Chang CH06 Thermochemistry

CHM031 Lesson 4
Thermochemistry
(Chapter 6)
© McGraw-Hill Education. All rights reserved. Authorized only for instructor use in the classroom. No reproduction or
further distribution permitted without the prior written consent of McGraw-Hill Education.
Learning
Outcomes
• Write thermochemical equations
and compute the enthalpy of a
reaction.
• Compute the stoichiometric

amounts of products, reactants
and enthalpies involved in a
chemical reaction.
• Compute heats of reaction from

calorimetry data.
• Compute the enthalpy of reaction

from the standard enthalpies of
formation using Hess's law.
© 2019 McGraw-Hill Education. 6-3
Energy
Energy is the capacity to do work.

• Radiant energy comes from the sun and is earth’s primary
energy source
• Thermal energy is the energy associated with the random
motion of atoms and molecules
• Chemical energy is the energy stored within the bonds of
chemical substances
• Nuclear energy is the energy stored within the collection of
neutrons and protons in the atom
• Potential energy is the energy available by virtue of an
object’s position
© McGraw-Hill Education. 6-4

Law of conservation
of energy:
The total quantity of
energy in the
universe is assumed
constant.

Laws of energy - U.S. Energy Information Administration (EIA)
Energy Changes in Chemical Reactions
• Heat is the transfer of thermal

energy between two bodies
that are at different
temperatures
• Temperature is a measure of
the thermal energy.
• “heat absorbed” or
“heat released”
Japanese research tells us what colours of clothing are6-12

© McGraw-Hill Education. cooler
in hot weather (yahoo.com)
Energy Changes in Chemical Reactions
• Heat is the transfer of thermal

energy between two bodies
that are at different
temperatures
• Temperature is a measure of
the thermal energy.
• “heat absorbed” or
“heat released”
Japanese research tells us what colours of clothing are6-13

© McGraw-Hill Education. cooler
in hot weather (yahoo.com)
Thermochemistry
Thermochemistry is the study of heat
change in chemical reactions.
The system is the specific part of the

universe that is of interest in the study.
5.2 Calorimetry – Chemistry (pressbooks.pub)
3 types of systems
Jump to long description

Exothermic and Endothermic Processes
Exothermic process is any process that gives off heat –

transfers thermal energy from the system to the surroundings.
2H 2 ( g ) + O 2 ( g ) → 2H 2O ( l ) + energy
H 2O ( g ) → H 2O ( l ) + energy
Endothermic process is any process in which

heat has to be supplied to the system from the
surroundings.
energy + 2HgO ( s ) → 2Hg ( l ) + O 2 ( g )
energy + H 2O ( s ) → H 2O ( l )
Schematic of Exothermic and Endothermic
Processes

Thermodynamics (1 of 2)
Thermodynamics is the scientific study of the interconversion of heat
and other kinds of energy.
State functions are properties that are determined by the state of the
system, regardless of how that condition was achieved.
energy, pressure, volume, temperature
ΔU = U final − U initial
ΔP = Pfinal − Pinitial
ΔV = Vfinal − Vinitial
ΔT = Tfinal − Tinitial
Potential energy of hiker 1 and hiker 2 is
the same even though they took different
paths. Jump to long description
Thermodynamics (2 of 2)
First law of thermodynamics – energy can be converted

from one form to another, but cannot be created or destroyed.
ΔU system + ΔU surroundings = 0
or
ΔU system = − ΔU surroundings
C3 H 8 + 5O2 → 3CO2 + 4 H 2O
Exothermic chemical reaction!
Chemical energy lost by Energy gained by the

=
combustion system surroundings

Another form of the first law for
ΔU = q + w
ΔU is the change in internal energy of a system

q is the heat exchange between the system and the surroundings
w is the work done on (or by) the system
w = − PΔ V when a gas expands against a constant external pressure
Table 6.1 Sign Conventions for Work and Heat

Process Sign
Work done by the system on the surroundings −
Work done on the system by the surroundings
Heat absorbed by the system from the surroundings

(endothermic process)
Heat absorbed by the surroundings from the system

−
(exothermic process)

Work Done on the System
w = F d ΔV > 0
w = − P V − PΔV  0
F wsys  0
P V = 2 d3 = F d = w
d
Work is
not a
state
function.

