Determination of K, ΔG˚, ΔH˚, and ΔS˚

Slides:



Advertisements
Similar presentations
Entropy and Free Energy Chapter 19. Laws of Thermodynamics First Law – Energy is conserved in chemical processes neither created nor destroyed converted.
Advertisements

Chem. 31 – 2/23 Lecture. Announcements I Exam 1 –Next Monday (3/2) –Will Cover the parts we have covered in Ch. 1, 3 and 4 plus parts of Ch. 6 (through.
CAUSES OF CHANGE Order and Spontaneity. Enthalpy and Reactions Some reactions happen easily, but some others do not. Sodium and chlorine readily react.
Thermodynamics. Heat and Temperature Thermochemistry is the study of the transfers of energy as heat that accompany chemical reactions and physical changes.
By: Kyle Herd and Shannon Martin
Chemistry 312: Spring Review Endo v. Exo HW Endo v. Exo Pre Lab Questions Endo v. Exo Lab Notes on Specific Heat HW: Complete Lab Analysis Questions.
A spontaneous reaction (or favourable change) is a change that has a natural tendency to happen under certain conditions. Eg. The oxidation of iron (rust)
But more importantly is something called free energy G = H - TS want G to be negative, so that the free energy of the universe decreases, this is a spontaneous.
Thermo – the 2 nd Law Two factors effect any process such as a chemical reaction. 1.the difference in any energy term, ΔE, ΔH or ΔS, between the reactants.
Entropy and Free Energy. Free Energy and Spontaneous Reactions Many times, the energy (heat) released from a chemical reaction can be used to bring about.
Wednesday, Nov. 10 th : “A” Day Agenda  Section 10.4: Order and Spontaneity Entropy, Standard Entropy, Gibbs energy  Homework: Sec review, pg.
Catalyst Come in quietly and begin working on the Quiz that is on your desk End.
Causes of Change Order and Spontaneity Gibbs Energy and Predicting Spontaneity.
Equilibrium. Products can not escape reaction vessel Reaction becomes reversible Rate of forward equals rate of reverse Concentrations are constant.
Energy & Chemical Reactions. I.Kinetics – area of chemistry concerned with rates of chemical reactions A.Reaction Rates 1.The change of concentration.
The thermodynamics of the solubility of borax Determination of ΔH° and ΔS°
Section 18.4 Entropy. What you need to know - Entropy -Gibbs Free Energy -Enthalpy -Calculating Gibbs Free Energy -Determine if a rxn is spontaneous or.
Serial Dilutions Example!
Thermochemistry.  What is energy?  Energy is the ability to do work or produce heat.  The Law of Conservation of Energy: ◦ This law states that can.
Entropy and Free Energy. Before we begin… Do you have: Guided reading completed for sections 18.1 – 18.3 Section Review 18.3 Practice Problems completed.
CHAPTER 16: SPONTANEITY, ENTROPY, & FREE ENERGY Dr. Aimée Tomlinson Chem 1212.
The Scientific Method & Measurement. The Scientific Method Purpose Hypothesis Materials Procedure Observations Conclusions.
02/24/10 Lecture. Announcements Corrections to Monday’s Powerpoint Lecture Slides Posted (Slides 3, 9 and 15) I have posted last semester’s Exam 1 plus.
Thermodymanics.  Thermodynamics is a branch of science that focuses on energy changes that accompany chemical and physical changes.
The Driving Forces of Reactions. In chemistry we are concerned with whether a reaction will occur spontaneously, and under what conditions will it occur.
Entropy ( ) Entropy (S) is a measure of disorder in a system – Nature likes to create disorder (i.e., ΔS > 0) – Larger entropies mean that more energy.
Differential Scanning Calorimetry (4.6) Differential scanning calorimetry (DSC) is a way of measuring energy changes associated with physical transitions.

