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Transcript
Chapter 17 - Thermochemistry
-is the study of energy relationships
in chemical and physical reactions

almost nothing happens in chemistry
unless there is an energy advantage; all
reactions are an attempt to arrive at a
lower system energy.
a) 1st law of Thermodynamics: Law of
conservation of energy.
 Energy is never lost or gained , it only
changes form.
This law states that energy can change form
but is never really lost in any closed system.
b) 2nd law of Thermodynamics:
 Heat Energy always travels spontaneously
from a warmer body (body with higher
temperature) to a colder body.
-droping a hot rock in water
-frostbite
 OBJECTIVES:
• Explain the relationship between
energy and heat.
• Distinguish between heat capacity
and specific heat.
4
temperature is simply an indirect
measure of the average kinetic energy
of the particles in a sample of matter.
The scale of measurement is arbitrary:

i)
Celsius scale sets the zero
value at the freezing point of water at
101.325 kPa and 100 at the boiling point
of water at the same pressure.

ii) Kelvin scale sets the zero
value at absolute zero.
 The degrees are the same size as
celsius degrees.

Energy and Heat
 Thermochemistry
- concerned with
heat changes that occur during
chemical reactions
 Energy - capacity for doing work or
supplying heat
• weightless, odorless, tasteless
• if within the chemical substancescalled chemical potential energy
6
- represented by “q”, is energy
that transfers from one object to
another, because of a temperature
difference between them.
• only changes can be detected!
• flows from warmer  cooler object
 Heat
7
Exothermic and Endothermic
Processes
 Essentially
all chemical reactions,
and changes in physical state,
involve either:
• release of heat, (exothermic) or
• absorption of heat (endothermic)
 In
studying heat changes, think of
defining these two parts:
• the system - the part of the
universe on which you focus your
attention
• the surroundings - includes
everything else in the universe
 Together,
the system and it’s
surroundings constitute the
universe
 Thermochemistry is concerned with
the flow of heat from the system to
it’s surroundings, and vice-versa.
 The
Law of Conservation of Energy
states that in any chemical or
physical process, energy is neither
created nor destroyed.
• All the energy is accounted for as
work, stored energy, or heat.
flowing into a system from it’s
surroundings:
• defined as positive
• q has a positive value
• called endothermic
–system gains heat as the
surroundings cool down
 heat
flowing out of a system into it’s
surroundings:
• defined as negative
• q has a negative value
• called exothermic
–system loses heat as the
surroundings heat up
 heat
 Every
reaction has an energy
change associated with it
 Exothermic reactions release energy,
usually in the form of heat.
 Endothermic reactions absorb
energy
 Energy is stored in bonds between
atoms
14
Heat Capacity and Specific Heat
 A calorie
is defined as the quantity of
heat needed to raise the temperature
of 1 g of pure water 1 oC.
• Used except when referring to food
• a Calorie, written with a capital C,
always refers to the energy in food
• 1 Calorie = 1 kilocalorie = 1000 cal.
15
Heat Capacity and Specific Heat
 The
calorie is also related to the
joule, the SI unit of heat and energy
• named after James Prescott Joule
• 4.184 J = 1 cal
 Heat Capacity - the amount of heat
needed to increase the temperature
of an object exactly 1 oC
16
Heat Capacity and Specific Heat
 Specific
Heat Capacity - the
amount of heat it takes to raise the
temperature of 1 gram of the
substance by 1 oC often called
simply “Specific Heat”

mass; measured in g or kg. The greater
the mass, the more heat required to
change the temperature.
17
water, C = 4.18 J/(g oC),
 Thus, for water:
• it takes a long time to heat up, and
• it takes a long time to cool off!
 Water is used as a coolant!
 For
18
Heat Capacity and Specific Heat
 To
calculate, use the formula:
 q = m C T
 heat abbreviated as “q”
 m = mass
 T = change in temperature (Tf - Ti)
 C = Specific Heat
 Units are either J/(g oC) or kJ/(kg oC)
19
Table of Specific Heats
• Ex: Determine the heat required to
raise the temperature of 100g of water
from 298.0 K to 373.0 K .
Q = m c ΔT
Q = 100g (4.184 J/g K)( 373.0 K –
298.0 K)
Q = 418.4 J/K (75 K)
Q = 31350 J
Q = 31.4 kJ
21
22
Calorimetry
 Calorimetry
- the accurate and
precise measurement of heat
change for chemical and physical
processes.
 The device used to measure the
absorption or release of heat in
chemical or physical processes is
called a Calorimeter
Calorimetry
 Foam
cups are excellent heat
insulators, and are commonly used
as simple calorimeters
A Cheap
Calorimeter
 For
systems at constant pressure,
the heat content is the same as a
property called Enthalpy (H) of the
system
Calorimetry
in enthalpy = H
 q = H These terms will be used
interchangeably in this textbook
 Thus, q = H = m x C x T
 H is negative for an exothermic
reaction
 H is positive for an endothermic
reaction
 Changes
Calorimetry
 Calorimetry
experiments can be
performed at a constant volume
using a device called a “bomb
calorimeter” - a closed system
Energy
C + O2  CO2+ 395 kJ
C + O2
395kJ
C O2
Reactants

