thermodynamics ii - ap chem solutions350.0 g of water at 25.00 o c. the maximum temperature of the...
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Thermodynamics II
Calorimetry Hess’s Law
Enthalpy or Formation
Lecture 16
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Four Methods for Finding ∆H
1) Calculate it using average bond enthalpies 2) Measure it using a calorimeter. 3) Calculate it using Hess’s Law. 4) Calculate it using enthalpies of formation
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Calorimetry • Calorimetry – The measurement of heat transfer • Calorimeter – A device used to determine the amount
of heat transferred Heat flow cannot be measured directly. We measure the temperature before and
after a reaction, and use that data to calculate heat transfer.
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Calorimetry • Specific Heat Capacity (c)
• The amount of heat required to raise the temperature of 1 g of a substance by 1 K.
• A large value for water (4.184 J/g•K) – It takes a lot of heat to increase the temperature of water.
• A small value for iron (0.45 J/g•K) – It takes much less heat to raise the temperature of iron.
q = m c ∆T Heat lost or gained
by a substance Mass of that
substance
Specific heat capacity of
that substance
Temperature change of
that substance
∆T = Tf - Ti Copyright © 2013, 2011, 2009, 2008 AP Chem Solutions. All rights reserved.
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Coffee Cup Calorimeter
Thermometer Stir Stick
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Coffee Cup Calorimetry When measuring the heat lost or gained in a
chemical reaction that takes place in a coffee cup calorimeter, we use the solution as the basis for our calculations.
q = m c ∆T
Heat lost or gained by the solution in
the reaction Mass of
the solution
Specific heat of the solution
4.184 J/g•K is often used if
concentrations are low.
Temperature change of the
solution
∆T = Tf - Ti
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Coffee Cup Calorimetry • The reactants and products are the system. • The water which they are dissolved in and
calorimeter make up the surroundings. • The heat lost or gained by the solution is equal
to the heat lost or gained by the reaction. e.g.) If you calculated qsolution to be +568 J, the solution
gained heat. This means the reaction was exothermic, as the heat gained by the solution is equal to the heat lost by the reaction (qrxn= -568 J).
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Ex1) A 97 g iron bar was heated to 143oC and placed in a coffee cup calorimeter containing 350.0 g of water at 25.00oC. The maximum temperature of the water was measured to be 28.40 oC.
a) How much heat was gained by the water? b) How much heat was lost by the iron bar? c) What is the specific heat of iron?
Ex1) Calorimetry
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a) How much heat was gained by the water?
b) How much heat was lost by the iron bar?
Ex1) Calorimetry (cont.)
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a) How much heat was gained by the water?
b) How much heat was lost by the iron bar?
Ex1) Calorimetry (cont.)
wq mc T= ∆
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a) How much heat was gained by the water?
b) How much heat was lost by the iron bar?
Ex1) Calorimetry (cont.)
o o o(350.0 g)(4.184 J / g C)(28.40 C 25.00 C)w
w
q mc Tq
= ∆
= ⋅ −
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a) How much heat was gained by the water?
b) How much heat was lost by the iron bar?
Ex1) Calorimetry (cont.)
o o o(350.0 g)(4.184 J / g C)(28.40 C 25.00 C)4979 J
w
w
w
q mc Tqq
= ∆
= ⋅ −= +
Gaining heat is endothermic
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a) How much heat was gained by the water?
b) How much heat was lost by the iron bar?
Ex1) Calorimetry (cont.)
o o o(350.0 g)(4.184 J / g C)(28.40 C 25.00 C)4979 J
w
w
w
q mc Tqq
= ∆
= ⋅ −= +
Fewq q= −
Gaining heat is endothermic
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a) How much heat was gained by the water?
b) How much heat was lost by the iron bar?
Ex1) Calorimetry (cont.)
o o o(350.0 g)(4.184 J / g C)(28.40 C 25.00 C)4979 J
w
w
w
q mc Tqq
= ∆
= ⋅ −= +
Fe
Fe 4979 Jwq q
q= −= −
As energy is conserved, the heat gained by the water is equal in magnitude to the heat lost by the iron bar.
