Energetics Topic 5.1 – 5.2.

Slides:



Advertisements
Similar presentations
Intro to Thermodynamics
Advertisements

International Baccalaureate Chemistry
Solid Liquid Gas MeltingVaporization Condensation Freezing.
IB Topics 5 & 15 PART 1: Heat and Calorimetry
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.
Chapter 51 Chapter 6 Thermochemistry Jozsef Devenyi Department of Chemistry, UTM.
Thermochemistry Chapter 6 AP Chemistry Seneca Valley SHS.
Thermochemistry.
Topic 5. Chemical Energetics
Energy and Heat. Definitions Thermochemistry: the study of the energy changes that accompany chemical reactions Energy: A property of matter describing.
ENTHALPY, HESS’ LAW, AND THERMOCHEMICAL EQUATIONS.
Energetics Topic 5.1 – 5.2 Topic 5.1 Exothermic and Endothermic Reactions.
Chapter 11 - Thermochemistry Heat and Chemical Change
Topic 5.1 Measuring Energy Changes total energy of the universe is a constant law of conservation of energy – if a system loses energy, it must be gained.
Energetics - IB Topics 5 & 15 adapted from Mrs. D. Dogancy. Above: thermit rxn PART 1 : HEAT AND CALORIMETRY.
Good Morning 11/16/2015 Today we will be working on the notes for ch 11.
Chemical Energetics Created by S. Colgan; Modified by K. Slater
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.
Industrial Applications of Chemical reactions
Chem10 Topic 01 - Thermochemistry Science 10 CT01D01.
Thermochemistry Some Like It Hot!!!!!. The Flow of Energy ► Thermochemistry – concerned with heat changes that occur during chemical reactions ► Energy.
3 Enthalpy. Units SI unit = joule 1KJ = 1000J = cal 1st law of Thermodynamics The total energy of the universe is constant i.e energy cannot be.
Topic 5.1 Measuring Energy Changes the conservation of energy is a fundamental principle of science – if a system loses energy, it must be gained by.
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.
Heat and Temperature 4. Heat is the TOTAL kinetic energy. 5. Temperature is the AVERAGE kinetic energy, measured by a thermometer.
IGCSE CHEMISTRY SECTION 4 LESSON 2. Content The iGCSE Chemistry course Section 1 Principles of Chemistry Section 2 Chemistry of the Elements Section 3.
Chemistry Unit 8 Thermochemistry Chapter The Flow of Energy Energy Transformations – Goal 1 Chemical Potential Energy Energy stored in chemical.
Topic 5.2 Calculations of enthalpy changes.  Specific heat (s) – the amount of heat necessary to raise the temperature of 1 g of a substance by 1 o C.
Thermodynamics The study of the changes of heat in chemical reactions.
Thermal Energy & Heat. Temperature Temperature  measure of the average KE of the particles in a sample of matter.
TO LIVE IS THE RAREST THING IN THE WORLD. MOST JUST EXIST. THAT IS ALL.
Topics 5 and 15. Hess’s Law Calorimetry Enthalpy Enthalpy of Formation Bond Energy.
Heat Transfer Reaction Energy Slides 1 Take out your homework.
5.2 Calorimetry and Enthalpy. Measuring Energy Changes Calorimetry is the experimental process used to measure the transfer of thermal energy. – A bomb.
Energetics. Enthalpy Change ∆H Chemical energy is a special form of potential energy that lies within chemical bonds. Chemical bonds are the forces of.
Chapter 10 Causes of Change
Unit 13 Thermochemistry.
Thermochemistry CHAPTER 17.
Exothermic and endothermic reactions Topic 5.1
Thermochemistry.
Chapter Ten Energy Changes in Chemical Reactions
THERMOCHEMISTRY.
Topic 5.2 Calculations of enthalpy changes
Chemical Energy and Calorimetry
Enthalpy Enthalpy is a measure of the total energy of a system.
Energy Changes and Rates of Reaction
Energy and Chemical Reactions
Thermochemistry Part 1 Chapter 17
IB Topics 5 & 15 PART 1: Heat and Calorimetry
Chemical Reaction Energy
Enthalpy and Calorimetry
Enthalpy, Entropy and Gibbs Law of Free Energy
Chapter 16 – Reaction Energy
Chapter 5 Notes: Energetics Thermochemistry
Heat in Reactions.
Energy Chapters 3,4,5,6.
Calorimetry and Enthalpy
It was a hot summer day. Mattie poured herself a glass of lemonade
Chapter 17 Thermochemistry
Energetics IB.
Thermochemistry.
Energy Changes.
Thermodynamics Lecture 1
Heat of Reaction & Enthalpy
IB Topics 5 & 15 PART 1: Heat and Calorimetry
PART 1: Heat and Calorimetry
Thermochemistry.
Enthalpy Most chemical and physical changes occur under essentially constant pressure (reactors open to the Earth’s atmosphere) very small amounts of work.
Presentation transcript:

Energetics Topic 5.1 – 5.2

Topic 5.1 Exothermic and Endothermic Reactions ? ?

total energy of the universe is a constant if a system loses energy, it must be gained by the surroundings, and vice versa

H Enthalpy a measure of the heat content (not temp) you cannot measure the actual enthalpy of a substance but you can measure an enthalpy CHANGE because of energy it takes in or releases  = Greek letter ‘delta’ meaning change H = heat. so, H means ‘heat change’.

