Either way, you get to the finish.

Slides:



Advertisements
Similar presentations
1 Hesss Law Start Finish A State Function: Path independent. Both lines accomplished the same result, they went from start to finish. Net result = same.
Advertisements

Hess’s Law and Standard Enthalpies of Formation
Friday, Oct. 25 th : “A” Day Monday, Oct. 28 th : “B” Day Agenda  Homework questions/Quick review  Section 10.2 Quiz: “Using Enthalpy”  Section 10.3:
The basis for calculating enthalpies of reaction is known as Hess’s law: the overall enthalpy change in a reaction is equal to the sum of enthalpy changes.
1 Hess suggested that the sum of the enthalpies (ΔH) of the steps of a reaction will equal the enthalpy of the overall reaction. Hess’s Law.
 Certain reactions cannot be measured by calorimetry ◦ Ex: slow reactions, complex reactions, hazardous chemicals…  We can substitute in other reactions.
Learning Goals: Will be able to apply Hess’s Law to determine the enthalpy change of chemical equations. Will be able to write target equations from word.
16.1(b) Hess’s Law 1 2 POINT > Recall enthalpies of reaction, formation and combustion POINT > Define Hess’s Law POINT > Use Hess’s law to determine.
Thermochemistry Heat and Chemical Change
Chapter 2 The First Law Unit 4 thermochemistry
Hess’s Law 5.3 Energetics.
Hess’ Law energy changes are state functions. The amount of energy depends only on the states of the reactants and products, but not on the intermediate.
Section 4: Calculating Enthalpy Change
Calculating Enthalpy Change
Hess’s Law.
Industrial Chemistry Hess’s law.
Chapter 17: Thermochemistry
Enthalpy and Hess’s Law
AP CHEMISTRY NOTES Ch 6 Thermochemistry Ch 8.8 Covalent bond energies
Things are “heating up” now!
How much heat is released when 4
Hess’s Law Start Finish A State Function: Path independent.
Change in Enthalpy Unit 11.
Representing Energy Changes
|---> ∆Hvap ---> ---> ---> -->|
Hess’s Law and Standard Enthalpies of Formation
Formation Reactions Examples: C(s) + O2(g)  CO2(g)
Hess’s Law H is well known for many reactions, and it is inconvenient to measure H for every reaction in which we are interested. However, we can estimate.
Hess’s Law.
Unit 5: Thermochemistry
To Do 5th HW assignment due Friday by 10 pm.
Enthalpy of Reactions -We can describe the energy absorbed as heat at constant pressure by the change in enthalpy (ΔH) -the enthalpy of a reaction is the.
Stoichiometry Calculations involving Enthalpy
Enthalpy.
Heat in Chemical Reactions and Processes
Hess' Law Learning Goals:
Standard Enthalpy of Formation
Standard Enthalpies of Formation
List of enthalpies for several kinds of reactions.
Chapter 7: Thermochemistry
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.
Objectives - understand that chemical reactions involve the making and breaking of bonds and the concept of bond enthalpy  - be able to determine bond.
Energy and Chemical Reactions
Hess’s Law and Standard Enthalpies of Formation Unit 10 Lesson 4
AP Chem Get Heat HW stamped off Today: Enthalpy Cont., Hess’ Law
Rate of Chemical Reactions Unit 3 AOS 2
Hess’s Law and Standard Enthalpies of Formation Unit 10 Lesson 4
Chapter 16 Preview Objectives Thermochemistry Heat and Temperature
TOPIC 5 ENERGETICS/THERMOCHEMISTRY
Section 11.4 Calculating Heat Changes
Entropy & Chemical Reactions
Hess’s Law Hess’s law allows you to determine the energy of chemical reaction without directly measuring it. The enthalpy change of a chemical process.
Thermodynamics Heat of Formation.
THERMODYNAMICS #1 Example of using standard heats of formation to get ∆H of reaction Calculate the heat of reaction for the following combustion. 4 NH3.
THERMOCHEMISTRY Thermodynamics
Hess’s Law Start Finish A State Function: Path independent.
Hess’s Law Start Finish A State Function: Path independent.
Chapter 5 Thermochemistry Part B
Energy and Chemical Reactions
Hess’s Law Start Finish A State Function: Path independent.
1.2.5 Hess’s Law- the equation
Hess’s Law and Standard Enthalpies of Formation
Hess’s Law Start Finish A State Function: Path independent.
WebAssign #14 q=c∙m∙ΔT ΔHchange 693 kJ
Ch. 17: Reaction Energy and Reaction Kinetics
Thermodynamics.
Chapter 16 Thermochemistry
1.2.5 Hess’s Law- the equation
Chapter 16 Preview Objectives Thermochemistry Heat and Temperature
Changes in Enthalpy During Chemical Reactions
Presentation transcript:

Either way, you get to the finish. Hess’s Law The enthalpy change of a physical or chemical process is independent of the pathway of the process and the number of intermediate steps in the process. Finish Start Either way, you get to the finish.

Hess’s law allows you to determine the energy of chemical reaction without directly measuring it. The enthalpy change of a chemical process is equal to the sum of the enthalpy changes of all the individual steps that make up the process.

and.. the H values must be treated accordingly. Determine the heat of reaction for the reaction: 4NH3(g) + 5O2(g)  4NO(g) + 6H2O(g) Using the following sets of reactions: N2(g) + O2(g)  2NO(g) H = 180.6 kJ N2(g) + 3H2(g)  2NH3(g) H = -91.8 kJ 2H2(g) + O2(g)  2H2O(g) H = -483.7 kJ Hint: The three reactions must be algebraically manipulated to add up to the desired reaction. and.. the H values must be treated accordingly.