Gaining heat is endothermic
Losing heat is exothermic
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c) What is the specific heat of iron?
Ex1) Calorimetry (cont.)
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Ex1) Calorimetry (cont.)
Feq mc T= ∆
c) What is the specific heat of iron?
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Ex1) Calorimetry (cont.)
Fe
Fe
q mc Tqc
m T
= ∆
=∆
c) What is the specific heat of iron?
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Ex1) Calorimetry (cont.)
Fe
Fe
o o
4979 J(97 g)(28.40 C 143 C)
q mc Tqc
m T
c
= ∆
=∆
−=
−
c) What is the specific heat of iron?
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Ex1) Calorimetry (cont.)
Fe
Fe
o o
o
4979 J(97 g)(28.40 C 143 C)0.45 J / g C
q mc Tqc
m T
c
c
= ∆
=∆
−=
−
= ⋅
c) What is the specific heat of iron?
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Ex2) When 20.0 mL of 1.00 M NaCl at 22.00oC is mixed with 20.0 mL of 1.00 M AgNO3 at 22.00oC in a calorimeter, a white precipitate forms and the temperature of the mixture reaches 29.60oC. Assume that the specific heat capacity of the mixture is 4.184 J/g•K, its density is 1.00 g/mL, and the volumes are additive.
a) Write the net ionic equation for this reaction. b) Calculate ΔH for the reaction.
Ex2) Calorimetry
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Ex2) When 20.0 mL of 1.00 M NaCl at 22.00oC is mixed with 20.0 mL of 1.00 M AgNO3 at 22.00oC in a calorimeter, a white precipitate forms and the temperature of the mixture reaches 29.60oC. Assume that the specific heat capacity of the mixture is 4.184 J/g•K, its density is 1.00 g/mL, and the volumes are additive.
a) Write the net ionic equation for this reaction. b) Calculate ΔH for the reaction.
Ag+ (aq) + Cl- (aq) AgCl (s)
Ex2) Calorimetry
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Step 1) Calculate qsol. Step 2) Calculate qrxn.
Ex2) Calorimetry (cont.)
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Step 1) Calculate qsol. Step 2) Calculate qrxn.
Ex2) Calorimetry (cont.)
solq mc T= ∆
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Step 1) Calculate qsol. Step 2) Calculate qrxn.
Ex2) Calorimetry (cont.)
o o o(40.0 g)(4.184 J / g C)(29.60 C 22.00 C)sol
sol
q mc Tq
= ∆
= ⋅ −
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Step 1) Calculate qsol. Step 2) Calculate qrxn.
Ex2) Calorimetry (cont.)
o o o
o o
(40.0 g)(4.184 J / g C)(29.60 C 22.00 C)
(40.0 g)(4.184 J / g C)(7.60 C)
sol
sol
sol
q mc Tqq
= ∆
= ⋅ −
= ⋅
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Step 1) Calculate qsol. Step 2) Calculate qrxn.
Ex2) Calorimetry (cont.)
o o o
o o
(40.0 g)(4.184 J / g C)(29.60 C 22.00 C)
(40.0 g)(4.184 J / g C)(7.60 C)1270 J
sol
sol
sol
sol
q mc Tqqq
= ∆
= ⋅ −
= ⋅= +
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Step 1) Calculate qsol. Step 2) Calculate qrxn.
Ex2) Calorimetry (cont.)
1270 Jrxn sol
rxn
q qq
= −= −
The reaction is exothermic as heat is released to the water.
o o o
o o
(40.0 g)(4.184 J / g C)(29.60 C 22.00 C)
(40.0 g)(4.184 J / g C)(7.60 C)1270 J
sol
sol
sol
sol
q mc Tqqq
= ∆
= ⋅ −
= ⋅= +
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Step 3) Calculate Moles of Ag+or Cl-. Step 4) Calculate ΔHrxn.
Ex2) Calorimetry (cont.)
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Step 3) Calculate Moles of Ag+or Cl-. Step 4) Calculate ΔHrxn.
