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Chapter 15 Thermochemistry
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Chapter 15

Dec 30, 2015

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Sarah Mason

Chapter 15. Thermochemistry. Energy. What is energy? Energy is the ability to do work or produce heat. The Law of Conservation of Energy: This law states that can not be created or destroyed only transferred. Two types of energy:. Heat. - PowerPoint PPT Presentation
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Page 1: Chapter 15

Chapter 15Thermochemistry

Page 2: Chapter 15

What is energy? Energy is the ability to do work or produce

heat. The Law of Conservation of Energy:

◦ This law states that can not be created or destroyed only transferred.

Two types of energy:

Energy

Page 3: Chapter 15

Heat is energy transferred from a warmer object to a cooler object.

Heat is represented mathematically as q.

Heat

Page 4: Chapter 15

A breakfast of cereal, orange juice, and milk contains 230 Calories. Convert this amount of energy in to Joules.

Problem

Page 5: Chapter 15

Glucose is a simple sugar found in fruit. Burning 1.00 g of glucose releases 15.6 kJ of energy. How many Calories are released?

3.73 Calories

An fruit and oatmeal bar contains 142 Calories. Convert this energy to Joules

5.94 x 105

A chemical reaction releases 86.5 kJ of heat. How many Calories are released?

20.7 Calories

Page 6: Chapter 15

The specific heat of any substance is the amount of heat required to raise the temperature of one gram of that substance by 1 degree Celsius.

Specific Heat

Page 7: Chapter 15

The specific heat of a substance can be used to calculate the heat energy absorbed or given off when that substance changes temperature.

Using Specific Heat

Page 8: Chapter 15

Thermochemistry is the study of heat changes during chemical reactions or phase changes.

When studying thermochemistry we look at two things:

System◦ The system is the specific part of the universe

that we are studying. Surroundings

◦ The surroundings are everything else in the universe.

Thermochemistry

Page 9: Chapter 15

Enthalpy is defined as the heat content of a system at constant pressure.

The change in enthalpy for a reaction is called the enthalpy (heat) of reaction.

ΔHrxn ΔHrxn = Hproducts – Hreactnats

Enthalpy and Enthalpy Change

Page 10: Chapter 15

A thermochemical equation is a balanced equation that includes the physical states of all reactants and products and the enthalpy change.

4 Fe(s) + 3 O2(g) 2 Fe2O3(s) ΔH = -1625 kJ

NH4NO3(s) NH4+(aq) + NO3

- ΔH = 27 kJ

Thermochemical Equations

Page 11: Chapter 15

Hess’s Law states that if you can add two or more equations to produce a final equation for a reaction than the sum of the enthalpy changes of the individual reactions is the enthalpy change of the overall reaction.

Hess’s Law

Page 12: Chapter 15

Calculate ΔH for the reaction 2 H2O2(l) 2 H2O(l) + O2(g)

2 H2(g) + O2(g) 2 H2O(l) ΔH = -572 kJ

H2(g) + O2(g) H2O2(l) ΔH = -188 kJ

Page 13: Chapter 15

Use equations (a) and (b) to determine ΔH for the following reaction:

2 CO(g) + 2 NO(g) 2 CO2(g) + N2(g)

a) 2 CO(g) + O2(g) 2 CO2(g) ΔH = -566.0 kJ

b) N2(g) + O2(g) 2NO(g) ΔH = -180.6 kJ

Page 14: Chapter 15

ΔH for the following reaction is -1789 kJ. Use equation (a) to determine ΔH for reaction (b).

4 Al(s) + 3 MnO2(s) 2 Al2O3(s) + 3 Mn(s)

a) 4 Al(s) + 3 O2 2 Al2O3(s) ΔH = -3352 kJ

b) Mn(s) + O2(g) MnO2 ΔH = ?

Page 15: Chapter 15

Formation Reaction:

S(s) + 3 F2(g) SF6 ΔHof = -1220 kJ

Sometimes we need to use fractional coefficients.

