 0. Q5. What would be the heat absorbed by the system in this cyclic process? (a) - (b) Zero (c) (d) (d) q = - w q = aragraph for Question A sample consisting of mol of a mono-atomic perfect gas C R is taken through the cycle as shown. Q6. emperature at points (), (), and (3), respectively is (a) 73 K, 546K, 73 K (b) 546 K, 73 K, 73 K (c) 73 K, 73 K, 73 K (d) 546 K, 546 K, 73 K (a) Q7. H for the overall cycle is (a) J (b) J (c) J (d) Zero (d) In cyclic process, H = 0. Q8. U for the process ( ) is (a) 0.00 J (b) kj (c) J (d) J (b) In expansion from state to state. = atm =.44 L = L C = 3 R = = = 73 K U = nc = = J Q9. U for the process ( 3) is (a) 0.00 J (b) kj (c) kj (d) None of these (c) In conversion from state to state 3 = = = - 73 K C = 3 R U = nc = (-73) = J S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Broaden Your Horizon [3]

4 SYLLABUS CUM COM./XI/03 4 aragraph for Question 0-4 he pressure volume of varius thermodynamics processes is shown in graphs: Work is the mode of transference of energy. It has been observed that reversible work done by the system is the maximum obtainable work. w rev > w irr he works of isothermal and adiabatic processes are different from each other. w isothermal reversible =.303nRlog 0 =.303nR log 0 w adiabatic reversible = C v ( - ) Q0. If w, w, w 3, and w 4 are work done in isothermal, adiabatic, isobaric, and isochoric reversible processes, respectively then the correct sequence (for expansion) would be (a) w < w < w 3 < w 4 (b) w 3 = w = w = w 4 (c) w 3 < w < w 4 < w (d) w 3 > w > w > w 4 (d) w = Work done = Area under curve Q. A thermodynamic system goes in a cyclic process as represented in the following - diagram: he network done during the complete cycle is given by the area (a) Cycle ACBDA (b) AA B BDA (c) AA B B (d) Area not bonded by curve (a) Q. - plots for two gases during adiabatic processes are given in the given figure.: lot D and lot C should correspond to (a) He and O (b) He and Ar (c) O and He (d) O and N (c) Slopw of the adiabatic curve Slope of B > slope of A He ( =.66); O ( =.44) S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Broaden Your Horizon [4]

5 SYLLABUS CUM COM./XI/03 4 Q3. he q value and work done in isothermal reversible expansion of one mole of an ideal gas from initial pressure of bar to final pressure of 0. bar at constant temperature 73 K are: (a) 5. kj, -5. kj (b) +6. kj, 6. kj (c) 5. J, 5. J (d) -6. J, -6. J (a) w = nrlog = log = -5.7 kj 0. q = - w = kj for isothermal process Q4. Calculate work done when mole of an ideal gas is expanded reversibly from 30 L to 60 L at a constant temperature of 300 K (a) 8.78 kj (b) -.73 kj (c) 0.73 kj (d) kj (b) Matching ype Questions Q5. Match the following (a) Joule-homson coefficient (p) U 0 (b) Kirchhoff s equation (q) a b 0 R (c) Ideal gas (r) H C (d) Inversion temperature (s) ( H/ ) H C (a s) (b r) Kirchoff s equation relate the variation of enthalpy with temperature. U (c p) For ideal gas, 0 a (d q) Inversion temperature, i = Rb Q6. Match the following hermodynamic properties Relation (a) G (p) -R log K (b) H Θ (q) ln K R (c) S Θ (r) -nfe (d) G Θ (s) G - (a p, r) (b q) (c s) (d p, r) Multiple Correct Answer ype Questions Q7. Which is not correct relationship? dh du du (a) d d = (+ve) (b) d = 0 (for ideal gas) d nr (c) d = (for ideal gas) (d) All of these H U (a, c) R Q8. Which of the following are not correct at 98 K? (a) f G Θ element = 0 (b) f H Θ element = 0 (c) f S Θ element = 0 (d) f G Θ compound = 0 (b, c, d) S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Broaden Your Horizon [5]

6 SYLLABUS CUM COM./XI/03 4 S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Single Correct Answer ype Questions Q9. For the reaction; X O 4 (l) XO (g) U =. kcal, S = 0 cal K - at 300 K Hence G is (a).7 kcal (b) -.7 kcal (c) 9.3 kcal (d) -9.3 kcal (b) H = U + n g R = = 3.3 kcal G = H - S = (0.0) = -.7 kcal Q30. If G = H S and G = H + temperature, is given by: H G (a) (b) nf nf (c) On comparison: d( G) S = - d d( G) d S (c) nf then variation of EMF of a cell E, with (d) S nf d( nfe) de HereEis the S = - nf d d Emf of cell de S d nf Q3. mol of NH 3 gas at 7C is expanded under adiabatic condition to make volume 8 times ( =.33). Final temperature and work done, respectively, are (a) 50 K, 900 cal (b) 50 K, 400 cal (c) 50 K, 000 cal (d) 00 K, 800 cal (a) = = 50 K w = -C = -C ( - ) = - 3 (50-300) = 900 kcal Q3. he standard heat of combustion of Al is kj mol - at 5C. If Al reacts with O at 5C, which of the following release 50 kj of heat? (a) he reaction of 0.64 mol of Al (b) he formation of 0.64 mol of Al O 3 (c) he reaction of 0.3 mol of Al (d) he formation of 0.50 mol of Al O 3 (d) Al + 3 O Al O 3 7g H = kj mol - (a) 0.64 mol of Al = on combustion gave = 53 kj. Hence false. (b) Formation of 0.64 mol of Al O 3 gave = = 045 kj Hence, false. (c) 0.3 mol of Al on combustion gave = 6 kj. Hence false (d) Formation of 0.50 mol of Al O 3 give = 5.3 kj Hence, true. Q33. Inversion temperature is Rb a Rb a (a) (b) (c) (d) a Rb a Rb (b) Q34. For an ideal gas Joule-homson coefficient is: (a) ositive (b) Negative (c) Zero (d) Dependent on molecular weight Broaden Your Horizon [6]