Ex2) Calorimetry (cont.)
1.0 moles Ag0.0200 L 0.0200 moles Ag1 L
++× =
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Step 3) Calculate Moles of Ag+or Cl-. Step 4) Calculate ΔHrxn.
Ex2) Calorimetry (cont.)
AgCl
1270 J0.0200 moles AgCl
rxnrxn
rxn
qHn
H
∆ =
−∆ =
1.0 moles Ag0.0200 L 0.0200 moles Ag1 L
++× =
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Step 3) Calculate Moles of Ag+or Cl-. Step 4) Calculate ΔHrxn.
Ex2) Calorimetry (cont.)
AgCl
1270 J0.0200 moles AgCl63500 J/mol 63.5 kJ/mol
rxnrxn
rxn
rxn
qHn
H
H
∆ =
−∆ =
∆ = − = −
1.0 moles Ag0.0200 L 0.0200 moles Ag1 L
++× =
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qrxn vs. ∆Hrxn
qrxn = The heat lost or gained in the experiment
that took place in the calorimeter ∆Hrxn = The heat lost or gained in the balanced
chemical equation
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Four Methods for Finding ∆H
1) Calculate it using average bond enthalpies. 2) Measure it using a calorimeter. 3) Calculate it using Hess’s Law. 4) Calculate it using enthalpies of formation.
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Hess’s Law
If a reaction is carried out in a series of steps, the overall change in enthalpy will be equal to the sum of the enthalpy changes for the individual steps.
• The overall enthalpy change will be the
same if a reaction is carried out in one step or in several steps.
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Ex1) Hess’s Law
Ex1) Calculate ∆H for the following reaction using the information in the table below.
4 NO2(g) + O2(g) 2 N2O5(s)
Reaction Chemical Equation Enthalpy Change 1 2 NO(g) + O2(g) N2O5(s) ∆H = - 223.7 kJ 2 2 NO(g) + O2(g) 2 NO2(g) ∆H = - 114.2 kJ
32
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Ex1) Hess’s Law (cont.)
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Ex1) Hess’s Law (cont.)
2(rxn 1) 4 NO(g) + 3 O2(g) 2 N2O5(s) ∆H = 2(- 223.7 kJ)
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Ex1) Hess’s Law (cont.)
2(rxn 1) 4 NO(g) + 3 O2(g) 2 N2O5(s) ∆H = 2(- 223.7 kJ) -2(rxn 2) 4 NO2(g) 4 NO(g) + 2 O2(g) ∆H = -2(-114.2 kJ)
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Ex1) Hess’s Law (cont.)
2(rxn 1) 4 NO(g) + 3 O2(g) 2 N2O5(s) ∆H = 2(- 223.7 kJ) -2(rxn 2) 4 NO2(g) 4 NO(g) + 2 O2(g) ∆H = -2(-114.2 kJ)
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Ex1) Hess’s Law (cont.)
2(rxn 1) 4 NO(g) + 3 O2(g) 2 N2O5(s) ∆H = 2(- 223.7 kJ) -2(rxn 2) 4 NO2(g) 4 NO(g) + 2 O2(g) ∆H = -2(-114.2 kJ) 4 NO2(g) + O2(g) 2 N2O5(s) ∆H = -219.0 kJ
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Ex2) Hess’s Law
Ex2) Calculate ∆H for the following reaction using the information in the table below.
3 C(s) + 4 H2(g) C3H8(g)
Reaction Chemical Equation Enthalpy Change 1 2 H2(g) + O2(g) 2 H2O(l) ∆H = - 571.7 kJ 2 C3H8(g) + 5O2(g) 3CO2(g) + 4H2O(l) ∆H = - 2220.1 kJ 3 C(s) + O2(g) CO2(g) ∆H = - 393.5 kJ
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Ex2) Hess’s Law (cont.)
2(rxn 1) 4 H2(g) + 2 O2(g) 4 H2O(l) ∆H = 2(- 571.7 kJ)
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Ex2) Hess’s Law (cont.)