Example 6.1(1 of 4)
A certain gas expands in volume from 2.0 L to 6.0 L at

constant temperature.
Calculate the work done by the gas if it expands
(a) against a vacuum
(b) against a constant pressure of 1.2 atm

Example 6.1 (2 of 4)
Strategy
A simple sketch of the situation is helpful here:
The work done in gas expansion is equal to the product of the

external, opposing pressure and the change in volume.
What is the conversion factor between L · atm and J?

Solution
a) Because the external pressure is zero, no work is done in
the expansion.
w = − PV
= − ( 0 ) ( 6.0 − 2.0 ) L
=0
b) The external, opposing is 1.2 atm, so
w = − PV
= − (1.2 atm ) ( 6.0 − 2.0 ) L
= − 4.8L  atm

To convert the answer to joules, we write
101.3 J
w = − 4.8L  atm 
1 L  atm
= − 4.9  102 J
Check
Because this is gas expansion
(work is done by the system on
the surroundings), the work done
has a negative sign.

The work done when a gas is compressed in a cylinder like

that shown in Figure 6.5 is 462 J.
During this process, there is a heat transfer of 128 J from the

gas to the surroundings.
Calculate the energy change for this process.

Strategy
Compression is work done on the gas, so what is the sign for
w?
Heat is released by the gas to the surroundings.
Is this an endothermic or exothermic process?
What is the sign for q?

Solution
To calculate the energy change of the gas, we need
Equation (6.1). Work of compression is positive and
because heat is released by the gas, q is negative.
Therefore, we have
ΔU = q + w
= − 128 J + 462 J
= 334 J
As a result, the energy of the gas increases by 334 J.

Chemistry in Action: Inflating Bicycle Tire
ΔU = q + w
q=0
w  0, ΔU  0
ΔU = C Δ T
ΔT  0, SNOW!

Enthalpy and the First Law of
Thermodynamics
ΔU = q + w
At constant pressure:
q = Δ H and w = − P Δ V
Δ U = ΔH − P Δ V
Δ H = ΔU + P ΔV

Enthalpy
Enthalpy (H) is used to quantify the heat flow into or out of a system in a
process that occurs at constant pressure.
Δ H = H ( products ) − H ( reactants )
ΔH = heat given off or absorbed during a reaction at constant pressure
H products  H reactants H products  H reactants

ΔH 0 ΔH 0
Thermochemical Equations (1 of 4)
Is ΔH negative or positive?
System absorbs heat
Endothermic
H  0
6.01 kJ are absorbed for every 1mole of ice that melts
at 0 C and 1 atm.
H2O ( s ) → H2O (l )
Is ΔH negative or positive?
System gives off heat
Exothermic
ΔH  0
890.4 kJ are released for every 1 mole of methane that

is combusted at 25 C and 1 atm.
CH 4 ( g ) + 2O 2 → CO 2 ( g ) + 2H 2 O ( l )

The stoichiometric coefficients always refer to the number

of moles of a substance
H2O ( s ) → H2O (l ) ΔH = 6.01kJ mol
If you reverse a reaction, the sign of H changes.

H2O ( l ) → H2O ( s ) ΔH = − 6.01 kJ mol
If you multiply both sides of the equation by a factor n,

then ΔH must change by the same factor n.
2H 2 O ( s ) → 2H 2 O ( l ) ΔH = 2  6.01 = 12.0kJ

The physical states of all reactants and products must

be specified in thermochemical equation.
H 2O ( s ) → H 2O ( l ) H = 6.01 kJ mol
H 2O ( l ) → H 2O ( g ) H = 44.0 kJ mol

Example 6.3
Solution
We need to first calculate the number of moles of SO2 in 87.9 g of
the compound and then find the number of kilojoules produced
from the exothermic reaction. The sequence of conversions is as
follows:
gram of SO 2 → moles of SO 2 → kilojoules of heat generated
Therefore, the enthalpy change for this reaction is given by

1 mol SO 2 −198.2 kJ
ΔH = 87.9 g SO 2  
64.07g SO 2 2 mol SO 2
= −136 kJ
and the heat released to the surroundings is 136 kJ.
Example 6.3
Check
Because 87.9 g is less than twice the molar mass of So2
(2  64.07 g) as shown in the preceding thermochemical
equation, we expect the heat released to be smaller than
198.2 kJ.