The Driving Forces of Reactions AP Chemistry. In chemistry we are concerned with whether a reaction will occur spontaneously, and under what conditions.
Energy Exchanges 1st Law of Thermodynamics 2nd Law of Thermodynamics
STANDARD HEAT OF FORMATION. DEFINITION The change in enthalpy that accompanies the formation of one mole of the compound at its normal state from its.
Making a Polymer. Rules!!! Hands should be clean to start Be sensible! Wash your hands afterwards!
 What is the formula for finding heat?  What are the two units of heat?  The temperature of a sample of iron with a mass of 10.0 g changed from 50.4.
Unit 11 Thermodynamics Chapter 16. Thermodynamics Definition Definition A study of heat transfer that accompanies chemical changes A study of heat transfer.
Chapter 17 Thermochemistry. Basics Thermochemistry Thermochemistry –Study of heat changes in a chemical reaction Calorimeter Calorimeter –Instrument used.
V. Determining Spontaneity It would be easier if we could determine spontaneity by just considering changes in the system. We derive an equation from the.
Entropy and Spontaneity Section 15.2 (AHL). Introduction Entropy can be regarded as a measure of the disorder or dispersal of energy in a system It measures.
Chapter 19 Part 4: Predicting reactions & the Third Law of Thermodynamics.
Thermodynamics By Alex Weber and Lee Cheung. Standard Thermodynamic Conditions 25 C°, and 1 barr = 100kPa ≈ 1 atm.
Prefixes in the Metric System
Free energy and Thermodynamics suroviec Spring 2014
Chapter 17 Thermochemistry. Basics Thermochemistry Thermochemistry –Study of heat changes in a chemical reaction Calorimeter Calorimeter –Instrument used.
Gibbs Free Energy Gibbs Free Energy The method used to determine spontaneity involves both ∆ S sys + ∆ S surr Gibbs deals with only the system,
Gibbs Free Energy. Gibbs Free Energy (G) Balances the relationship between enthalpy (ΔH) and entropy (ΔS) Balances the relationship between enthalpy (ΔH)
CHAPTER 19 SECTION 6 FREE ENERGY AND TEMPERATURE.
Question of the Day: 1. The value of ΔH° for the following reaction is -126 kJ. Determine the amount of heat (in kJ) that would be evolved by the reaction.
∆S and ∆H of fusion CHEMISTRY What are we going to do today?  Entropy ∆S  Melting Ice.  Use the thermistor to record the temperature  Use time.
Spontaneous process – any process, once started, proceeds without the external input of energy nonspontaneous process – any process which requires the.
Chapter 23 Thermodynamics What is the driving force for every process in the universe?
Heat Transfer and Change in Entropy – Gibbs Free Energy.
Chemistry 18.4.
To change any three variable equation
The thermodynamics of the solubility of borax
Reaction Energy and Reaction Kinetics
Aim # 18: What is the Gibbs Free Energy?
Enthalpy of Solution.
Reaction Rates.
AP Chemistry B Exam Prep Session Thermodynamics
Gibbs free energy and Cell energy
Chapter 17B Reaction Energy Entropy & Free Energy
Entropy and Free Energy
Gibbs Free Energy Main Concept:
Thermodynamics.
Entropy, Spontaneity, and Free Energy
GIBBS FREE ENERGY EQUATION
Gibbs Free Energy.
17-2 Driving Force of Reactions
Order and Spontaneity Entropy – a thermodynamic property is the measure of disorder in a system, the units are J/K and its symbol is S.
Chapter 19 Part 3: Free Energy.
Chapter 19 Part 3: Free Energy.
Presentation transcript:

Determination of K, ΔG˚, ΔH˚, and ΔS˚ Borax Na2B4O7·10H2O (Sodium Tetraborate Decahydrate ) Determination of K, ΔG˚, ΔH˚, and ΔS˚

Quiz Question # 4 Look at following equation to write down your Ksp:

First things first… Safety: Turn in Lab Reports LAB! Put bags away Goggles Lab Jacket Turn in Lab Reports LAB!

Borax Equilibrium

Let’s Simplify!!

Today’s Rxn

Gibbs Free Energy (ΔG), Enthalpy (ΔH), and Entropy (ΔS) = m x + b

Changes in Procedure Each group does one temp (assigned). 2 trials. Add 2 scoops of borax and 75 mL of distilled water to a beaker Heat the solution (<50 °C) so that the solution is saturated. Heat slowly! No need to speed up the heating process. Once slightly above assigned temperature, take off hotplate. If all the solid has dissolved, add some more borax to beaker. Pour 5 mL of the solution into a graduated cylinder once the solution is at the desired temperature. Record volume to tenths place. Be sure to record temperature to the tenths place.

Procedure (continued) Add the 5 mL of solution to an Erlenmeyer with 50 mL distilled water, 5 drops bromocresol green, mix thoroughly, add a little distilled water to rinse the graduated cylinder into the Erlenmeyer (Quantitative Transfer) Titrate with HCl (clean/rinse buret and fill w/ ~20 mL HCl) REPEAT! The above steps for two more titrations. DO NOT try to prepare three samples at once, unless you can guarantee the temperature of the borax solution will not change dramatically!

Volume Borax Solution Used Turn in class: Pre-lab, filled in data tables, observations Type in you and your partner’s data in class computers on opened excel spreadsheet Trial 1 Name [HCl] Temp Volume Borax Solution Used Volume HCl used   (M) (°C) (mL) Jack and Jill 0.250 33 5.2 5.9

Formal Lab Report – due in two weeks Table 1, 2 – for each trial solve for: Table 4 – average the trials to find (for each temp): Temp (K) mol HCl used mol borate ion [Borax] (M) Ksp lnKsp ΔG (kJ/mol) Temp (K) Ksp lnKsp ΔG (kJ/mol) 1/T

Data Tables (con’t) Table 5 – use ΔH and ΔS to solve for ΔG for each Temp Temp (K) ΔG (kJ/mol)

Graph: Make using Table 4 data

Calculations Find molarity of borax (mol/L) [Borax] Find Ksp Find moles borate (use moles HCl) Find volume of solution (borate + HCl) Find Ksp Ksp = 4[Borax]

Calculations Determine dH (kJ/mol) and dS (J/mol K) from this graph. note: dH = ΔH Use trendline from graph y = mx + b

Calculations con’t Calculate the values for dG for each sample using: dG = -RT ln Ksp used for table 4 dG = dH - TdS with your solved values for dH and dS used for table 5

Discussion Analysis Consider the following: Compare solving delta G between the two equations, which yielded better results? Consider the precision of the graphs