2(rxn 1) 4 H2(g) + 2 O2(g) 4 H2O(l) ∆H = 2(- 571.7 kJ) -1(rxn 2) 3 CO2(g) + 4 H2O(l) C3H8(g) + 5 O2(g) ∆H = - (-2220.1kJ)
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Ex2) Hess’s Law (cont.)
2(rxn 1) 4 H2(g) + 2 O2(g) 4 H2O(l) ∆H = 2(- 571.7 kJ) -1(rxn 2) 3 CO2(g) + 4 H2O(l) C3H8(g) + 5 O2(g) ∆H = - (-2220.1kJ) 3(rxn 3) 3 C(s) + 3 O2(g) 3 CO2(g) ∆H = 3(- 393.5 kJ)
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Ex2) Hess’s Law (cont.)
2(rxn 1) 4 H2(g) + 2 O2(g) 4 H2O(l) ∆H = 2(- 571.7 kJ) -1(rxn 2) 3 CO2(g) + 4 H2O(l) C3H8(g) + 5 O2(g) ∆H = - (-2220.1kJ) 3(rxn 3) 3 C(s) + 3 O2(g) 3 CO2(g) ∆H = 3(- 393.5 kJ)
3 C(s) + 4 H2(g) C3H8(g) ∆H = -103.8 kJ
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Four Methods for Finding ∆H
1) Calculate it using average bond enthalpies. 2) Measure it using a calorimeter. 3) Calculate it using Hess’s Law. 4) Calculate it using enthalpies of formation.
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Standard Enthalpy of Formation
A hypothetical value that indicates how much heat would be lost or gained during the formation of one mole of a compound from the most common form of its elements in their standard states.
standard state (25oC, 1 atm)
∆H Formation
of
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Standard Enthalpy of Formation
For Methanol
C(s) + 2 H2(g) + ½ O2(g) CH3OH(g)
∆H = -201 kJ/mol of
Heat of formation reactions are always written so that all reactants exist as they would under standard
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Enthalpy of Formation
The ∆H value for the most stable form of any element in its standard state is zero.
Element ∆H Element ∆H Ca(s) 0 Cl2(g) 0 Ag(s) 0 H2(g) 0 Na(s) 0 Fe(s) 0 O2(g) 0 N2(g) 0
of
of
of
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Formula for Calculating the Enthalpy of a Reaction under
Standard Conditions ∆H = Σ n ∆H (products) – Σ n ∆H (reactants)
Sum of stoichiometric coefficients
o rxn
of
of
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Ex1) Enthalpy of Formation Ex1) Find ∆H for the thermite reaction under
standard conditions. Fe2O3(s) + 2 Al(s) 2 Fe(s) + Al2O3(s)
∆H = Σ n ∆H (products) – Σ n ∆H (reactants)
∆H = [2 (∆H (Fe(s))) + 1 (∆H (Al2O3(s)))] – [2 (∆H (Al(s))) + 1 (∆H (Fe2O3(s)))]
∆H = [2(0) + 1(-1675.7)] - [2(0) + 1(-821.4)] ∆H = - 854.3 kJ/mol
o rxn
of
of
o rxn
o rxn o
f of
of
of
o rxn o rxn
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Ex2) Enthalpy of Formation Ex2) Find ∆H for this reaction at standard
conditions. 2 H2S(g) + 3 O2(g) 2 SO2(g) + 2 H2O(g)
∆H = Σ n ∆H (products) – Σ n ∆H (reactants)
o rxn
of
of
o rxn
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Ex2) Enthalpy of Formation Ex2) Find ∆H for this reaction at standard
conditions. 2 H2S(g) + 3 O2(g) 2 SO2(g) + 2 H2O(g)
∆H = Σ n ∆H (products) - Σ n ∆H (reactants)