7 SYLLABUS CUM COM./XI/03 4 (c) In an ideal gas, there is no force of attraction between molecules. Hence, no heat is lost in the expansion. Q35. H (g) + O (g) H O(l) BE (H H) = x ; BE (O = O) = x BE (O H) = x 3 Latent heat of vaporisation of water liquid into water vapour = x 4, then f H (heat of formation of liquid water) is x (a) x + x - x 3 + x 4 (b) x 3 x - - x 4 x (c) x + x - x 3 x 4 (d) x + - x 3 + x 4 (c) H = (BF) reactant (BE) products [But all the species must be in gaseous state. In product, [H O(l) H O(g)] H must be added. Hence, H (g) + O (g) H O(l) H = ( BE) H (BE = [(H) vap + (BE) O-H ] x = x + -[x 4 + x 3 ] H ) OO x = x + -x 4 x 3 Q36. If a certain mass of gas is made to undergo separately adiabatic and isothermal expansions to the same pressure, starting from the same initial conditions of temperature and pressure, then, as compared to that of isothermal expansion, in the case of adiabatic expansion, the final (a) olume and temperature will be higher. (b) olume and temperature will be lower. (c) emperature will be lower but the final volume will be higher. (d) olume will be lower but the final temperature will be higher. (b) Q37. he enthalpy of formation of hypothetical MgCl is -5 kj mol - and for MgCl is -64 kj mol -. What is the enthalpy of the disproportionation of MgCl. (a) 39 kj mol - (b) -39 kj mol - (c) -767 kj mol - (d) -57 kj mol - (b) (i) Mg(s) + Cl (g) MgCl (s) H = -64 (ii) Mg(s) + Cl (g) MgCl(s) H = - 5 (iii) MgCl MgCl + Mg H =? H = H - H = -64 (-5) = - 39 kj mol - Q38. he expression sub H Θ = fus H Θ + vap H Θ is true at all (a) emperature (b) ressures (c) emperatures and pressures (d) emperature and atm pressure conditions (d) Q39. he word standard in standard molar enthalpy change implies (a) emperature 98 K (b) ressure atm (c) emperature 98 K and pressure atm (d) All temperatures and all pressures (c) Standard state implies to atm pressure and 98 K temperature. S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Broaden Your Horizon [7]

8 SYLLABUS CUM COM./XI/03 4 Q40. For hypothetical reversible reaction /A (g) + 3/B (g) AB 3 (g); H = -0 kj if standard entropies of A, B, and AB 3 are 60, 40, and 50 J K - mol -, respectively. he above reaction will be equilibrium at (a) 400 K (b) 500 K (c) 50 K (d) 00 K (b) At equilibrium, S total = 0 S Θ - S R Θ = 0 Q4. Standard molar enthalpy of formation of CO is equal to (a) Zero (b) he standard molar enthalpy of combustion of gaseous carbon. (c) he sum of standard molar enthalpies of formation of CO and O (d) he standard molar enthalpy of combustion of carbon (graphite). (d) Standard molar enthalpy of formation CO and the standard molar enthalpy of combustion of carbon (graphite) refer to the same chemical equation: C(graphite) + O (g) CO (g) Q4. In thermodynamics, a process is called reversible when (a) he surroundings and system change into each other. (b) here is no boundary between the system and surroundings (c) he surroundings are always in equilibrium with the system. (d) he system changes into the surroundings spontaneously. (c) Q43. he products of combustion of an aliphatic thiol (RSH) at 98 K are (a) CO (g), H O(g), and SO (g) (c) CO (l), H O(l), and SO (g) (b) CO (g), H O(l), and SO (g) (d) CO (g), H O(l), and SO (l) (b) C H 5 SH + 9 O (g) CO (g) + 3H O(l) + SO (g) S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Single Integer ype Question Q44. Bond dissociation energy of XY, X, and Y (all diatomic molecules) are in the ratio of ::0.5 and H f of XY is -00 kj mol -. he bond dissociation energy of X is 00x. Find the value of x. (4) X Y XY; H = - 00 kj Let the bond dissociation energy of X, Y, and XY be a : a : a (the given ratio) kj mol -, respectively. a a a = a = x = 400 x = 4 Q45. he polymerisation of propene to linear polypropene is represented by the reaction n CH 3 CH CH CH CH 3 CH n where n has large integral value, the average enthalpies of bond dissociation for (C = C) and (C C) at 98 K are +590 and +33 kj mol -, respectively. he enthalpy of polymerisation is -360 kj mol -. Find the value of n. Broaden Your Horizon [8]

