CHEMISTRY 135. Kinetics: Iodination of Acetone

Similar documents
CHEMISTRY 135 General Chemistry II. Determination of an Equilibrium Constant

So, What Does it Indicate?

Thermochemistry. Introduction. Pre-lab. Safety

aa + bb cc + dd Equation 1

CHEMISTRY 130 General Chemistry I. Thermochemistry

Kinetics of Crystal Violet Fading AP Chemistry Big Idea 4, Investigation 11 An Advanced Inquiry Lab (adapted by Flinn Scientific, Inc.

REACTIONS THAT OSCILLATE

So, What Does it Indicate?

Kinetics of Crystal Violet Fading AP* Chemistry Big Idea 4, Investigation 11 An Advanced Inquiry Lab

Determining the Rate Law for a Chemical Reaction

Chemistry 213. A KINETIC STUDY: REACTION OF CRYSTAL VIOLET WITH NaOH LEARNING OBJECTIVES

CHEMISTRY 130 General Chemistry I OXIDATION-REDUCTION CHEMISTRY

CHEMISTRY 130 General Chemistry I OXIDATION-REDUCTION CHEMISTRY

Lab- Properties of Acids and Bases. Name. PSI Chemistry

C H E M I S T R Y DETERMINATION OF AN EQUILIBRIUM CONSTANT

Experiment 13H THE REACTION OF RED FOOD COLOR WITH BLEACH 1

Introduction. Concepts Kinetics Order of reaction Reaction rate Colorimetry. Background

THE IRON(III) THIOCYANATE REACTION SYSTEM

CH 112 Special Assignment #4 Chemistry to Dye for: Part C

Determining the Rate Law and Activation Energy for the Methyl Blue Reaction:

Learn to do quantitative titration reactions. Observe the mole ratios of several simple chemical reactions.

1-50 ml beaker stirring rod 1-10 ml beaker 0.10 M NaOH (1 ml) calibrated plastic dropper (1 ml) 50 ml dispensing burette (for Crystal Violet)

Lab Investigation 4 - How Fast Does the Crystal Violet Decolorize?

Rate law Determination of the Crystal Violet Reaction Using the Isolation Method

CHEMISTRY 130 General Chemistry I. Acetic Acid in Vinegar

Experiment 10 Chemical Kinetics Discovery Lab. Last week in lab. Thermo vs Kinetics. CH 204 Fall 2009 Dr. Brian Anderson

PURPOSE: To determine the Rate Law for the following chemical reaction:

Chemistry CP Lab: Additivity of Heats of Reaction (Hess Law)

CHEMISTRY 135 General Chemistry II. Energy of Phase Changes [1]

Titration with an Acid and a Base

Pre-lab: Read sections 10.6 in the textbook. Complete the attached pre-lab by Thursday, May 22.

RATE LAW DETERMINATION OF CRYSTAL VIOLET HYDROXYLATION

Experiment 7. Determining the Rate Law and Activation Energy for the Reaction of Crystal Violet with Hydroxide Ion

GETTING THE END POINT TO APPROXIMATE. Two hours

Experiment 13I THE REACTION OF RED FOOD COLOR WITH BLEACH 1

Classifying Chemical Reactions: Lab Directions

RATE LAW DETERMINATION OF CRYSTAL VIOLET HYDROXYLATION

A Chemical Clock. 5. Consider each of the following questions regarding data and measurements:

Skill Building Activity 2 Determining the Concentration of a Species using a Vernier Spectrometer

EXPERIMENT 8 Determining K sp

Experiment 1 Chemical Kinetics 1

The Kinetics of the Iodine Clock Reaction

Chem 2115 Experiment #7. Volumetric Analysis & Consumer Chemistry Standardization of an unknown solution, analysis of vinegar & antacid tablets

The periodic table is the most recognized symbol in chemistry across the world. It is a valuable tool that allows scientists not only to classify the

Chemical Kinetics: Determining Rate Laws for Chemical Reactions

The Energy of Phase Changes

Pre-lab: Read section 9.9 (pages ) on acid-base titrations in the textbook. Complete the attached pre-lab by Tuesday, June 2.