Found in more than one place, SKIP IT (its hard). Goal: 4NH3(g) + 5O2(g)  4NO(g) + 6H2O(g) Using the following sets of reactions: N2(g) + O2(g)  2NO(g) H = 180.6 kJ N2(g) + 3H2(g)  2NH3(g) H = -91.8 kJ 2H2(g) + O2(g)  2H2O(g) H = -483.7 kJ 4NH3  2N2 + 6H2 H = +183.6 kJ NH3: Reverse and x 2 Found in more than one place, SKIP IT (its hard). O2 : NO: x2 2N2 + 2O2  4NO H = 361.2 kJ H2O: x3 6H2 + 3O2  6H2O H = -1451.1 kJ

Found in more than one place, SKIP IT. Goal: 4NH3(g) + 5O2(g)  4NO(g) + 6H2O(g) 4NH3  2N2 + 6H2 H = +183.6 kJ NH3: Reverse and x2 Found in more than one place, SKIP IT. O2 : NO: x2 2N2 + 2O2  4NO H = 361.2 kJ H2O: x3 6H2 + 3O2  6H2O H = -1451.1 kJ Cancel terms and take sum. + 5O2 + 6H2O H = -906.3 kJ 4NH3  4NO Is the reaction endothermic or exothermic?

Consult your neighbor if necessary. Determine the heat of reaction for the reaction: C2H4(g) + H2(g)  C2H6(g) Use the following reactions: C2H4(g) + 3O2(g)  2CO2(g) + 2H2O(l) H = -1401 kJ C2H6(g) + 7/2O2(g)  2CO2(g) + 3H2O(l) H = -1550 kJ H2(g) + 1/2O2(g)  H2O(l) H = -286 kJ Consult your neighbor if necessary.

Determine the heat of reaction for the reaction: Goal: C2H4(g) + H2(g)  C2H6(g) H = ? Use the following reactions: C2H4(g) + 3O2(g)  2CO2(g) + 2H2O(l) H = -1401 kJ C2H6(g) + 7/2O2(g)  2CO2(g) + 3H2O(l) H = -1550 kJ H2(g) + 1/2O2(g)  H2O(l) H = -286 kJ C2H4(g) :use 1 as is C2H4(g) + 3O2(g)  2CO2(g) + 2H2O(l) H = -1401 kJ H2(g) :# 3 as is H2(g) + 1/2O2(g)  H2O(l) H = -286 kJ C2H6(g) : rev #2 2CO2(g) + 3H2O(l)  C2H6(g) + 7/2O2(g) H = +1550 kJ C2H4(g) + H2(g)  C2H6(g) H = -137 kJ

Homework: Page 317 #1-3

Where do the reference equations come from? Many can be determined through calorimetry. ie. combustion reactions Another type of reference equation is called standard enthalpies of formation.

Standard Enthalpies of formation: The standard enthalpy of formation is a measure of the energy released or consumed when one mole of a substance is created under standard conditions from its pure elements. The symbol of the standard enthalpy of formation is ΔHof. Δ = A change in enthalpy o = A degree signifies that it's a standard enthalpy change. f = The f indicates that the substance is formed from its elements An important point to be made about the standard enthalpy of formation is that when a pure element is in its standard form its standard enthalpy formation is zero.

ΔHoreaction=∑nΔHof(products)−∑nΔHof(Reactants) The equation for the standard enthalpy change of formation, shown below, is commonly used: ΔHoreaction=∑nΔHof(products)−∑nΔHof(Reactants) This equation essentially states that the standard enthalpy change of formation is equal to the sum of the standard enthalpies of formation of the products minus the sum of the standard enthalpies of formation of the reactants.

ΔHreactiono = ΔHfo[C] - (ΔHfo[A] + ΔHfo[B]) Given a simple chemical equation with the variables A, B and C representing different compounds: A+B⇋C and the standard enthalpy of formation values: ΔHfo[A] = 433 KJ/mol ΔHfo[B] = -256 KJ/mol ΔHfo[C] = 523 KJ/mol the equation for the standard enthalpy change of formation is as follows:  ΔHreactiono = ΔHfo[C] - (ΔHfo[A] + ΔHfo[B]) ΔHreactiono = (1 mol)(523 kJ/mol) - ((1 mol)(433 kJ/mol) + (1 mol)(-256 kJ/mol)) Because there is one mole each of A, B and C,  the standard enthalpy of formation of each reactant and product is multiplied by 1 mole, which eliminates the mol denominator: ΔHreactiono = 346 kJ The result is 346 kJ, which is the standard enthalpy change of formation for the creation of variable "C".

Calculate the ΔHreactiono for the formation of NO2(g). NO2(g) is formed from the combination of NO(g) and O2(g) in the following reaction: 2NO(g)+O2(g)⇋2NO2(g) To find the ΔHreactiono, use the formula for the standard enthalpy change of formation: ΔHoreaction=∑ΔHof(products)−∑ΔHof(Reactants) The relevant standard enthalpy of formation values from the data table are as follows: O2(g): 0 kJ/mol NO(g): 90.25 kJ/mol NO2(g): 33.18 kJ/mol Plugging these values into the formula above gives the following: ΔHreactiono= (2 mol)(33.18 kJ/mol) - ((2 mol)(90.25 kJ/mol) + (1 mol)(0 kJ/mol)) ΔHreactiono =-114.14kJ

Homework: Page 324 #1-6

Thermodynamic Quantities of Selected Substances @ 298.15 K