9 SYLLABUS CUM COM./XI/03 4 sol. (5) Energy released = Energy due to formation of two single bonds = 33 = 66 kj mol - of propene H polymerisation/mol = = - 7 kj mol - H polymerisation = - 7 n = N = 5 Q46. he lattice energy of solid KCl is 8 kcal mol - and the enthalpy of solution of KCl in H O is.0 kcal mol -. If the hydration enthalpies of K + and Cl - ions are in the ratio of : then the enthalpy of hydration of K + is -0x K cal mol -. Find the value of x. (6) KCl(s) K + (g) + Cl - (g), H = 8 kcal mol - KCl(s) + aq K + (aq) + Cl - (aq), H =.0 kcal mol - Let the enthalpy of hydration of K + is Cl kcal mol - K + (g) + aq K + (aq), H 3 = a Cl - (g) + aq Cl - (aq), H 4 = a H 3 = - H + H - H 4 ª = a 3ª = - 80, a = -60 hyd H Θ of K + = ª = - 60 = - 0-0x = - 0 x = 6 Q47. A heated iron block at 7C loses 300 J of heat to the surroundings which are at a temperature of 7. his process is 0.05x J K -. Find the value of x. qsys 300 (5) sys S = 73 7 sys = JK surr S = q sys surr = 300 JK 300 total S or universe S = sys S + surr S = JK x = 0.5 x = 5 S.C.O. 08 IInd floor, Sec-36 D Chandigarh, h.30085, Broaden Your Horizon [9]

Class XI Chapter 6 Thermodynamics Question 6.1: Choose the correct answer. A thermodynamic state function is a quantity (i) used to determine heat changes (ii) whose value is independent of path (iii)

More information

I. Multiple Choice Questions (Type-I)

I. Multiple Choice Questions (Type-I) I. Multiple Choice Questions (Type-I) 1. Thermodynamics is not concerned about. (i) energy changes involved in a chemical reaction. the extent to which a chemical reaction proceeds. the rate at which a

More information

Identify the intensive quantities from the following: (a) enthalpy (b) volume (c) refractive index (d) none of these

Identify the intensive quantities from the following: (a) enthalpy (b) volume (c) refractive index (d) none of these Q 1. Q 2. Q 3. Q 4. Q 5. Q 6. Q 7. The incorrect option in the following table is: H S Nature of reaction (a) negative positive spontaneous at all temperatures (b) positive negative non-spontaneous regardless

More information

Answers to Problem Sheet (a) spontaneous (b) nonspontaneous (c) nonspontaneous (d) spontaneous (e) nonspontaneous

Answers to Problem Sheet (a) spontaneous (b) nonspontaneous (c) nonspontaneous (d) spontaneous (e) nonspontaneous Answers to Problem Sheet 5 1. (a) spontaneous (b) nonspontaneous (c) nonspontaneous (d) spontaneous (e) nonspontaneous 2. (a) Heat will flow from the warmer block of iron to the colder block of iron until

More information

CHEM Thermodynamics. Entropy, S

CHEM Thermodynamics. Entropy, S hermodynamics Change in Change in Entropy, S Entropy, S Entropy is the measure of dispersal. he natural spontaneous direction of any process is toward greater dispersal of matter and of energy. Dispersal

More information

10 NEET 31 Years 11. The enthalpy of fusion of water is kcal/mol. The molar entropy change for the melting of ice at

10 NEET 31 Years 11. The enthalpy of fusion of water is kcal/mol. The molar entropy change for the melting of ice at 6 Thermodynamics. A gas is allowed to expand in a well insulated container against a constant external pressure of.5 atm from an initial volume of.50 L to a final volume of 4.50 L. The change in internal

More information

UNIT # 06 THERMODYNAMICS EXERCISE # 1. T i. 1. m Zn

UNIT # 06 THERMODYNAMICS EXERCISE # 1. T i. 1. m Zn UNI # 6 HERMODYNMIS EXERISE #. m Zn.S Zn.( f i + m H O.S H O.( f i (6.8 gm (.4 J/g ( f + 8 gm (4. J/g ( f [(6.8 (.4 + 8(4.] f (6.8 (.4 ( + (8 (4. ( (6.8(.4( (8(4.( f 97. (6.8(.4 (8(4.. U q + w heat absorb

More information

6.Thermodynamics. Some Important Points and Terms of the Chapter

6.Thermodynamics. Some Important Points and Terms of the Chapter 6.Thermodynamics Some Important Points and Terms of the Chapter 1. System and the Surroundings: A system in thermodynamics refers to that part of universe in which observations are made and remaining universe

More information

Page 1 of 11. Website: Mobile:

Page 1 of 11. Website:    Mobile: Class XI Chapter 6 Thermodynamics Chemistry Question 6.1: Choose the correct answer. A thermodynamic state function is a quantity (i) used to determine heat changes (ii) whose value is independent of path

More information

Class XI Chapter 6 Thermodynamics Chemistry

Class XI Chapter 6 Thermodynamics Chemistry Class XI Chapter 6 Chemistry Question 6.1: Choose the correct answer. A thermodynamic state function is a quantity (i) used to determine heat changes (ii) whose value is independent of path (iii) used

More information

Thermodynamics 1. Thermodynamics means flow of heat. This deals with the quantitative relationship existing between heat and other forms of energy in physicochemical transformations. 2. The four laws are

More information

For more info visit

For more info visit Basic Terminology: Terms System Open System Closed System Isolated system Surroundings Boundary State variables State Functions Intensive properties Extensive properties Process Isothermal process Isobaric

More information

THERMODYNAMICS. Topic: 5 Gibbs free energy, concept, applications to spontaneous and non-spontaneous processes VERY SHORT ANSWER QUESTIONS

THERMODYNAMICS. Topic: 5 Gibbs free energy, concept, applications to spontaneous and non-spontaneous processes VERY SHORT ANSWER QUESTIONS THERMODYNAMICS Topic: 5 Gibbs free energy, concept, applications to spontaneous and non-spontaneous processes 1. What is Gibbs energy? VERY SHORT ANSWER QUESTIONS Gibbs energy (G): The amount of energy

More information

U = 4.18 J if we heat 1.0 g of water through 1 C. U = 4.18 J if we cool 1.0 g of water through 1 C.

