E. Calorimetry q = m C  T q = heat or enthalpy J m = mass g C = specific heat J/g°C  T = temperature change °C Note – these problems could also be done.

Slides:



Advertisements
Similar presentations
Intro to thermochem - Discuss HEAT v. TEMPERATURE
Advertisements

IB Topics 5 & 15 PART 1: Heat and Calorimetry
Thermochemistry Part 2: Calorimetry.
Thermodynamics.
Chapter 5 Thermochemistry
CHEMISTRY 161 Chapter 6
CDO Chemistry Thermodynamics 1 st Law of Thermodynamics 1 st Law – energy cannot be created or destroyed it can just change forms Energy can be.
EQ: Describe the parts and each part’s function in a calorimeter?
Calorimetry: :Measuring Heat
Enthalpy Changes Measuring and Expressing ∆H Calorimetry.
Chapter 51 Chapter 6 Thermochemistry Jozsef Devenyi Department of Chemistry, UTM.
Sections 5.4 – 5.6 Energy and Chemical Reactions.
Calorimetry & Enthalpy Changes
Thermodynamics Thermodynamics is the study of systems involving energy in the form of heat and work.
CHAPTER 17 THERMOCHEMISTRY.
THERMODYMANICS Thermodynamics is the study of the motion of heat energy as it is transferred from the system to the surrounding or from the surrounding.
Thermochemistry Chapter 5. First Law of Thermodynamics states that energy is conserved.Energy that is lost by a system must be gained by the surroundings.
CALCULATION OF ENTHALPY CHANGES. Molar Enthalpy  the enthalpy change for 1 mole of a substance associated with a chemical, physical or nuclear change.
Thermochemistry.
Thermodynamics: Energy Relationships in Chemistry The Nature of Energy What is force: What is work: A push or pull exerted on an object An act or series.
Enthalpy Enthalpy is a measure of the total energy of a system. Enthalpy is a state function (the pathway does not matter) with the symbol H. H = E + P.
1) vocab word--the quantity of heat needed to raise the temperature of 1 g of water 1°C 2) vocab word--the amount of energy required to raise the temperature.
Warm-up… EXPLAIN HOW THE ICE CREAM LAB WORKS
Enthalpy Changes Measuring and Expressing ∆H ☾ Calorimetry ☽
AP Chemistry Chapter 5 Jeopardy Jennie L. Borders.
Chapters 5 and 19.  Energy = capacity to do work  Kinetic = energy of motion  Potential = energy of position relative to other objects  Work = energy.
ENTHALPY, HESS’ LAW, AND THERMOCHEMICAL EQUATIONS.
Question of the Day: Day 4 2-8
Chapter 5: Thermochemistry. Thermochemistry: – Energy Kinetic & Potential – First Law of Thermo internal energy, heat & work endothermic & exothermic.
Calorimetry. Since we cannot know the exact enthalpy of the reactants and products, we measure  H through calorimetry, the measurement of heat flow.
CHM 108 SUROVIEC SPRING 2014 Chapter 6 Energy Transfer.
Energetics - IB Topics 5 & 15 adapted from Mrs. D. Dogancy. Above: thermit rxn PART 1 : HEAT AND CALORIMETRY.
CHAPTER 17 THERMOCHEMISTRY. ENERGY Energy is the capacity to do work or to supply heat. Various forms of energy include potential, kinetic, and heat.
Energy & Chemical Reactions Chapter 6. The Nature of Energy Chemical reactions involve energy changes Kinetic Energy - energy of motion macroscale - mechanical.
Thermochemistry. Do Now – Check and edit prelabs Objective – Thermochemistry Exothermic, endothermic, calorie, joule, heat capacity, and specific heat.
Thermochemistry. Energy Energy is the ability to do work or transfer heat. – Energy used to cause an object that has mass to move is called work. – Energy.
Thermodynamics 101Thermodynamics 101  First Law of Thermodynamics  Energy is conserved in a reaction (it cannot be created or destroyed)---sound familiar???
Chapter 15.4 & 15.5 ENTHALPY AND CALORIMETRY.  Thermochemistry = heat changes that accompany chemical reactions and phase changes  Energy released 
Chapter 6 – Energy. Types of Systems Energy First Law of thermodynamics: The energy of the universe is constant (i.e. energy is neither created nor destroyed)
Thermochemistry Chapter 6 (semester ) 6.1 The Narure of Energy and Types of Energy 6.2 Energy Changes in Chemical Recations 6.3 Introduction to Thermodynamics.
Calorimetry. Calculating Heat Q can be found experimentally by measuring the heat flow accompanying a reaction This is done by measuring temperature This.
Calorimetry. Calculating Heat Q can be found experimentally by measuring the heat flow accompanying a reaction This is done by measuring temperature This.
READING for Thursday: 7.3 – 7.4 READING for Thursday: 7.3 – 7.4 HOMEWORK – DUE TUESDAY 10/20/15 HOMEWORK – DUE TUESDAY 10/20/15 HW-BW 7.1 (Bookwork) CH.
Calorimetry Problems Chapter 6 part 3. Calorimetry Constant Pressure: measures enthalpy of rxn –coffee cup calorimetry Constant Volume: measures internal.
AgNO 3 + HCl  When 50.0 mL of M AgNO 3 and 50.0 mL of M HCl are mixed in a coffee-cup calorimeter, the mixture’s temperature increases from.
Enthalpy The Meaning of Enthalpy. 1. Enthalpy is a state function with the symbol H. H = E + PV E is the internal energy of the system, P is the pressure.
Calorimetry College Chemistry. 6. Specific Heat a. Some things heat up or cool down faster than others. Land heats up and cools down faster than water.
Exothermic  When heat is released (given off) by the system into the surroundings, the process is exothermic  H = H final − H initial  H = H products.
Thermochemistry pt 2. Calorimetry ΔH can be found experimentally or calculated from known enthalpy changes Measure heat flow with a calorimeter Heat capacity.
Calorimetry How is heat measured? It isn’t Temperature measured  T (K) C = heat capacity (J/K) = q (J) C = heat to raise T 1 o x.
Thermochemistry ENTHALPY. 1st Law of Thermodynamics  When a system absorbs energy, the surroundings release it  When a system releases energy, the surroundings.
Heat Transfer and Calorimetry Dr. Keith Baessler.
WARM UP 1.Given the thermochemical equation H 2 + I 2  2 HI, ΔH° rxn = 52 kJ/mol. What is ΔH° for the reaction HI  ½ H 2 + ½ I 2 ? 2.Given that the heat.
Thermal Energy & Heat. Temperature Temperature  measure of the average KE of the particles in a sample of matter.
HW 5.4 a. 200 KJ b. by 4 c. Heat up brakes and road a.  E = q + w b. No energy is not gained or lost. c. System loses heat or does work on the surroundings.
THERMODYNAMICS Courtesy of lab-initio.com Definitions #1 Energy: The capacity to do work or produce heat (sum of P.E. and K.E) Potential Energy: Energy.
6-1 Due: Nuclear Extra Credit Enthalpy Stoichiometry WS Today: 1. Intro to Calorimetry HW Connect Problems 6.3 Calorimetry Prep Lab Notebook: Investigating.
© 2009, Prentice-Hall, Inc. Work Usually in an open container the only work done is by a gas pushing on the surroundings (or by the surroundings pushing.
17.2 Measuring and Expressing Enthalpy Changes 1 > Copyright © Pearson Education, Inc., or its affiliates. All Rights Reserved. Chapter 17 Thermochemistry.
Heat capacity and Calorimetry
© 2012 Pearson Education, Inc.
Lecture 8: Thermochemistry
Chemical/physical changes in the lab are open to atmosphere, so the changes occur at a constant pressure Heat content of a system at constant pressure.
Thermochemistry Part 2: Calorimetry.
Chemical/physical changes in the lab are open to atmosphere, so the changes occur at a constant pressure Heat content of a system at constant pressure.
Lesson # 2: Enthalpy Calculations
A bag of chocolate candy has 220 Cal. How much energy is this in kJ?
THERMODYNAMICS Courtesy of lab-initio.com.
Measuring Enthalpy Changes
Calorimetry CP Unit 9 Chapter 17.
Presentation transcript:

E. Calorimetry q = m C  T q = heat or enthalpy J m = mass g C = specific heat J/g°C  T = temperature change °C Note – these problems could also be done in calories q sys = - q surr

Tells how much heat is required to change the temp of a substance. Some specific heats are Al0.902 J/g o C Cu0.385 J/g o C H 2 O4.184 J/g o C Quantity of heat supplied Temperature change (always Tf-Ti)

A 55.0 g piece of metal was heated in boiling water to a temperature of 99.8 o C and dropped into an insulated beaker with 225 mL of water (d = 1.00 g/ml) at 21.0 o C. The final temperature of the metal and water is 23.1 o C. Calculate the specific heat of the metal assuming that no heat was lost to the surroundings.

1. Pressure Constant (Coffee Cup) Calculate  H rxn in kJ/mol when mixing: 50 mL of 0.10M AgNO 3 50 mL of 0.10M HCl in a coffee cup calorimeter. The temperature rises from 22.3 °C to 23.1 °C. AgNO 3(aq) + HCl (aq)  AgCl (aq) + HNO 3(aq)

2. Volume Constant (Bomb Calorimeter) q rxn = - C bomb  T C bomb is an experimentally determined value using a known material. Each calorimeter has its own constant value!!

2. Volume Constant (Bomb Calorimeter) Octane, C 8 H 18, a primary constituent of gasoline, burns in air. 2 C 8 H 18(l) + 25 O 2(g)  16 CO 2(g) + 18 H 2 O (l) Suppose that a 1.00 g sample of octane is burned in a calorimeter that contains 1.20 kg of water. The temperature of the water and the bomb rises from o C to o C. If the specific heat of the bomb, C bomb, is known to be 837 J/ o C, calculate the molar heat of reaction of C 8 H 18.