Why a standard? enthalpy values vary according to the conditions a substance under these conditions is said to be in its standard state pressure: 100 kPa (1 atmosphere) temperature: usually 298K (25°C) if these were not standardized, then energy could be leaving or entering the system modify the symbol from Enthalpy Change Standard Enthalpy Change (at 298K)

Enthalpy (Heat) of Reaction H = Hproducts − Hreactants lower energy is more stable 6

Exothermic reactions heat energy is given out by the reaction hence the surroundings increase in temperature (feels hot) occurs when bonds are formed new products are more stable and extra energy is given off Hproducts < Hreactants H is negative examples combustion of fuels respiration neutralization reactions (acid reacts with something)

energy given out, ∆H is negative activation energy energy necessary to get the reaction going REACTION CO-ORDINATE ENTHALPY energy given out, ∆H is negative reactants products

H2 + Cl2  2HCl H, H, Cl, Cl (Atoms) H-H, Cl-Cl Reactants H-Cl, H-Cl Energy taken in to break bonds. H, H, Cl, Cl (Atoms) Energy given out when bonds are made. H-H, Cl-Cl energy Reactants Overall energy change, H H-Cl, H-Cl Products

H2 + Cl2  2HCl H, H, Cl, Cl (Atoms) H-H, Cl-Cl Reactants H-Cl, H-Cl Energy in = +678kJ H, H, Cl, Cl (Atoms) Energy out = -862kJ H-H, Cl-Cl energy Reactants Overall energy change, H = -184kJ H-Cl, H-Cl Products

Endothermic reactions heat energy is taken in by the reaction mixture hence the surroundings decrease in temperature (feels cold) occurs when bonds are broken the reactants were more stable (bonds are stronger) therefore, took energy from the surrounding to break bonds Hreactants < Hproduct H is positive examples

energy taken in, ∆H is positive activation energy energy necessary to get the reaction going REACTION CO-ORDINATE ENTHALPY energy taken in, ∆H is positive products reactants

14

Endothermic reactions Summary Table Exothermic reactions Endothermic reactions Energy is given out to the surroundings Energy is taken in from the surroundings ∆H is negative ∆H is positive Products have less energy than reactants Products have more energy than reactants

Topic 5.2 Calculation of enthalpy change Notice less sources of error here compared to our lab…

calorimetry calorimeter heat temperature measurement of heat flow device used to measure heat flow heat energy that is transferred from one object to another due to a difference in temperature measures total energy in a given substance temperature a measure of the average kinetic energy of a substance regardless how much is there

100ml of water contains twice the heat of 50 ml. Temperature vs. Heat 50 ml water 100 C 100 ml water 100C 100ml of water contains twice the heat of 50 ml.

Heat Capacity/Specific Heat the amount of energy a substance absorbs depends on: mass of material temperature kind of material and its ability to absorb or retain heat. heat capacity the amount of heat required to raise the temperature of a substance 1 oC (or 1 Kelvin) molar heat capacity the amount of heat required to raise the temperature of one mole 1 oC (or 1 Kelvin) specific heat the amount of heat required to raise the temperature of 1 gram of a substance 1 oC (or 1 Kelvin) 19

Specific Heat (c) values for Some Common Substances J g-1 K-1 Water (liquid) 4.184 Water (steam) 2.080 Water (ice) 2.050 Copper 0.385 Aluminum 0.897 Ethanol 2.44 Lead 0.127 or kJ kg-1 K-1 if multiply by 1000 20

Heat energy change q = m c DT q = change in heat (same as DH if pressure held constant) m = mass in grams or kilograms c = specific heat in J g-1 K-1 or kJ kg-1 K-1 (or Celsius which has same increments as Kelvin) DT = temperature change

Measuring the temperature change in a calorimetry experiment can be difficult since the system is losing heat to the surroundings even as it is generating heat. By plotting a graph of time vs. temperature it is possible to extrapolate back to what the maximum temperature would have been had the system not been losing heat to the surroundings.

Heat Transfer Problem 1 Calculate the heat that would be required to heat an aluminum cooking pan whose mass is 402.5 grams, from 20.5oC to 201.5oC. The specific heat of aluminum is 0.902 J g-1 oC-1. q = mcDT = (402.5 g) (0.902 J g-1 oC-1)(181.0oC) = 65,712.955 J = 65,710 J with correct sig. figs. only 4 sig. figs.

Heat Transfer Problem 2 Let T = final temperature What is the final temperature when 50.15 grams of water at 20.5oC is added to 80.65 grams water at 60.5oC? Assume that the loss of heat to the surroundings is negligible. The specific heat of water is 4.184 J g-1 oC-1 Solution: Dq (Cold) = Dq (hot) so… mCDT = mCDT Let T = final temperature (50.15 g) (4.184 J g-1 oC-1)(T- 20.5oC) = (80.65 g) (4.184 J g-1 oC-1)(60.5oC- T) (50.15 g)(T- 20.5oC) = (80.65 g)(60.5oC- T) 50.15T -1030 = 4880 – 80.65T 130.80T = 5830 T = 44.6 oC

Heat Transfer Problem 3 On complete combustion, 0.18g of hexane raised the temperature of 100.5g water from 22.5°C to 47.5°C. Calculate its enthalpy of combustion. Heat absorbed by the water… q = mcDT q = 100.5 (4.18) (25.0) = 10,500 J which is same as 10.5 kJ Moles of hexane burned = mass / molar mass = 0.18 g / 86 g/mol = 0.0021 moles of hexane Enthalpy change means find heat energy / mole = 10.5 kJ/ 0.0021 mol = 5000 kJ mol -1 or 5.0 x 103 kJ mol -1 hexane is C6H14