U = 4.18 J if we heat 1.0 g of water through 1 C. U = 4.18 J if we cool 1.0 g of water through 1 C. CHAPER LECURE NOES he First Law of hermodynamics: he simplest statement of the First Law is as follows: U = q + w. Here U is the internal energy of the system, q is the heat and w is the work. CONVENIONS

More information

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.

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. , S is the measure of dispersal. The natural spontaneous direction of any process is toward greater dispersal of matter and of energy. Dispersal of matter: Thermodynamics We analyze the constraints on

More information

Ch 10 Practice Problems

Ch 10 Practice Problems Ch 10 Practice Problems 1. Which of the following result(s) in an increase in the entropy of the system? I. (See diagram.) II. Br 2(g) Br 2(l) III. NaBr(s) Na + (aq) + Br (aq) IV. O 2(298 K) O 2(373 K)

More information

(D) energy arising by gravitational pull. (A) molar internal energy (B) volume (C) w (D) q + w 7. For a monatomic gas, the value of the ratio of C p.

(D) energy arising by gravitational pull. (A) molar internal energy (B) volume (C) w (D) q + w 7. For a monatomic gas, the value of the ratio of C p. EXERCISE-01 CHECK YOUR GRASP SELEC HE CORREC ALERNAIVE (ONLY ONE CORREC ANSWER) 1. he piece of zinc at a temperature of 0.0 C weighing 65.38 g is dropped into 180 g of boiling water ( = 100 C). he specific

More information

BCIT Fall Chem Exam #2

BCIT Fall Chem Exam #2 BCIT Fall 2017 Chem 3310 Exam #2 Name: Attempt all questions in this exam. Read each question carefully and give a complete answer in the space provided. Part marks given for wrong answers with partially

More information

SPONTANEOUS PROCESSES AND THERMODYNAMIC EQUILIBRIUM

SPONTANEOUS PROCESSES AND THERMODYNAMIC EQUILIBRIUM 13 CHAPER SPONANEOUS PROCESSES AND HERMODYNAMIC EQUILIBRIUM 13.1 he Nature of Spontaneous Processes 13.2 Entropy and Spontaneity: A Molecular Statistical Interpretation 13.3 Entropy and Heat: Macroscopic

More information

Chemistry 1A, Spring 2008 Midterm Exam III, Version A April 14, 2008 (90 min, closed book)

Chemistry 1A, Spring 2008 Midterm Exam III, Version A April 14, 2008 (90 min, closed book) Chemistry 1A, Spring 2008 Midterm Exam III, Version A April 14, 2008 (90 min, closed book) Name: KEY SID: A Name: 1.) Write your name on every page of this exam. 2.) his exam has 15 multiple-choice questions

More information

The Second Law of Thermodynamics (Chapter 4)

The Second Law of Thermodynamics (Chapter 4) The Second Law of Thermodynamics (Chapter 4) First Law: Energy of universe is constant: ΔE system = - ΔE surroundings Second Law: New variable, S, entropy. Changes in S, ΔS, tell us which processes made

More information

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 11/8/2016 CHEM Thermodynamics. Change in Entropy, S. Entropy, S. Entropy, S S = S 2 -S 1. Entropy is the measure of dispersal. Entropy is the measure of dispersal. The natural spontaneous direction of any process is toward greater dispersal of matter and of energy. Dispersal of matter: Thermodynamics We analyze the constraints

More information

Downloaded from

Downloaded from THERMODYNAMICS Thermodynamics: is the branch of science which deals with deals with the study of different forms of energy and the quantitative relationship between them. Significance of Thermodynamics:

More information

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

4/19/2016. 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 information

THE ZEROTH AND FISRT LAW OF THERMODYNAMICS. Saeda Al-Mhyawi secend Tearm 1435H

THE ZEROTH AND FISRT LAW OF THERMODYNAMICS. Saeda Al-Mhyawi secend Tearm 1435H H ZROH AND FISR LAW OF HRMODYNAMIS Saeda Al-Mhyawi secend earm 435H HAR II H ZROH AND FISR LAW OF HRMODYNAMIS Lecture () Outline Introduction he Zeroth Law of hermodynamics he First Law of hermodynamics

More information

CHEMICAL THERMODYNAMICS

CHEMICAL THERMODYNAMICS CT 1 CHEMICAL THERMODYNAMICS Syllabus : Fundamentals of thermodynamics : System and surroundings, extensive and intensive properties, state functions, types of processes. First law of thermodynamics -

More information

Lecture 4. The Second Law of Thermodynamics

Lecture 4. The Second Law of Thermodynamics Lecture 4. The Second Law of Thermodynamics LIMITATION OF THE FIRST LAW: -Does not address whether a particular process is spontaneous or not. -Deals only with changes in energy. Consider this examples:

More information

Lecture #13. Chapter 17 Enthalpy and Entropy

Lecture #13. Chapter 17 Enthalpy and Entropy Lecture #13 Chapter 17 Enthalpy and Entropy First Law of Thermodynamics Energy cannot be created or destroyed The total energy of the universe cannot change Energy can be transferred from one place to

More information

Thermodynamics- 1) Hess's law states that 1) The standard enthalpy of an overall reaction is the sum of the enthalpy changes in individual reaction. ) Enthalpy of formation of compound is same as the enthalpy

More information

evidyarthi.in Thermodynamics Q 1.

evidyarthi.in Thermodynamics Q 1. SUBJECTIVE PROBLEMS: Q 1. Thermodynamics The enthalpy for the following reaction ( H o ) at 25 o C are given below: (i) 1/2 H 2 (g) + 1/2 O 2 (g) OH(g) 10.06 kcal (ii) H 2 (g) 2H(g) 104.18 kcal (iii) O