Products
30
In terms of bonds
C
O
O
O
C
O
Breaking this bond will require energy.
O
C
O C O
O
Making these bonds gives you energy.
In this case making the bonds gives you
more energy than breaking them.
31
Exothermic
 The
products are lower in energy
than the reactants
 Releases energy
32
Energy
CaCO
 CaO
CaCO
CaO
+ CO+2 CO2
3 + 176
3 kJ
CaO + CO2
176 kJ
CaCO3
Reactants

Products
33
Endothermic
 The
products are higher in energy
than the reactants
 Absorbs energy
34
Chemistry Happens in
MOLES
An equation that includes energy is
called a thermochemical equation
 CH4 + 2O2  CO2 + 2H2O + 802.2 kJ
 1 mole of CH4 releases 802.2 kJ of
energy.
 When you make 802.2 kJ you also
make 2 moles of water

35
What is the molar enthalpy of CO2 (g) in the
reaction for the burning of butane below?
2 C4H10 +13 O2  8 CO2 +10 H2O
∆H=-5315 kJ
Answer:
Molar enthalpy is the enthalpy change in
equation divided by the balance of CO2
 Molar enthalpy, H substance = 5315 kJ ÷ 8
mol

= 664 kJ / mol.

Thermochemical Equations
 A heat
of reaction is the heat
change for the equation, exactly
as written
• The physical state of reactants
and products must also be given.
• Standard conditions for the
reaction is 101.3 kPa (1 atm.)
and 25 oC
37
CH4 + 2 O2  CO2 + 2 H2O + 802.2 kJ

If 10. 3 grams of CH4 are burned
completely, how much heat will be
produced?
10. 3 g CH4
1 mol CH4
16.05 g CH4
802.2 kJ
1 mol CH4
= 514 kJ
38
CH4 + 2 O2  CO2 + 2 H2O + 802.2 kJ
 How
many liters of O2 at STP would
be required to produce 23 kJ of
heat?
 How many grams of water would be
produced with 506 kJ of heat?
39

How much heat will be released if 65 grams of butane
is burned in a lighter according the equation:
2 C4H10 +13 O2  8 CO2 +10 H2O
∆H=-5315 kJ
 1molC4 H10  5315kJ 

65 gC4 H10 

 58.14 g  2molC4 H10 
= 2976.4 kJ
= 3.0 MJ
Calculate the heat released when 120 grams
of Iron (III) oxide is formed by the following
equation
2 Fe2O3 (s) → 4 Fe(s)+3 O2 (g)
∆H=1625 kJ

 1molFe2O3  1625kJ 
120 gFe2O3 


 159.70 g  2mol 
= 610.5 kJ
= 610 kJ

Q = n ∆H (substance)
Where n = # of moles
What mass of carbon dioxide must form
to create 1200 kJ of heat when the
following reaction occurs?
C6H12O6(s)+6O2(g)→6CO2(g)+6H2O(l)
∆H=- 2808kJ
Answer: 110 grams

3) What mass of oxygen is needed to
completely react and release 550 kJ of
heat in the following reaction?
 4Fe (s)+3O2 (g) → 2 Fe2O3 (s)

∆H=- 1625 kJ
Answer: 32 grams
Summary, so far...
Enthalpy
 The
heat content a substance has at a
given temperature and pressure
 Can’t be measured directly because
there is no set starting point
 The reactants start with a heat content
 The products end up with a heat
content
 So we can measure how much
enthalpy changes
46
Enthalpy
 Symbol
is H
 Change in enthalpy is H (delta H)
 If heat is released, the heat content of
the products is lower
H is negative (exothermic)
 If heat is absorbed, the heat content
of the products is higher
H is positive (endothermic)
47
Energy
Change is down
H is <0
Reactants