Determination of an Equilibrium Constant

Experiment 20-Acid-Base Titration: Standardization of KOH and Determination of the Molarity and/or Percent Composition of an Acid Solution

Rate of Reaction. Introduction

Bellevue College CHEM& 121 Experiment: Stoichiometric Analysis of an Antacid 1

Analysis of Hypochlorite in Bleach

Just a reminder that everything you do related to lab should be entered directly into your lab notebook. Calorimetry

Exp 03 - Reaction Rate

ENTHALPY OF FORMATION OF MgO

Introduction to Spectroscopy: Analysis of Copper Ore

Experiment 7: SIMULTANEOUS EQUILIBRIA

Acidity of Beverages Lab

Determination of an Equilibrium Constant

Acids and Bases. How does ph affect biological solutions? Introduction. Prelab Preparation Review Section 2.3 on acids and bases in your textbook.

Experiment#1 Beer s Law: Absorption Spectroscopy of Cobalt(II)

Experiment #7. Determination of an Equilibrium Constant

Experiment 18 - Absorption Spectroscopy and Beer s Law: Analysis of Cu 2+

IODINE CLOCK REACTION KINETICS

Acid Base Titration Experiment ACID - BASE TITRATION LAB

Experiment 7 Can You Slow It Down?

Acid-Base Titration Acetic Acid Content of Vinegar

Chem 2115 Experiment #7. Volumetric Analysis & Consumer Chemistry Standardization of an unknown solution and the analysis of antacid tablets

Developing a Spectrophotometric Quantitative Assay for p-nitrophenol

UW Department of Chemistry Lab Lectures Online

Lab #12: Determination of a Chemical Equilibrium Constant

Lab #5 - Limiting Reagent

Micro Mole Rockets. Hydrogen and Oxygen Mole Ratio

Energy. Position, x 0 L. Spectroscopy and the Particle-in-a-Box. Introduction

KINETICS OF THE PERMANGANATE- ISOPROPYL ALCOHOL REACTION

Iodine Clock Challenge Rate Laws

KINETICS: INITIAL RATES

Introduction. Objectives

CHEMICAL KINETICS E + 2B 2C + D (1)

To determine relative oxidizing and reducing strengths of a series of metals and ions.

Determination of an Equilibrium Constant Minneapolis Community and Technical College Principles of Chemistry II, C1152 v.1.16

Introduction to Spectroscopy: Analysis of Copper Ore

, but bursts into flames in pure oxygen.

Chesapeake Campus Chemistry 111 Laboratory

Absorption Spectra of Cyanine Dyes

Lab Report Rate of Chemical Reaction: The Iodination of Acetone

Name Period Date. Lab 9: Analysis of Commercial Bleach

Lab Activity 3: Factors Affecting Reaction Rate

When a solution of thiosulfate is acidified, the following reaction takes place: S2O3 2 - (aq) + 2H + (aq) H2O + SO2 (g) + S (s) (1)

CHM112 Lab Determination of an Equilibrium Constant Grading Rubric

Determination of an Equilibrium Constant Minneapolis Community and Technical College Principles of Chemistry II, C1152 v.9.13

GENERAL INSTRUCTIONS

Safety Note: Safety glasses and laboratory coats are required when performing this experiment

DETERMINATION OF AN EQUILIBRIUM CONSTANT

Properties of Acids and Bases

EXPERIMENT 6 Empirical Formula of a Compound

Aspirin Lab By Maya Parks Partner: Ben Seufert 6/5/15, 6/8/15

THE LAWS LAB LAW OF CONSERVATION OF MASS, LAW OF DEFINITE PROPORTIONS, LAW OF MULTIPLE PROPORTIONS

EXPERIMENT 5 ACID-BASE TITRATION

A Clock Reaction: Determination of the Rate Law for a Reaction

Transcription:

CHEMISTRY 135 General Chemistry II Kinetics: Iodination of Acetone Pearson Education Conceptually, reaction rates are determined by counting reactant and product molecules at designated times. How might we assess the concentrations of reactants or products in a real laboratory experiment? Can we design an experiment to determine the rate law? DEPARTMENT OF CHEMISTRY UNIVERSITY OF KANSAS

Introduction Kinetics: Iodination of Acetone An important feature of a chemical reaction is its rate. Here, the term rate describes how quickly (or how slowly) a chemical reaction proceeds. For example, decomposition of hydrogen peroxide solution, H 2 O 2, occurs quite slowly if contained in a bottle in a home medicine cabinet. 2H 2 O 2 2H 2 O + O 2 However, in the presence of a catalyst--a substance that speeds the rate of a chemical reaction--hydrogen peroxide decomposes more quickly. The point is that this chemical equation, like any chemical equation, describes a chemical reaction. However, it tells us nothing about the rate. The field of chemistry that explores rates is called chemical kinetics. In this particular lab, you will gain firsthand experience acquiring kinetic data: you will measure the amount of time it takes for a chemical reaction to occur, and use that information to calculate the overall rate of that reaction. The system you will study is the reaction of iodine with acetone. This is a convenient chemical reaction for us to study because I 2 is a colored species, observable with the eye or with spectrophotometers like ours. A catalyst will be used to ensure that the reaction proceeds fairly quickly. The catalyst is the strong acid HCl, which we will simply abbreviate H +. The H + is written directly above the reaction arrow, as it is not a reactant, per se, but it is an important participant. H + CH 3 COCH 3 + I 2 CH 3 COCH 2 I + I - + H + acetone All chemical reactions have an associated rate law. For example, the rate law for the iodination of acetone has the following form: rate = k [acetone] x [H + ] y The rate law describes how the concentrations (shown in square brackets) of the participants in the chemical reaction impact the rate. Thus [acetone] and [H + ] refer to the concentrations of acetone and H +, respectively. k is a constant of proportionality, known as the rate constant, which is characteristic of the specific reaction and the system temperature. Rate itself, on the left hand side of the equation above, is a term that refers to the rate of disappearance (or the rate of appearance, depending on the species of interest) of a given reactant or product; it is measured in units of concentration/time. (We ll generally use M/s or M/min.) The ultimate goal for today s lab is to determine the values for x and y the exponents in the rate law. As you can see, these exponents provide a critical mathematical link between concentrations and the overall reaction rate. Using the reaction and conditions described here, you can assume that both x and y are equal to some small whole number. Furthermore, you can assume that the concentration of I 2, the colored reactant, will not impact the rate. (Did you notice that [I 2 ] does not appear anywhere in the rate law given above for the reaction?)