More information

Entropy Changes & Processes

Entropy Changes & Processes Entropy Changes & Processes Chapter 4 of Atkins: he Second Law: he Concepts Section 4.3 Entropy of Phase ransition at the ransition emperature Expansion of the Perfect Gas Variation of Entropy with emperature

More information

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

CHEMICAL THERMODYNAMICS. Nature of Energy. ΔE = q + w. w = PΔV CHEMICAL HERMODYNAMICS Nature of Energy hermodynamics hermochemistry Energy (E) Work (w) Heat (q) Some Definitions Study the transformation of energy from one form to another during physical and chemical

More information

Chapter 2 First Law Formalism

Chapter 2 First Law Formalism Chapter 2 First Law Formalism 2.1 The Special Character of State Variables A gas can be characterized by a set of state variables. Some, such as temperature, pressure, and volume, are measured directly

More information

Chapter 19 Chemical Thermodynamics

Chapter 19 Chemical Thermodynamics Chapter 19 Chemical Thermodynamics Kinetics How fast a rxn. proceeds Equilibrium How far a rxn proceeds towards completion Thermodynamics Study of energy relationships & changes which occur during chemical

More information

Practice Examinations Chem 393 Fall 2005 Time 1 hr 15 min for each set.

Practice Examinations Chem 393 Fall 2005 Time 1 hr 15 min for each set. Practice Examinations Chem 393 Fall 2005 Time 1 hr 15 min for each set. The symbols used here are as discussed in the class. Use scratch paper as needed. Do not give more than one answer for any question.

More information

Module 5 : Electrochemistry Lecture 21 : Review Of Thermodynamics

Module 5 : Electrochemistry Lecture 21 : Review Of Thermodynamics Module 5 : Electrochemistry Lecture 21 : Review Of Thermodynamics Objectives In this Lecture you will learn the following The need for studying thermodynamics to understand chemical and biological processes.

More information

Entropy and Free Energy

Entropy and Free Energy Page 1 Entropy and Free Energy How to predict if a reaction can occur at a reasonable rate? KINEICS Chapter 17 How to predict if a reaction can occur, given enough time? HERMODYNAMICS 1 Objectives Spontaneity

More information

Thermodynamic Processes and Thermochemistry

Thermodynamic Processes and Thermochemistry General Chemistry Thermodynamic Processes and Thermochemistry 박준원교수 ( 포항공과대학교화학과 ) 이번시간에는! Systems, states, and processes The first law of thermodynamics: internal energy, work, and heat Heat capacity,

More information

Second law of thermodynamics

Second law of thermodynamics Second law of thermodynamics It is known from everyday life that nature does the most probable thing when nothing prevents that For example it rains at cool weather because the liquid phase has less energy

More information

Chemistry 5350 Advanced Physical Chemistry Fall Semester 2013

Chemistry 5350 Advanced Physical Chemistry Fall Semester 2013 Chemistry 5350 Advanced Physical Chemistry Fall Semester 2013 Name: Quiz 2: Chapters 3, 4, and 5 September 26, 2013 Constants and Conversion Factors Gas Constants: 8.314 J mol 1 K 1 8.314 Pa m 3 mol 1

More information

Chpt 19: Chemical. Thermodynamics. Thermodynamics

Chpt 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 information

First Law CML 100, IIT Delhi SS. The total energy of the system. Contribution from translation + rotation + vibrations.

First Law CML 100, IIT Delhi SS. The total energy of the system. Contribution from translation + rotation + vibrations. Internal Energy he total energy of the system. Contribution from translation + rotation + vibrations. Equipartition theorem for the translation and rotational degrees of freedom. 1/ k B Work Path function,

More information

CHEM 305 Solutions for assignment #4

CHEM 305 Solutions for assignment #4 CEM 05 Solutions for assignment #4 5. A heat engine based on a Carnot cycle does.50 kj of work per cycle and has an efficiency of 45.0%. What are q and q C for one cycle? Since the engine does work on

More information

I PUC CHEMISTRY CHAPTER - 06 Thermodynamics

I PUC CHEMISTRY CHAPTER - 06 Thermodynamics I PUC CHEMISTRY CHAPTER - 06 Thermodynamics One mark questions 1. Define System. 2. Define surroundings. 3. What is an open system? Give one example. 4. What is closed system? Give one example. 5. What

More information

Classes at: - Topic: Thermodynamics. = E v. = G f T 1

Classes at: - Topic: Thermodynamics. = E v. = G f T 1 PHYSICAL CHEMISTRY by: SHAILENDRA KR. Classes at: - SCIENCE TUTORIALS; Opp. Khuda Baksh Library, Ashok Rajpath, Patna PIN POINT STUDY CIRCLE; House No. 5A/65, Opp. Mahual Kothi, Alpana Market, Patna Topic:

More information

Thermodynamics I - Enthalpy

Thermodynamics I - Enthalpy Thermodynamics I - Enthalpy Tinoco Chapter 2 Secondary Reference: J.B. Fenn, Engines, Energy and Entropy, Global View Publishing, Pittsburgh, 2003. 1 Thermodynamics CHEM 2880 - Kinetics An essential foundation

More information

Unit 7 (B) Solid state Physics

Unit 7 (B) Solid state Physics Unit 7 (B) Solid state Physics hermal Properties of solids: Zeroth law of hermodynamics: If two bodies A and B are each separated in thermal equilibrium with the third body C, then A and B are also in

More information

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

Chapter 16. Thermodynamics. Thermochemistry Review. Calculating H o rxn. Predicting sign for H o rxn. Creative Commons License Chapter 16 Thermodynamics GCC CHM152 Creative Commons License Images and tables in this file have been used from the following sources: OpenStax: Creative Commons Attribution License 4.0. ChemWiki (CC