Specific Heat and Heat Capacity
The specific heat(s) of a substance is the amount of heat (q) required to
raise the temperature of one gram of the substance by one degree
Celsius.
Table 6.2 The Specific Heats of The heat capacity (C) of a substance is the
Some Common Substances amount of heat (q) required to raise the
temperature of a given quantity (m) of the
substance by one degree Celsius.
C = m s
Heat (q) absorbed or released:
q = m  s  Δt
q = C  Δt
Δt = t final − t initial
A 466-g sample of water is heated from 8.50C to 74.60C.
Calculate the amount of heat absorbed (in kilojoules) by

the water.

Strategy
We know the quantity of water and the specific heat of water. With this
information and the temperature rise, we can calculate the amount of heat
absorbed (q).
Solution
Using Equation (6.12), we write
q = ms Δt
= ( 466 g ) ( 4.184 J g  C ) ( 74.60 C − 8.50 C )
1 kJ
= 1.29  105 J 
1000 J
= 129 kJ
Check
The units g and º C cancel, and we are left with the desired unit kJ. Because heat
is absorbed by the water from the surroundings, it has a positive sign.
Constant-Volume Calorimetry
bomb calorimeter q sys = q water + q bomb + q rxn
q sys = 0
q rxn = − ( q water + q bomb )
q water = m  s  Δt
q bomb = Cbomb  Δt
Reaction at Constant V
ΔH  qrxn
No heat enters or leaves! ΔH ~ qrxn

A quantity of 1.435 g of naphthalene

(C10H8) a pungent-smelling substance used
in moth repellents, was burned in a
constant-volume bomb calorimeter.
Consequently, the temperature of the water

rose from 20.28 C to 25.95C
C10 H8
If the heat capacity of the bomb plus water
was 10.17 kJ/C, calculate the heat of
combustion of naphthalene on a molar
basis; that is, find the molar heat of
combustion.

Strategy
Knowing the heat capacity and the temperature rise, how do
we calculate the heat absorbed by the calorimeter?
What is the heat generated by the combustion of 1.435 g of

naphthalene?
What is the conversion factor between grams and moles of

naphthalene?

Solution
The heat absorbed by the bomb and water is equal to
the product of the heat capacity and the temperature
change.
From Equation (6.16), assuming no heat is lost to the
surroundings, we write qcal = Ccal Δt
= (10.17KJ C )( 25.95 C − 20.28 C )
= 57.66 kJ
Because qsys = qcal + qrxn = 0, qcal = − qrxn.
The heat change of the reaction is −57.66 kJ. This is the heat released
by the combustion of 1.435 g of C10H8; therefore, we can write the
conversion factor as
−57.66 kJ
1.435 g C10 H8

The molar mass of naphthalene is 128.2 g, so the heat of

combustion of 1 mole of naphthalene is
−57.66 kJ 128.2 g C 10 H 8
molar heat of combustion = 
1.435 g C 10 H8 1 mol C10 H8
= −5.151 103 kJ mol

Constant-Pressure Calorimetry
“coffee cup” calorimeters q sys = q water + q cal + q rxn

q sys = 0
q rxn = − ( q water + q cal )
q water = m  s  Δt
Reaction at Constant P
ΔH = qrxn

No heat enters
or leaves!
Some Heats of Reaction
Table 6.3 Heats of Some Typical Reactions Measured at Constant

