q= (10.0g 2.09j/g o c 15.0 o c) + (10.0g 333j/g)

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EXAMPLE: How much heat is required to heat 10.0 g of ice at -15.0 o C to steam at 127.0 o C ? q overall = q ice + q fusion + q water + q boil + q steam. q= (10.0g  2.09J/g o C  15.0 o C) + (10.0g  333J/g) + (10.0g  4.18J/g o C  100.0 o C) + (10.0g  2260J/g) - PowerPoint PPT Presentation

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EXAMPLE: How much heat is required to heat 10.0 g of ice at -15.0oC to steam at 127.0oC? qoverall = qice + qfusion + qwater + qboil + qsteam

q = (10.0g 2.09J/goC 15.0oC)

+ (10.0g 333J/g)

+ (10.0g 4.18J/goC 100.0oC)

+ (10.0g 2260J/g)

+ (10.0g 2.03J/goC 27.0oC)

q = (314 + 3.33×103 + 4.18×103 + 2.26×104 + 548)J

= 30.9 kJ

Heat Flow in Reactions

exothermic –reaction that gives off energy

q < 0

isolated system E=0 heat released by reaction raises the temperature of the solvent

constant T, heat is released to the surroundings

endothermic – reaction that absorbs energy

q > 0

Expansion Type Work

w = -PV system does work

P

P

Vinitial

V

V = Vfinal - Vinitial

qp = +2kJ

Do 250 J of work to compress a gas, 180 J of heat are released by the gas

What is E for the gas?

430

J70

J-7

0 J

-180

J

-250

J

0% 0% 0%0%0%

1. 430 J

2. 70 J

3. -70 J

4. -180 J

5. -250 J

0

0

130

10

Enthalpy HE = q + w

at constant V, wexpansion = 0

E = qv

at constant P, wexpansion = -PV

E = qp - PVDefinePV) = PV at constant P

Hence H = qp

EnthalpyEnthalpy heat at constant pressure or the

heat of reaction

qp = H = Hproducts - Hreactants

Exothermic ReactionH = (Hproducts - Hreactants) < 0

2 H2(g) + O2(g) 2 H2O(l) H < 0

Endothermic ReactionH = (Hproducts - Hreactants) > 0

2 H2O(l) 2 H2(g) + O2(g) H > 0

State FunctionsH and E along with P, T, V (or P, T,

V) and many others are state functions. They are the same no matter what path we take for the change.

• q and w are not state functions, they depend on which path we take between two points.

initial

final

Eq

w

q

wE=Efinal-Einitial

q and w can be anything

Path Independent Energy Changes

Which day would you like OWL quizzes due (4 AM)

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20

21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40

41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80

81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100

101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120

121 122 123 124 125 126 127 128 129 130

0% 0% 0%0%0%

1. Monday2. Tuesday3. Wednesday4. Thursday5. Friday

100

0

130

Stepwise Energy Changesin Reactions

Laws of Thermochemistry

1. The magnitude of is directly proportional to the amount of reaction.

H is for 1 mole of reaction as written

2 H2(g) + O2(g) 2 H2O(l) H = -571.6 kJ

H2(g) + ½ O2(g) H2O(l) H = -285.8 kJ

Can have ½ mole O2 just not ½ molecule

Laws of Thermochemistry

2. H for a reaction is equal in magnitude but opposite in sign to H for the reverse reaction.

H2(g) + ½ O2(g) H2O(l) H = -285.8 kJ

H2O(l) H2(g) + ½ O2(g) H = +285.8 kJ

Laws of Thermochemistry

3. The value of H for the reaction is the same whether it occurs directly or in a series of steps.

Hoverall = H1 + H2 + H3 + · · ·

also called Hess’ Law

Enthalpy Diagram

H2(g) + ½ O2(g) H2O(l) H = -285.8 kJ

H2O(l) H2O(g) H = +44.0 kJ

H2(g) + ½ O2(g) H2O(g) H = -241.8 kJ

Given 3 CO + 3/2 O2 3 CO2 H = -849 kJ

What is H for CO2 CO + ½ O2 ?

100

0

130

-283

kJ

+283

kJ

+849

kJ

-254

7 kJ

+254

7 kJ

0% 0% 0%0%0%

1. -283 kJ

2. +283 kJ

3. +849 kJ

4. -2547 kJ

5. +2547 kJ

Energy and Stoichiometry

• Since H is per mole of reaction we can relate heat to amount of reaction

• Given C2H6 + 7/2 O2 2 CO2 + 3 H2O H=-1559.7 kJ

• If 632.5 kJ are released to surroundings what mass of H2O is formed?