More information

THERMODYNAMICS READ THE INSTRUCTIONS CAREFULLY

THERMODYNAMICS READ THE INSTRUCTIONS CAREFULLY TERMOYNMIS RE TE INSTRUTIONS REFULLY. The test is of hours duration.. The maximum marks are 60.. This test consists of 47 questions. 4. For each question in Section, & you will be awarded marks if you

More information

Thermochemistry Chapter 4

Thermochemistry Chapter 4 Thermochemistry Chapter 4 Thermochemistry is the study of energy changes that occur during chemical reactions Focus is on heat and matter transfer between the system and the surroundings Energy The ability

More information

Chapter 19 Chemical Thermodynamics

Chapter 19 Chemical Thermodynamics Chapter 19 Chemical Thermodynamics Kinetics How fast a rxn. proceeds Equilibrium How far a rxn proceeds towards completion Thermodynamics Study of energy relationships & changes which occur during chemical

More information

UNIVERSITY OF TORONTO FACULTY OF APPLIED SCIENCE AND ENGINEERING TERM TEST 2 17 MARCH First Year APS 104S

UNIVERSITY OF TORONTO FACULTY OF APPLIED SCIENCE AND ENGINEERING TERM TEST 2 17 MARCH First Year APS 104S UNIERSIY OF ORONO Please mark X to indicate your tutorial section. Failure to do so will result in a deduction of 3 marks. U 0 U 0 FACULY OF APPLIED SCIENCE AND ENGINEERING ERM ES 7 MARCH 05 U 03 U 04

More information

Thermodynamics 1. Hot Milk in a thermos flask is an example for 1) Isolated system ) Open system 3) Closed system 4) Adiabatic system. In open system, system and surroundings exchange 1) Energy only )

More information

Chem 152 Final. You will have 1 hour and 50 minutes. Do not begin the exam until you are instructed to start. Best of luck.

Chem 152 Final. You will have 1 hour and 50 minutes. Do not begin the exam until you are instructed to start. Best of luck. Chem 152 Final Section: Name: You will have 1 hour and 50 minutes. Do not begin the exam until you are instructed to start. Best of luck. Question 1 /80 Question 2 /20 Question 3 /20 Question 4 /20 Question

More information

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

2/18/2013. Spontaneity, Entropy & Free Energy Chapter 16. The Dependence of Free Energy on Pressure Sample Exercises Spontaneity, Entropy & Free Energy Chapter 16 16.7 The Dependence of Free Energy on Pressure Why is free energy dependent on pressure? Isn t H, enthalpy independent of pressure at constant pressure? No

More information

Thermochemistry: Part of Thermodynamics

Thermochemistry: Part of Thermodynamics Thermochemistry: Part of Thermodynamics Dr. Vickie M. Williamson @vmwilliamson Student Version 1 Chemical Thermodynamics! Thermodynamics: study of the energy changes associated with physical and chemical

More information

Introductory Inorganic Chemistry

Introductory Inorganic Chemistry Introductory Inorganic Chemistry What is Inorganic Chemistry? As: 1s 2 2s 2 2p 6 3s 2 3p 6 4s 2 3d 10 4p 3 Classes of Inorganic Substances Elements Ionic Compounds Covalent Compounds Atomic/Molecular

More information

Lecture 7 Enthalpy. NC State University

Lecture 7 Enthalpy. NC State University Chemistry 431 Lecture 7 Enthalpy NC State University Motivation The enthalpy change ΔH is the change in energy at constant pressure. When a change takes place in a system that is open to the atmosphere,

More information

Disorder and Entropy. Disorder and Entropy

Disorder 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 information

CHAPTER THERMODYNAMICS

CHAPTER THERMODYNAMICS 54 CHAPTER THERMODYNAMICS 1. If ΔH is the change in enthalpy and ΔE the change in internal energy accompanying a gaseous reaction, then ΔHis always greater than ΔE ΔH< ΔE only if the number of moles of

More information

Chemical thermodynamics and bioenergetics

Chemical thermodynamics and bioenergetics Chemical thermodynamics and bioenergetics Thermodynamics is a branch of physics that studies energy, the forms of its transformation, and the laws controlling its properties. Basic Concepts and Definitions.

More information

Thermochemistry: Energy Flow and Chemical Reactions

Thermochemistry: Energy Flow and Chemical Reactions Thermochemistry: Energy Flow and Chemical Reactions Outline thermodynamics internal energy definition, first law enthalpy definition, energy diagrams, calorimetry, theoretical calculation (heats of formation

More information

Chemistry 123: Physical and Organic Chemistry Topic 2: Thermochemistry

Chemistry 123: Physical and Organic Chemistry Topic 2: Thermochemistry Recall the equation. w = -PΔV = -(1.20 atm)(1.02 L)( = -1.24 10 2 J -101 J 1 L atm Where did the conversion factor come from? Compare two versions of the gas constant and calculate. 8.3145 J/mol K 0.082057

More information

Entropy Changes & Processes

Entropy Changes & Processes Entropy Changes & Processes Chapter 4 of Atkins: he Second Law: he Concepts Section 4.3, 7th edition; 3.3, 8th and 9th editions Entropy of Phase ransition at the ransition emperature Expansion of the Perfect

More information

AP Chemistry Chapter 16 Assignment. Part I Multiple Choice

AP Chemistry Chapter 16 Assignment. Part I Multiple Choice Page 1 of 7 AP Chemistry Chapter 16 Assignment Part I Multiple Choice 1984 47. CH 4 (g) + 2 O 2 (g) CO 2 (g) + 2 H 2 O(l) H = 889.1 kj H f H 2 O(l) = 285.8 kj mol 1 H f CO 2 (g) = 393.3 kj mol 1 What is