Pressure
Type of Reaction Example H

( kJ / mol )
Heat of neutralization HCl( aq ) + NaOH ( aq ) → NaCl ( aq ) + H 2O (l ) −56.2
Heat of ionization H 2O(l ) → H + ( aq ) + OH − ( aq ) 56.2
Heat of fusion H 2 O( s ) → H 2 O( l ) 6.01
Heat of vaporization H 2 O(l ) → H 2 O( g ) 44.0 *
Heat of reaction MgCl 2 ( s ) + 2Na (l ) → 2Nacl( s ) + Mg( s ) −180.2

A lead (Pb) pellet having a mass

of 26.47 g at 89.98 C was
placed in a constant-pressure
calorimeter of negligible heat
capacity containing 100.0 mL of
water.
The water temperature rose

from 22.50 C to 23.17 C.
What is the specific heat of the

lead pellet?

Strategy
A sketch of the initial and final situation is as follows:
We know the masses of water and the lead pellet as well as the initial and final
temperatures. Assuming no heat is lost to the surroundings, we can equate the
heat lost by the lead pellet to the heat gained by the water. Knowing the specific
heat of water, we can then calculate the specific heat of lead.

Solution
Treating the calorimeter as an isolated system (no heat lost to
the surroundings), we write
qpb + qH2 O = 0
or
qpb = − qH2 O
The heat gained by the water is given by
qH2 0 = ms Δ t
where m and s are the mass and specific heat and
Δt = tfinal − tinitial
Therefore,
qH2 O = (100.0 g ) ( 4.184J g  C ) ( 23.17 C − 22.50 C )

= 280.3 J
Because the heat lost by the lead pellet is equal to the heat
gained by the water, qPb = −280.3 J. Solving for the specific
heat of Pb, we write
qPb = msΔt
−280.3 J = ( 26.47g ) ( s ) ( 23.17 C − 89.98 C )
s = 0.158J g  C

A quantity of 1.00  10 mL of 0.500 M HCl was mixed with1.00  102

2
mL of 0.500M NaOH in a constant-pressure calorimeter of

negligible heat capacity. The initial temperature of the HCl and
NaOH solutions was the same, 22.50 C, and the final
temperature of the mixed solution was 25.86 C. Calculate the
heat change for the neutralization reaction on a molar basis:
NaOH ( aq ) + HCl ( aq ) → NaCl ( aq ) + H 2 O ( l )
Assume that the densities and specific heats of the solutions

are the same as for water
(1.00 g/ mL and 4.184 J/g∙°C, respectively)
Strategy
Because the temperature rose, the neutralization reaction
is exothermic.
How do we calculate the heat absorbed by the combined

solution?
What is the heat of the reaction?
What is the conversion factor for expressing the heat of

reaction on a molar basis?

Solution
Assuming no heat is lost to the surroundings,
qsys = qsoln + qrxn = 0,so qrxn = − qsoln , where qsoln
is the heat absorbed by the combined solution. Because the

density of the solution is 1.00 g/ mL, the mass of a 100-mL
solution is 100 g.
Thus,
qsoln = msΔt
= (1.00  102 g + 1.00  102 g ) ( 4.184 J g. C ) ( 25.86 C − 22.50c )
= 2.81×103 J
= −2.81 kJ.
Because qrxn = - qsoln , qrxn = - 2.81 kJ.

From the molarities given, the number of moles of both HCl and
NaOH in 1.00  102 mL solution is
0.500mol
 0.100L = 0.0500mol
1L
Therefore, the heat of neutralization when 1.00 mole of HCl
reacts with 1.00 mole of NaOH is
−2.81kJ
heat of neutralization = = −56.2 kJ mol
0.0500mol

Enthalpy of Formation
• Because there is no way to measure the absolute value of the
enthalpy of a substance, must I measure the enthalpy change for
every reaction of interest?
• Establish an arbitrary scale with the standard enthalpy of formation
( )
ΔH f0 as a reference point for all enthalpy expressions.
Standard enthalpy of formation ΔH f ( 0

)
is the heat change that results when one mole of a compound
is formed from its elements at a pressure of 1 atm
• The standard enthalpy of formation of any element in its most stable

form is zero.
ΔH f0 ( O 2 ) = 0 ΔH f0 ( C, graphite ) = 0
ΔH f0 ( O3 ) = 142 KJ mol ΔH f0 ( C, diamond ) = 1.90 KJ mol