• 632.5 kJ released means H = -632.5 kJ for this much H2O

OHg92.21OHmol1

OHg016.18

reactionmol1

OHmol3

kJ7.1559

reactionmol1kJ5.632 2

2

22

Bomb Calorimeter measure qv

qrxn + qcal = 0qrxn = -qcal

qrxn = - ccalTErxn = qrxn/moles rxnErxn ≈ Hrxn

H = E + (PV)H = E + RTngas

@298K RT = 2.5 kJ/mol

“Coffee Cup” Calorimeter qp

Photo by George Lisensky

Measuring H

• When 25.0 mL of 1.0 M H2SO4 are added to 50.0 mL of 1.0 M KOH, both initially at 24.6C the temperature rises to 33.9C. What is H for H2SO4 + 2 KOH K2SO4 + 2 H2O ? (Assume d = 1.00 g/mL, c = 4.18 J/g.C)

• qsoln = mcT

• m = (25.0 + 50.0)mL×1.00g/mL = 75.0 g

Measuring H cont.

• q=mcT

• qsoln = 75.0 g × 4.18 J/g.C × (33.9-24.6)C

• qsoln = 2916 J

• qrxn + qsoln = 0

• qrxn = -2916 J

Hrxn = qrxn/moles rxn

Measuring H cont

• How many moles rxn?

• 1 mol rxn / 1 mol H2SO4

• 1 mol rxn / 2 mol KOH

4242 SOHmol025.0

mL1000

L1

L1

SOHmol00.1mL0.25

KOHmol050.0mL1000

L1

L1

KOHmol00.1mL0.50

Stoichiometric mixture so 0.025 mol rxn

Measuring H cont

Hrxn = qrxn/moles rxn

Hrxn = -2916 J / 0.025 mol rxn

Hrxn = -116622 J / mol rxn

Hrxn = -117 kJ

H is per mole of reaction as written

If excess Al is added to 50 mL of 0.250 M H2SO4 how many moles of

the following reaction occur?2 Al + 3 H2SO4 Al2(SO4)3 + 3 H2

10

0

0

130

0% 0% 0%0%0%

1. 0.0125 mol

2. 0.0375 mol

3. 0.025 mol

4. 0.00625 mol

5. 0.00417 mol

Hess’s Law

• Can find H for an unknown, or hard to measure, reaction by summing measured H values of known reactions.

EXAMPLE

H for formation of CO cannot readily be measured since a mixture of CO and CO2 is always formed.

C (s) + ½ O2 (g) CO (g) H = ?

C (s) + O2 (g) CO2 (g) H1 = -393.5 kJ

CO (g) + ½ O2 (g) CO2 (g) H2 = -283.0 kJ

C (s) + ½ O2 (g) CO (g) H = H1 - H2

H = H1 - H2 = -393.5 – (-283.0) = -110.5 kJ

Standard Enthalpy of Formation

the enthalpy associated with the formation of 1 mol of a substance from its constituent elements under standard state conditions at the specified temperature

For an element this is a null reaction

O2 (g) O2 (g) H = 0

Hf = 0 for all elements in their standard states

For which one of these reactions is ΔHºrxn

= ΔHºf?

0% 0% 0%0%0%

1. N2(g) + 3 H2(g) 2 NH3(g)

2. C(graphite) + 2 H2(g) CH4(g)

3. C(diamond) + O2(g) CO2(g)

4. CO(g) + ½ O2(g) CO2(g)

5. H2(g) + Cl2(g) 2 HCl(g)

100

0

130

Calculation of Ho

Ho = mols Hfoproducts – mols Hf

oreactants

We can always convert products and reactants to the elements.

Hess’s law says H is the same whether we go directly from reactants to products or go via elements

Example What is the value of Hrxn for the reaction:2 C6H6(l) + 15 O2(g) 12 CO2(g) + 6 H2O(g)

from Appendix J TextC6H6(l) Hf

o = + 49.0 kJ/mol

O2(g) Hfo = 0

CO2(g) Hfo = - 393.5

H2O(g) Hfo = - 241.8

Hrxn mols Hfoproduct

– mols Hforeactants

ExampleWhat is the value of Hrx for the reaction:2 C6H6(l) + 15 O2(g) 12 CO2(g) + 6 H2O(g)

from Appendix J TextC6H6(l) Hf

o = + 49.0 kJ/mol; O2(g) Hfo = 0

CO2(g) Hfo = - 393.5; H2O(g) Hf

o = - 241.8 Hrxn molsHf

oproduct - mols Hf

oreactants

Hrxn - 393.5) + 6(- 241.8)product

- 2(+ 49.0 ) + 15(0)reactants kJ/mol

= - 6.2708 103 kJ

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