More information

TODAY 0. Why H = q (if p ext =p=constant and no useful work) 1. Constant Pressure Heat Capacity (what we usually use)

TODAY 0. Why H = q (if p ext =p=constant and no useful work) 1. Constant Pressure Heat Capacity (what we usually use) 361 Lec 7 Fri 9sep15 TODAY 0. Why H = q (if p ext =p=constant and no useful work) 1. Constant Pressure Heat Capacity (what we usually use) 2. Heats of Chemical Reactions: r H (mechanics of obtaining from

More information

Chemical Thermodynamics

Chemical Thermodynamics Page III-16-1 / Chapter Sixteen Lecture Notes Chemical Thermodynamics Thermodynamics and Kinetics Chapter 16 Chemistry 223 Professor Michael Russell How to predict if a reaction can occur, given enough

More information

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

Name 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 information

Exam 1 Solutions 100 points

Exam 1 Solutions 100 points Chemistry 360 Fall 018 Dr. Jean M. Standard September 19, 018 Name KEY Exam 1 Solutions 100 points 1.) (14 points) A chunk of gold metal weighing 100.0 g at 800 K is dropped into 100.0 g of liquid water

More information

What is thermodynamics? and what can it do for us?

What is thermodynamics? and what can it do for us? What is thermodynamics? and what can it do for us? The overall goal of thermodynamics is to describe what happens to a system (anything of interest) when we change the variables that characterized the

More information

Thermodynamic Third class Dr. Arkan J. Hadi

Thermodynamic Third class Dr. Arkan J. Hadi 5.5 ENTROPY CHANGES OF AN IDEAL GAS For one mole or a unit mass of fluid undergoing a mechanically reversible process in a closed system, the first law, Eq. (2.8), becomes: Differentiation of the defining

More information

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

Exam 2 Solutions. for a gas obeying the equation of state. Z = PV m RT = 1 + BP + CP 2, Chemistry 360 Dr. Jean M. Standard Fall 016 Name KEY 1.) (14 points) Determine # H & % ( $ ' Exam Solutions for a gas obeying the equation of state Z = V m R = 1 + B + C, where B and C are constants. Since

More information

Lecture 3 Evaluation of Entropy

Lecture 3 Evaluation of Entropy Lecture 3 Evaluation of Entropy If we wish to designate S by a proper name we can say of it that it is the transformation content of the body, in the same way that we say of the quantity U that it is the

More information

MUNISH KAKAR's INSTITUE OF CHEMISTRY

MUNISH KAKAR's INSTITUE OF CHEMISTRY ENTHALPY CHANGE & HESS's LAW ( WS #4 ) Q1. H and E for the reaction, S(s) + 3 O(g) SO3(g) are related as: (a) H = E 0.5 RT (b) H = E 1.5RT (c) H = E + RT (d) H = E + 1.5 RT Q. The enthalpy of solution

More information

Chemical Thermodynamics

Chemical Thermodynamics Quiz A 42.8 ml solution of ammonia (NH 3 ) is titrated with a solution of 0.9713 M hydrochloric acid. The initial reading on the buret containing the HCl was 47.13 ml and the final reading when the endpoint

More information

OPEN CLOSED ISOLATED. Only energy can be exchanged between system & surrounding. eg. closed vessel

OPEN CLOSED ISOLATED. Only energy can be exchanged between system & surrounding. eg. closed vessel THERMODYNAMICS Limitations :- (1) Not applicable on microscopic system like, change inside an atoms. Or system having few molecules only. (2) deals only with initial & final state (does not deal with path

More information

Chapter 5 Thermochemistry

Chapter 5 Thermochemistry Chapter 5 Thermochemistry Learning Outcomes: Interconvert energy units Distinguish between the system and the surroundings in thermodynamics Calculate internal energy from heat and work and state sign

More information

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

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

More information

Section 9: Thermodynamics and Energy

Section 9: Thermodynamics and Energy Section 9: Thermodynamics and Energy The following maps the videos in this section to the Texas Essential Knowledge and Skills for Science TAC 112.35(c). 9.01 Law of Conservation of Energy Chemistry (11)(A)

More information

Homework Problem Set 8 Solutions

Homework 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

CY 102: Physical Chemistry End Semester May 3, 2004

CY 102: Physical Chemistry End Semester May 3, 2004 CY 102: Physical Chemistry End Semester May 3, 2004 Answer All Questions R = (8.314 J = 0.0821 atm dm 3 ) K -1 mol -1 Trouton s constant = 88 J K -1 mol -1 F = 96,500 Cmol -1. Question 1: Fill in the blanks

More information

ENTHALPY OF DISPLACEMENT

ENTHALPY OF DISPLACEMENT QUESTIONSHEET 1 ENTHALPY OF DISPLACEMENT a) (i) 1 20 10-3 = 0.020 (1) (ii) 1.95/65 = 0.030 (1) b) 0.02(1) Zn in excess/equivalent mol in reaction(1) c) (i) to ensure heat equilibrium/balance/steady temperature(1)

More information

McCord CH301 Exam 5 Dec 5, 2017

McCord CH301 Exam 5 Dec 5, 2017 425 version last name first name signature McCord CH301 Exam 5 Dec 5, 2017 50070 BUR 106 Tuesday TTh 9:30 am - 11 pm Remember to refer to the Periodic Table handout that is separate from this exam copy.