Some
Standard
Enthalpies
of
Formation

Enthalpy of Reaction
The standard enthalpy of reaction ( ΔH 0 rxn )

is the enthalpy of a reaction carried out at 1 atm.
consider the hypothetical reaction: aA + bB → cC + dD
ΔH rxn
0
= cΔH f0 ( C ) + dΔH f0 ( D )  − aΔH f0 ( A ) + dΔH f0 ( B ) 
ΔH rxn
0
=  nΔH f0 ( products ) −  mΔH f0 ( reactants )



• Hess’s Law: When reactants are converted to products, the

change in enthalpy is the same whether the reaction takes
place in one step or in a series of steps.
• (Enthalpy is a state function. It doesn’t matter how you get

there, only where you start and end.)
• The enthalpy change would be the same whether the overall

reaction takes place in one step or many steps.

Calculate the standard enthalpy of formation of acetylene

(C2H2) from its elements:
2C ( graphite ) + H 2 ( g ) → C 2 H 2 ( g )
The equations for each step and the corresponding enthalpy

changes are
( a ) C ( graphite ) + O 2 ( g ) → CO 2 ( g ) 
ΔH rxn = −393.5 kJ / mol
1
( b ) H 2 ( g ) + O2 ( g ) → H 2O (l ) 
2
( c ) 2C2 H 2 ( g ) + 5O2 ( g ) → 4CO 2 ( g ) + 2H 2 O ( l ) ΔH rxn

= −2598.8 kJ / mol

2C ( graphite ) + H 2 ( g ) → C2 H 2 ( g )
Strategy
Our goal here is to calculate the enthalpy change for the formation of C 2H2
from its elements C and H2. The reaction does not occur directly, however,
so we must use an indirect route using the information given by Equations
(a), (b), and (c).
Solution
Looking at the synthesis of C2H2, we need 2 moles of graphite as reactant.
So we multiply Equation (a) by 2 to get
( d ) 2C ( graphite ) + 2O 2 ( g ) → 2CO 2 ( g ) ΔH rxn


= 2 ( −393.5 kJ / mol )
= −787.0 kJ / mol
Next, we need 1 mole of H2 as a reactant and this is provided by Equation
(b). Last, we need 1 mole C2H2 of as a product.
2C ( graphite ) + H 2 ( g ) → C2 H 2 ( g )
Equation (c) has 2 moles of C2H2 as a reactant so we need to

reverse the equation and divide it by 2:
5 1
(e) 2CO 2 ( g ) + H 2 O ( l ) → C 2 H 2 ( g ) + O 2 ( g ) ΔH rxn

= ( 2598.8 kJ / mol )
2 2
= 1299.4 kJ / mol
Adding Equations (d), (b), and (e) together, we get
2C ( graphite ) + 2O 2 ( g ) → 2CO 2 ( g ) 
1
H 2 ( g ) + O2 ( g ) → H 2 O ( l ) 
2
5
2CO 2 ( g ) + H 2 O ( l ) → C 2 H 2 ( g ) + O 2 ( g ) ΔH rxn

= 1299.4 kJ / mol
2
2C ( graphite ) + H 2 ( g ) → C 2 H 2 ( g ) 
ΔH rxn = 226.6 kJ / mol
Therefore,
ΔH f = 226.6 kJ / mol
This value means that when 1mole of C2H2 is

synthesized from 2 moles of C(graphite) and 1mole of
H2, 226.6 kJ of heat are absorbed by the reacting
system from the surroundings. Thus, this is an
endothermic process.

The thermite reaction involves

aluminum and iron(III) oxide
2Al ( s ) + Fe 2 O3 ( s ) → Al 2 O3 ( s ) + 2Fe ( l )
This reaction is highly exothermic

and the liquid iron formed is used
to weld metals.
Calculate the heat released in The molten iron formed in a

thermite reaction is run down into
a mold between the ends of two
railroad rails. On cooling, the rails
per gram of Al reacted with Fe 2 O3 . are welded together.
The ΔH f for Fe (l ) is 12.40 kJ / mol.