Enthalpy of Formation

Page 16: Chapter 15

We can use the enthalpy of formation for components of a reaction to calculate the total enthalpy change of the reaction (ΔHrxn).

H2S(g) + 4 F2(g) 2 HF(g) + SF6(g)

a) ½ H2(g) + ½ F2(g) HF ΔHof = -273 kJ

b) S(s) + 3 F2(g) SF6 ΔHof = -1220 kJ

c) H2(g) + S(s) H2S(g) ΔHof = -21 kJ

Using Enthalpy of Formation

Page 17: Chapter 15

Determine ΔH for CH4(g) + 2 O2(g) CO2(g) + 2 H2O(l)

Using: ΔHo

f(CO2) = -394 kJ ΔHo

f(H2O) = -286 kJ ΔHo

f(CH4) = -75 kJ ΔHo

f(O2) = 0 kJ

Page 18: Chapter 15

When things rust the reaction taking place is:

4 Fe(s) + 3 O2(g) 2 Fe2O3(s) ΔH = -1625 kJ

Any physical or chemical that occurs with no outside intervention is a spontaneous process.

Reaction Spontaneity

Page 19: Chapter 15

Entropy is a measure of the number of possible ways a system can be configured.

If we have a piece of paper cut into 8 different sections there would be 56 different ways we could arrange them. (8 x 7)

If we cut the paper into 16 different pieces there would be 240 different ways we could arrange them. (16 x 15)

We have increased the papers entropy.

Entropy

Page 20: Chapter 15

The second law of thermodynamics states that a spontaneous reaction will always occur in such a way that entropy increases.

Remember that the change in enthalpy (ΔH) is defined as:

Hproducts – Hreactants

Similarly: ΔS = Sproducts – Sreactants

If ΔS is positive the entropy of the system is increasing. If ΔS is negative the entropy of the system is

decreasing.

The Second Law Of Thermodynamics

Page 21: Chapter 15

• Phase Changes:◦ When a phase change occurs from a more

ordered state to a less ordered state ΔS will be positive.

◦ Solid Liquid ΔS > 0

◦ When a phase change occurs from a less ordered state to a more ordered state ΔS will be negative.

◦ Gas Liquid ΔS < 0• Dissolving a gas into a solvent always

results in a decrease in entropy.

Predicting Entropy Changes

Page 22: Chapter 15

Assuming no change in physical state, entropy increases when the number of moles of products is greater than the number of moles of reactants.◦ 2 SO3(g) 2 SO2(g) + O2(g)

Entropy increases when a solute dissolves in a solvent.◦ NaCl(s) Na+(aq) + Cl-(aq)

Entropy increases as temperature increases.

Page 23: Chapter 15

Predict the sign of ΔS for each of the following chemical of physical processes

ClF(g) + F2(g) ClF3(g) ΔS =

NH3(g) NH3(aq) ΔS =

Entropy has the units Joules/Kelvin

Page 24: Chapter 15

Named after physicist J. Willard Gibbs, free energy is the maximum amount of energy available during a chemical reaction.

Gibbs Free Energy Equation: ΔG = ΔH – TΔS

When a reaction occurs at standard conditions (298 K and 1atm)

ΔGo = ΔHo - ΔSo

Gibbs Free Energy

Page 25: Chapter 15

ΔG = ΔH – TΔS

A reaction where ΔH is negative and ΔS is positive will always be spontaneous.

N2(g) + 3 H2(g) 2 NH3(g) @ 298 K ΔH = -91.8 kJ ΔS = -197 J/k

ΔG = ΔG = -33.1 kJ

Page 26: Chapter 15

ΔH ΔS ΔG Reaction Spontaneity

ΔG = ΔH - TΔS

Page 27: Chapter 15

For a process ΔH is 145 kJ and ΔS is 322 J/K. Calculate ΔG for this reaction at 298 K. Is it spontaneous?