Given these assumptions, it will be possible for you and your group members to conduct a series of simple experiments to determine not only x and y but also k, the rate constant for the iodination of acetone at the lab room temperature. How can we determine so many different values using just one experiment? The answer is that we will do a series of closely related experiments, taking advantage of the variety of concentrations of reaction participants available to you. Specifically, you will vary the concentration of acetone in some experiments, and you will vary the concentration of HCl (that is, [H + ]), in others. In each of these individual trials, your goal will be to assess the rate at which I 2 disappears. Since rate involves both concentration and time, the two pieces of raw data needed, at minimum, are the starting concentration of I 2, along with the amount of time required for it to disappear. We ll call the reaction starting time t 0 and we ll refer to the ending time (that is, when all of the I 2 is gone and the solution has turned colorless) simply as t. Pre-lab Safety: You must wear goggles, as you always do in the laboratory. Iodine is toxic and stains skin and clothing. Note: A small skin stain is not dangerous. Iodine solutions were once used to treat minor cuts. Acetone is highly flammable. There should be absolutely no open flames in the laboratory. Acetone and acetone solution bottles should be closed when not in use. Hydrochloric Acid and other acids are hazardous if splashed on clothing, exposed skin or in the eyes. Prolonged exposure of the skin to even fairly dilute solutions of acid can cause burns. If acids and bases splash on skin or clothes, remove the affected clothing and flush the affected areas thoroughly with cold water. Prior to considering this week's prelab questions, please read this lab write-up in its entirety, and read sections 14.1 through 14.4 of your Tro Chemistry textbook. You may find it helpful to bring your Chemistry textbook to lab. 1. List all of the chemicals you will use for this week's experiment. For each chemical, list specific safety precaution(s) that must be followed. In order to find specific safety information, please obtain a Materials Safety Data Sheet (MSDS) on the chemical of interest. MSDSs can be found through an internet search (e.g., google) or from the following website: www.hazard.com. Read the MSDS and find specific safety concerns for each chemical. List the chemicals you will use for the hands-on portion of this week's lab experiment. For each chemical, list specific safety precaution(s) that must be followed. 2. What is the chemical equation for the reaction we will study in this week s experiment? 3. Define the word catalyst. What substance will be used as a catalyst in this week s experiment? 4. Write the rate law for the general reaction given by aa + bb cc + dd 5. Determine the rate of the chemical reaction 2NO + 2H 2 N 2 + 2H 2 O, given an NO concentration of 12.0 x 10-3 M, an H 2 concentration of 3.0 x 10-3 M, and a rate constant k of 2.5 x 10 2 M -2 s -1 The rate law for this reaction is rate = k [NO] 2 [H 2 ]

Procedure Preparation of Solutions and Spectrometer 1. Be sure to turn on the spectrometer and, after a brief warm-up, calibrate it. 2. Prepare an acetone solution by placing 10.0 ml of pure acetone in a 50-mL size volumetric flask, and diluting to the mark with distilled water. What is the molar concentration of this solution? First Timed Trial The following is a suggested procedure for the very first timed trial(s) you perform for the iodination of acetone. (Once you are convinced that your group can execute this procedure reproducibly, you ll be ready to use the guidelines entitled Studying the Impact of Acetone and H + Concentrations to plan subsequent runs.) 1. Place 1.9 ml of distilled water in a cuvette 2. Add 0.8 ml of 1.0 M HCl 3. Add 0.8 ml of your group s prepared acetone solution 4. Ready your stopwatch/clock to time your reaction 5. Add 0.5 ml of 0.005 M I 2 solution 6. Begin timing the reaction immediately; place a cap on the cuvette and invert the cuvette several times to mix the contents 7. Place the cuvette in the calibrated spectrophotometer. Monitor the absorbance at 400 nm; record these readings at regular intervals until the absorbance reaches a nominal zero value (i.e., negligible absorbance). Studying the Impact of Acetone and H + Concentrations As you plan for subsequent timed trials that is, the ones in which the concentrations of acetone and acid are varied, with the aim of determining the exponents, x and y, in the rate law there are several experimental constraints that must be borne in mind. First, our spectrometer, like any spectrometer, has a limited working range for absorbance measurements. As such, it is recommended that you not adjust the concentration of I 2 from one trial to the next. Instead, add 0.5 ml of 0.005 M I 2 for every trial. (This is not a practical inconvenience, since we have already stated that [I 2 ] does not impact the rate of the chemical reaction under the conditions selected.) The second experimental limitation is that the reagent solutions are limited to your prepared acetone solution and the provided stock solutions. As such, your group will have to adjust the volume of a given reagent added to a cuvette if you wish to vary its concentration. This approach works well because each cuvette holds 4.0 ml of liquid; any increase or decrease in the quantity of acetone or HCl added should be accompanied by a corresponding change in the volume of added water, so that a net volume of 4.0 ml is employed for every trial. (This is also a practical concern; the spectrometer is not designed for use with partially filled cuvettes.) For example, if your group wanted to double the concentration of acetone relative to the starting recipe given above, the following combination of reagents would be recommended: 1.1 ml distilled water 1.6 ml acetone solution 0.8 ml 1.0 M HCl 0.5 ml 0.005 ml I 2 solution Using this scheme, your group can systematically double, triple, or even halve the concentration of acetone or H + for a given trial.

