Hess' Law Learning Goals:

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

Enthalpy (H) The heat transferred sys ↔ surr during a chemical constant P Can’t measure H, only ΔH At constant P, ΔH = q = mCΔT, etc. Literally,
Hess’s Law: The algebraic addition of chemical equations yields a net equation whose enthalpy of reaction is the algebraic sum of the individual enthalpies.
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.
IIIIII Chapter 16 Hess’s Law. HESS’S LAW n If a series of reactions are added together, the enthalpy change for the net reaction will be the sum of the.
8.4 Thermochemical Equations Pages Thermochemical Equations A thermochemical equation is a balanced chemical equation that includes the physical.
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.
Example 17.1 Predicting the Sign of Entropy Change
Thermochemistry Heat and Chemical Change
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.
Calculating Heats of Reaction
Enthalpy and Hess’s Law
How much heat is released when 4
Hess’s Law Start Finish A State Function: Path independent.
In going from a particular set of reactants to a particular set of products, the change in enthalpy is the same whether the reaction takes place in one.
|---> ∆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.
Hess's Law.
Unit 5: Thermochemistry
DID YOU KNOW! Because of global warming, growing-season temperatures have increased by an average of 2°C (3.59°F) for most of the world's high-quality.
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’s Law The heat evolved or absorbed in a chemical process is the same whether the process takes place in 1 or several steps.
15.3 Thermochemical Equations
Chemistry Unit 13 Heat of Reaction.
Hess’s Law 17.4.
Objectives - understand that chemical reactions involve the making and breaking of bonds and the concept of bond enthalpy  - be able to determine bond.
Hess’s Law 17.4.
Not all chemical energy changes can be studied conveniently using simple calorimetry. Methods used to study these reactions are based on the principle.
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
Hess’s Law and Standard Enthalpies of Formation Unit 10 Lesson 4
DO NOW: On back of Notes! How much heat (in kJ) is given out when 85.0g of lead cools from 200.0C to 10.0C? (c=.129 J/gC)
Chapter 16 Preview Objectives Thermochemistry Heat and Temperature
Chapter 9 Chemical Quantities in Reactions
Hess's Law.
Section 11.4 Calculating Heat Changes
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.
Hess’s Law.
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
Either way, you get to the finish.
Energy and Chemical Reactions
Hess’s Law Start Finish A State Function: Path independent.
Thermochemistry Lesson # 4: Hess’s Law.
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
Intro to chemistry Therm o
Given this NET reaction
Warm-up: Hess’s Law and Calorimetry
1.2.5 Hess’s Law- the equation
5.4.6 Hess's Law of Heat Summation [1840]
Chapter 16 Preview Objectives Thermochemistry Heat and Temperature
Presentation transcript:

Hess' Law 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 equations

Hess’ Law Start Finish Path independent Both lines accomplished the same result, they went from start to finish. Net result = same.

Hess’s Law states…. The enthalpy change (ΔH) in a chemical reaction – from reactants to products – is the same whether the conversion occurs in one step or several steps. ie. ΔH is independent of the path taken

Hess’s Law Rules The value of the ΔH for any reaction can be written in steps equals the sum of the values of ΔH for each of the individual reactions. ∆Htarget = ∑ ∆Hunknowns If a chemical reaction is reversed then the sign of ΔH changes. If changes are made to the coefficients of a chemical equation (i.e. to balance it) then the value of ΔH is altered in the same way.

Example 1: What is the enthalpy change for the formation of nitrogen monoxide from its elements? N2(g) +O2(g) → NO(g) ΔH=? Given the following known reactions: ½N2(g) +O2(g) → NO2(g) ΔH= + 34kJ NO(g) + ½ O2(g) → NO2(g) ΔH= - 56kJ Hint: The three reactions must be algebraically manipulated to sum up to the desired reaction. and.. the H values must be treated accordingly.

Example 2: Find the ΔH for the reaction below, given the following reactions and subsequent ΔH values: 2CO2 (g) +H2O(g) →C2H2 (g) + 5/2 O2 (g) C2H2 (g) +2H2 (g) →C2H6 (g) ΔH=-94.5kJ H2O(g)  H2 (g) + ½ O2 (g) ΔH=71.2kJ C2H6 (g) +7/2O2 (g) →2CO2 (g) +3H2O(g) ΔH=-283kJ

Example 3: How much energy can be obtained from the roasting of 50.0kg of zinc sulphide ore? ZnS (s) + 3/2 O2 (g)  ZnO(s) + SO2(g) ZnO(s)  Zn(s) + ½ O2(g) ΔH= 350.5kJ S(s) + O2(g)  SO2(g) ΔH=-296.8kJ ZnS(s)  Zn(s) + S (s) ΔH= 206.0kJ

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: (1) N2(g) + O2(g)  2NO(g) H = 180.6 kJ (2) N2(g) + 3H2(g)  2NH3(g) H = -91.8 kJ (3) 2H2(g) + O2(g)  2H2O(g) H = -483.7 kJ 4NH3  2N2 + 6H2 H = +183.6 kJ NH3: (2)(Reverse and x 2) Found in more than one place, SKIP IT (its hard). O2 : NO: (1) (Same x2) 2N2 + 2O2  4NO H = 361.2 kJ H2O: (3)(Same 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 6H2 + 3O2  6H2O H = -1451.1 kJ H2O: x3 Cancel terms and take sum. H = 183.6 kJ + 361.2 kJ + (-1451kJ) + 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: TARGET  C2H4(g) + H2(g)  C2H6(g) H = ? Use the following reactions: (1) C2H4(g) + 3O2(g)  2CO2(g) + 2H2O(l) H = -1401 kJ (2) C2H6(g) + 7/2O2(g)  2CO2(g) + 3H2O(l) H = -1550 kJ (3) 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: (1) C2H4(g) + 3O2(g)  2CO2(g) + 2H2O(l) H = -1401 kJ (2) C2H6(g) + 7/2O2(g)  2CO2(g) + 3H2O(l) H = -1550 kJ (3) 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

Used for reactions that Summary: Used for reactions that cannot be determined experimentally Summary: H is independent of the path taken