Products
48
Energy
Change is up
H is > 0
Reactants

Products
49
Heat of Reaction
The heat that is released or absorbed in a
chemical reaction
 Equivalent to H
 C + O2(g)  CO2(g) + 393.5 kJ
 C + O2(g)  CO2(g)
H = -393.5 kJ
 In thermochemical equation, it is important
to indicate the physical state
 H2(g) + 1/2O2 (g) H2O(g) H = -241.8 kJ
 H2(g) + 1/2O2 (g) H2O(l) H = -285.8 kJ

50
Heat of Combustion
 The
heat from the reaction that
completely burns 1 mole of a
substance
51
 OBJECTIVES:
• Classify, by type, the heat changes
that occur during melting, freezing,
boiling, and condensing.
52
 OBJECTIVES:
• Calculate heat changes that occur
during melting, freezing, boiling,
and condensing.
53
Heats of Fusion and
Solidification
 Molar
Heat of Fusion (Hfus) - the
heat absorbed by one mole of a
substance in melting from a solid to
a liquid
 Molar Heat of Solidification (Hsolid)
- heat lost when one mole of liquid
solidifies
54
Heats of Fusion and
Solidification
 Heat
absorbed by a melting solid is
equal to heat lost when a liquid
solidifies
• Thus, Hfus = -Hsolid
55
Heats of Vaporization and
Condensation
 When
liquids absorb heat at their
boiling points, they become vapors.
 Molar Heat of Vaporization (Hvap) the amount of heat necessary to
vaporize one mole of a given liquid.
56
Heats of Vaporization and
Condensation
 Condensation
is the opposite of
vaporization.
 Molar Heat of Condensation (Hcond)
- amount of heat released when one
mole of vapor condenses
 Hvap = - Hcond
57
Heats of Vaporization and
Condensation
The large values for Hvap and Hcond
are the reason hot vapors such as
steam is very dangerous
• You can receive a scalding burn
from steam when the heat of
condensation is released!
58
Heats of Vaporization and
Condensation
 H20(g)
 H20(l)
Hcond = - 40.7kJ/mol
59
Heat of Solution
 Heat
changes can also occur when
a solute dissolves in a solvent.
 Molar Heat of Solution (Hsoln) heat change caused by dissolution
of one mole of substance
 Sodium hydroxide provides a good
example of an exothermic molar
heat of solution:
60
Heat of Solution
NaOH(s)
H2O(l)

Na1+(aq) + OH1-(aq)
Hsoln = - 445.1 kJ/mol
 The heat is released as the ions
separate and interact with water,
releasing 445.1 kJ of heat as Hsoln
thus becoming so hot it steams
61
 OBJECTIVES:
• Apply Hess’s law of heat
summation to find heat changes
for chemical and physical
processes.
62
 OBJECTIVES:
• Calculate heat changes using
standard heats of formation.
63
Hess’s Law
 If
you add two or more
thermochemical equations to give a
final equation, then you can also
add the heats of reaction to give
the final heat of reaction.
Called Hess’s law of heat summation
64
Why Does It Work?
If you turn an equation around, you change
the sign:
 If H2(g) + 1/2 O2(g) H2O(g) H=-285.5 kJ
 then,
H2O(g) H2(g) + 1/2 O2(g) H =+285.5 kJ
 also,
 If you multiply the equation by a number,
you multiply the heat by that number:
 2 H2O(g) H2(g) + O2(g) H =+571.0 kJ

65
You make the products, so you need
their heats of formation
 You “unmake” the products so you have
to subtract their heats.
 How do you get good at this?

66
Standard Heats of Formation
The H for a reaction that produces 1
mol of a compound from its elements at
standard conditions
 Standard conditions: 25°C and 1 atm.
0
 Symbol is H
f

The
standard heat of formation of an
element = 0
This
includes the diatomics
67
What good are they?
Table 11.6, page 316 has standard
heats of formation
 The heat of a reaction can be calculated
by:
• subtracting the heats of formation of
the reactants from the products

Ho = (H 0f Products) - (H 0f Reactants)
68
Examples

CH4(g) + 2 O2(g)  CO2(g) + 2 H2O(g)
0
H f CH4 (g) = - 74.86 kJ/mol
0
H f O2(g) = 0 kJ/mol
0
H f CO2(g) = - 393.5 kJ/mol
0
H f H2O(g) = - 241.8 kJ/mol

H= [-393.5 + 2(-241.8)] - [-74.68 +2 (0)]
H= - 802.4 kJ
69
Examples
70