∆H = [2 (∆H (SO2(g))) + 2 (∆H (H2O(g)))] – [2 (∆H (H2S(g))) + 3 (∆H (O2(g)))]
o rxn
of
of
o rxn
o rxn o
f of
of
of
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Ex2) Enthalpy of Formation Ex2) Find ∆H for this reaction at standard
conditions. 2 H2S(g) + 3 O2(g) 2 SO2(g) + 2 H2O(g)
∆H = Σ n ∆H (products) - Σ n ∆H (reactants)
∆H = [2 (∆H (SO2(g))) + 2 (∆H (H2O(g)))] – [2 (∆H (H2S(g))) + 3 (∆H (O2(g)))]
∆H = [2(-296.8) + 2(-241.8)] - [2(-20.2) + 3(0)] ∆H = - 1036.8 kJ/mol
o rxn
of
of
o rxn
o rxn o
f of
of
of
o rxn o rxn
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Reaction kJ/mol
Elemental metal 1st used
by humans
2 Au(s) + 3/2 O2 (g) Au2O3(s) +131 ~6000 BCE
2 Ag(s) + 1/2 O2 (g) Ag2O(s) – 31 ~4000 BCE
Cu(s) + 1/2 O2 (g) CuO(s) – 156 ~4000 BCE
Pb(s) + 1/2 O2 (g) PbO(s) – 217 ~3500 BCE
Sn(s) + O2 (g) SnO2(s) – 581 ~1800 BCE
2 Fe(s) + 3/2 O2 (g) Fe2O3(s) – 822 ~1200 BCE
Enthalpy of Formation ofH∆
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Ex3) Enthalpy of Formation Ex3) Use the enthalpy of formation values below to
determine ΔHrxn for the reaction between C(s) and Fe2O3(s) to produce Fe(s).
2 Fe(s) + 3/2 O2 (g) Fe2O3(s)
C(s) + O2 (g) CO2(s)
822 kJ/molofH∆ = −
394 kJ/molofH∆ = −
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Ex3) Enthalpy of Formation Ex3) Use the enthalpy of formation values below to
determine ΔHrxn for the reaction between C(s) and Fe2O3(s) to produce Fe(s).
2 Fe(s) + 3/2 O2 (g) Fe2O3(s)
C(s) + O2 (g) CO2(s) – 2(rxn 1) 2 Fe2O3(s) 4 Fe(s) + 3 O2 (g) ∆H = – 2(– 822 kJ)
822 kJ/molofH∆ = −
394 kJ/molofH∆ = −
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Ex3) Enthalpy of Formation Ex3) Use the enthalpy of formation values below to
determine ΔHrxn for the reaction between C(s) and Fe2O3(s) to produce Fe(s).
2 Fe(s) + 3/2 O2 (g) Fe2O3(s)
C(s) + O2 (g) CO2(s) – 2(rxn 1) 2 Fe2O3(s) 4 Fe(s) + 3 O2 (g) ∆H = – 2(– 822 kJ) 3(rxn 2) 3 C(s) + 3 O2 (g) 3 CO2(s) ∆H = 3( – 394 kJ)
822 kJ/molofH∆ = −
394 kJ/molofH∆ = −
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Ex3) Enthalpy of Formation Ex3) Use the enthalpy of formation values below to
determine ΔHrxn for the reaction between C(s) and Fe2O3(s) to produce Fe(s).
2 Fe(s) + 3/2 O2 (g) Fe2O3(s)
C(s) + O2 (g) CO2(s) – 2(rxn 1) 2 Fe2O3(s) 4 Fe(s) + 3 O2 (g) ∆H = – 2(– 822 kJ) 3(rxn 2) 3 C(s) + 3 O2 (g) 3 CO2(s) ∆H = 3( – 394 kJ) 2 Fe2O3(s) + 3 C(s) 4 Fe(s) + 3 CO2(s) ∆H = + 462 kJ
822 kJ/molofH∆ = −
394 kJ/molofH∆ = −
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Ex) Enthalpy and Stoichiometry
2 H2O2(aq) O2(g) + 2 H2O(l) ∆H = -186 kJ Ex) How much heat is released when 3.56 g H2O2(aq)
decomposes into water and oxygen gas?
There are 2 moles H2O2 in the balanced equation.
2 22 2
2 2 2 2
1 mol H O 186 kJ3.56g H O 9.73 kJ34.02 g H O 2 mol H O
−× × = −
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