More information

Enthalpies of Reaction

Enthalpies of Reaction Enthalpies of Reaction Enthalpy is an extensive property Magnitude of H is directly related to the amount of reactant used up in a process. CH 4 (g) + 2O 2 (g) CO 2 (g) + 2H 2 O(l) H = 890 kj 2CH 4 (g)

More information

THERMODYNAMICS. Extensive properties Intensive properties

THERMODYNAMICS. Extensive properties Intensive properties Thermodynamics The branch of chemistry deals with the energy change associated with chemical reactions is called chemical thermodynamics. System and surrounding A system may be defined as the specified

More information

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

Chapter 17. Free Energy and Thermodynamics. Chapter 17 Lecture Lecture Presentation. Sherril Soman Grand Valley State University Chapter 17 Lecture Lecture Presentation Chapter 17 Free Energy and Thermodynamics Sherril Soman Grand Valley State University First Law of Thermodynamics You can t win! The first law of thermodynamics

More information

Advanced Chemistry Practice Problems

Advanced Chemistry Practice Problems Thermodynamics: Review of Thermochemistry 1. Question: What is the sign of DH for an exothermic reaction? An endothermic reaction? Answer: ΔH is negative for an exothermic reaction and positive for an

More information

LECTURE 4 Variation of enthalpy with temperature

LECTURE 4 Variation of enthalpy with temperature LECTURE 4 Variation of enthalpy with temperature So far, we can only work at 25 C. Like c v we define a constant pressure heat capacity, c p, as the amount of heat energy needed to raise the temperature

More information

Homework Week 8 G = H T S. Given that G = H T S, using the first and second laws we can write,

Homework Week 8 G = H T S. Given that G = H T S, using the first and second laws we can write, Statistical Molecular hermodynamics University of Minnesota Homework Week 8 1. By comparing the formal derivative of G with the derivative obtained taking account of the first and second laws, use Maxwell

More information

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

5.2 Energy. N Goalby chemrevise.org Lattice Enthalpy. Definitions of enthalpy changes 5.2 Energy 5.2.1 Lattice Enthalpy Definitions of enthalpy changes Enthalpy change of formation The standard enthalpy change of formation of a compound is the energy transferred when 1 mole of the compound

More information

Chapter 6 Thermochemistry

Chapter 6 Thermochemistry Chapter 6 Thermochemistry Thermochemistry Thermochemistry is a part of Thermodynamics dealing with energy changes associated with physical and chemical reactions Why do we care? - Will a reaction proceed

More information

Entropy, Free Energy, and Equilibrium

Entropy, 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 information

Chem 75 Winter, 2017 Practice Exam 1

Chem 75 Winter, 2017 Practice Exam 1 This was Exam 1 last year. It is presented here with, first, just the problems and then with the problems and their solutions. YOU WILL BENEFIT MOST if you attempt first just the problems as if you were

More information

Entropy is a measure of the number of equivalent ways in which a system may exist.

Entropy is a measure of the number of equivalent ways in which a system may exist. Chapter 17 1 ENTROPY (S) Entropy is a measure of the number of equivalent ways in which a system may exist. S = Units: -23 k = Boltzmann constant ( 1.38 x 10 J/K) Ù = number of equivalent ways for the

More information

Chapter 19. Chemical Thermodynamics

Chapter 19. Chemical Thermodynamics Chapter 19. Chemical Thermodynamics 19.1 Spontaneous Processes Chemical thermodynamics is concerned with energy relationships in chemical reactions. We consider enthalpy and we also consider entropy in

More information

EQUILIBRIUM IN CHEMICAL REACTIONS

EQUILIBRIUM IN CHEMICAL REACTIONS EQUILIBRIUM IN CHEMICAL REACTIONS CHAPTER 12 Thermodynamic Processes and Thermochemistry CHAPTER 13 Spontaneous Processes and Thermodynamic Equilibrium CHAPTER 14 Chemical Equilibrium CHAPTER 15 Acid-Base

More information

120 [4] 2. C 6 H 11 OH + 8½O 2 6CO 2 + 6H 2 O/double or multiple equation (1) [1] 3. (a) by definition (1) 1

120 [4] 2. C 6 H 11 OH + 8½O 2 6CO 2 + 6H 2 O/double or multiple equation (1) [1] 3. (a) by definition (1) 1 0.0. moles methane = = 6.5 0 () 6 kj evolved = 6.5 0 890 = 5.56 () 5.56 0 joules = (mc) T () 5.56 0 T = = 6. K () 0 []. C 6 H OH + 8½O 6CO + 6H O/double or multiple equation () []. (a) by definition ()

More information

Introduction to Chemical Thermodynamics. D. E. Manolopoulos First Year (13 Lectures) Michaelmas Term

Introduction to Chemical Thermodynamics. D. E. Manolopoulos First Year (13 Lectures) Michaelmas Term Introduction to Chemical Thermodynamics D. E. Manolopoulos First Year (13 Lectures) Michaelmas Term Lecture Synopsis 1. Introduction & Background. Le Chatelier s Principle. Equations of state. Systems

More information

1.8 Thermodynamics. N Goalby chemrevise.org. Definitions of enthalpy changes

1.8 Thermodynamics. N Goalby chemrevise.org. Definitions of enthalpy changes 1.8 Thermodynamics Definitions of enthalpy changes Enthalpy change of formation The standard enthalpy change of formation of a compound is the energy transferred when 1 mole of the compound is formed from

More information

Chapter 19 Chemical Thermodynamics

Chapter 19 Chemical Thermodynamics Chapter 19 Chemical Thermodynamics Spontaneous Processes Entropy and the Second Law of Thermodynamics The Molecular Interpretation of Entropy Entropy Changes in Chemical Reactions Gibbs Free Energy Free

More information