Strategy
The enthalpy of a reaction is the difference between
the sum of the enthalpies of the products and the sum
of the enthalpies of the reactants.
The enthalpy of each species (reactant or product) is

given by its stoichiometric coefficient times the
standard enthalpy of formation of the species.

2Al ( s ) + Fe2 O3 ( s ) → Al2 O3 ( s ) + 2Fe ( l )
Solution
Using the given ΔH f value for Fe(l) and other ΔH f
values in Appendix 3 and Equation (6.18), we write

ΔH rxn = ΔH f ( Al2 O3 )  + 2ΔH f ( Fe ) −  2ΔH f ( Al ) + ΔH f ( Fe 2 O3 ) 
= ( −1669.8 kJ / mol ) + 2 (12.40 kJ / mol )  −  2 ( 0 ) + ( −822.2 kJ / mol ) 
= −822.8 kJ / mol
This is the amount of heat released for

two moles of Al reacted. We use the
following ratio
−822.8 kJ
2 mol Al
to convert to kJ/g Al.
The molar mass of Al is 26.98 g, so
−822.8 kJ 1 mol Al
heat released per gram of Al = 
2 mol Al 26.98 g Al
= 15.25 kJ / g

End of Presentation
© McGraw-Hill Education. All rights reserved. Authorized only for instructor use in the classroom. No
reproduction or further distribution permitted without the prior written consent of McGraw-Hill Education. 6-98

Chang CH06 Thermochemistry

Uploaded by

Copyright:

Available Formats

Chang CH06 Thermochemistry

Uploaded by

Document Information

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Chang CH06 Thermochemistry

Uploaded by

Copyright:

Available Formats

CHM031 Lesson 4

• Compute the stoichiometric

• Compute heats of reaction from

• Compute the enthalpy of reaction

Energy is the capacity to do work.

© McGraw-Hill Education. 6-4

© 2019 McGraw-Hill Education. 6-11

• Heat is the transfer of thermal

Japanese research tells us what colours of clothing are6-12

• Heat is the transfer of thermal

Japanese research tells us what colours of clothing are6-13

The system is the specific part of the

5.2 Calorimetry – Chemistry (pressbooks.pub)

Jump to long description

Exothermic process is any process that gives off heat –

Endothermic process is any process in which

Jump to long description

First law of thermodynamics – energy can be converted

Chemical energy lost by Energy gained by the

© McGraw-Hill Education. 6-18

ΔU is the change in internal energy of a system

Table 6.1 Sign Conventions for Work and Heat

Work done by the system on the surroundings −

Work done on the system by the surroundings

Heat absorbed by the system from the surroundings

Heat absorbed by the surroundings from the system

© McGraw-Hill Education. 6-19

Jump to long description

A certain gas expands in volume from 2.0 L to 6.0 L at

Calculate the work done by the gas if it expands

(a) against a vacuum

(b) against a constant pressure of 1.2 atm

© McGraw-Hill Education. 6-21

The work done in gas expansion is equal to the product of the

What is the conversion factor between L · atm and J?

© McGraw-Hill Education. 6-23

To convert the answer to joules, we write

© McGraw-Hill Education. 6-24

The work done when a gas is compressed in a cylinder like

During this process, there is a heat transfer of 128 J from the

Calculate the energy change for this process.

© McGraw-Hill Education. 6-25

Heat is released by the gas to the surroundings.

Is this an endothermic or exothermic process?

What is the sign for q?

© McGraw-Hill Education. 6-26

As a result, the energy of the gas increases by 334 J.

© McGraw-Hill Education. 6-27

© McGraw-Hill Education. 6-28

Jump to long description

H products  H reactants H products  H reactants

System absorbs heat

System gives off heat

890.4 kJ are released for every 1 mole of methane that

Jump to long description

The stoichiometric coefficients always refer to the number

If you reverse a reaction, the sign of H changes.

If you multiply both sides of the equation by a factor n,

© McGraw-Hill Education. 6-33

The physical states of all reactants and products must