Interpreting your Data The rate of disappearance of I 2 is calculated from your experimental data using the equation rate = - [I 2 ]/ t This equation can be further simplified to rate = [I 2 ] i /t where t is simply the number of seconds elapsed from the start of the reaction (i.e., upon adding the I 2 ), and [I 2 ] i is the initial concentration of I 2. (Note: the initial concentration of I 2 is not 0.005 M!) Using the headers below, construct a table to summarize your experimental findings for the dependence of rate upon concentration. Trial # [acetone] [H + ] rate How do you use this table to learn more about the rate law? First, examine any pair of trials in which all concentrations are held constant. If your group performed any such trials, they are called replicates. If the calculated rate for each of these replicates is similar, their mere presence should bolster your confidence in your group s technique and methods. Next, look at a pair of trials in which the concentration of acid was held constant while the concentration of acetone was varied. The variation in rate, if any, associated with a pair of trials in which [acetone] is systematically varied should exhibit a simple pattern. If the concentration of acetone does not have any impact on the reaction rate, it can be dropped from the rate law entirely; such a reactant is known as a zero-order reactant. If [acetone] does appear to impact the reaction rate, you should carefully examine how, on a quantitative level, the rate is impacted. If doubling the acetone concentration doubles the rate, halving the acetone concentration halves the rate, etc., then the reaction is said to be first-order with respect to acetone. In such a case, the exponent x for acetone in the rate law would simply be equal to 1, and you ve just elucidated an important part of the rate law! If, on the other hand, doubling the concentration of acetone quadruples the reaction rate, you ve just identified the mathematical phenomenon of a second-order reactant, and the exponent associated with [acetone] should be noted as 2. You can use this same approach to determine the simple whole-number exponent for H +. (As you study more about the broad subject of chemical kinetics, you ll learn that some reactions exhibit rate laws with fractional, or even negative, exponents. Determining rate laws for these reactions requires calculations that go beyond the scope of this simpler, line-by-line examination of kinetics data.) Work with your group members to deduce the rate law for acetone iodination. How will your group use this rate law to calculate k, the rate constant? Report A brief, individually prepared report approximately 3-4 pages in length is due at the beginning of next week s lab period. It is a full report, consisting of All Sections. You have practiced each section of a lab report already, and quality work is expected. The majority of your report should be the Discussion section. Several of the questions in green, which you should answer in your notebook, are also good types of questions to address in the Discussion section. (The answers for some of the questions in green would be better answered in the Results section. Which questions are these?)

Glossary integrated rate law an expression for the time-dependent concentration of reactants and products in a reaction obtained by solving the rate law (see below); comparison of concentrations as a function of time with measured concentrations versus time is one way to determine the rate law rate constant the constant of proportionality between the reaction rate and the reactant concentrations to their reaction orders; for analogous rate laws (i.e., same reaction orders) the rate constant measures the speed of the reaction; the rate constant depends only on temperature rate law a generally empirical relationship between the rate of a reaction (see below) and the concentrations of the reactants, e.g., rate = v = k[a] x [B] y ; a rate law is defined by the reaction order of each reactant, e.g., x and y above, and the rate constant, k rate of reaction the speed with which a reaction proceeds expressed in terms of concentration of reactants consumed per unit time or concentration of products produced per unit time; if A is a reactant and C is a product, then the rate can be written as v =-Δ[A]/ Δ t = Δ [C]/ Δ t, for the limit Δ t 0; the rate generally depends on time, changing as the reaction proceeds