Chapter 14. CHEMICAL EQUILIBRIUM
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Basic Design Data, of Column for Absorption Of
j833 Index – a acetyl radical 741 breakthrough curves for H2S adsorption on a absorption 108 acid aerosols 567 molecular sieve 132, 133 – activity and activity coefficients, in acid–base catalyzed reactions 11 – calculation of lads,ideal, HTZ, and LUB chloroform 111 acid catalyst 11 based on breakthrough curves 135 – basic design data, of column for absorption acidity 10 – capillary condensation of CO2 in water 116 acid-catalyzed reaction 652 –– and adsorption/desorption hysteresis 126 – Bunsen absorption coefficient 110 acid-soluble polymers 653 – competitive 128 – – fi chemical absorption of CO2 in N- acrolein 30, 476, 476, 479, 481, 483, 701 design of a xed-bed adsorption process 131 methyldiethanolamine 112, 113 acrylamide 28, 29, 487 – design of processes 130–135 – CO2 in water, and subsequent bicarbonate acrylic acid 140, 466, 467, 479, 481–483 – desorption 131 formation 110 acrylonitrile 462, 466, 467, 486–487 – dissociative 128 – design of columns 113–116 activation energy 24, 34, 201, 203, 215, 711 – equilibrium of a binary system on zeolite 128 – equilibria of chemical absorption 108 – apparent activation energy of diffusion – estimation of slope of breakthrough curve 132 – equilibria of physical absorption, processes 229, 230, 232 – height of mass transfer zone HTZ 132 comparison 109 – for chain transfer 807 – hysteresis loop during – fl – –– gas velocity and ooding of absorption correlation between activation energy and adsorption and desorption of N2 in a column 115 reaction enthalpy for a reversible cylindrical pore 127 – height -
Characteristics of Chemical Equilibrium
Characteristics of Chemical Equilibrium Chapter 14: Chemical Equilibrium © 2008 Brooks/Cole 1 © 2008 Brooks/Cole 2 Equilibrium is Dynamic Equilibrium is Independent of Direction of Approach Reactants convert to products N2(g) + 3 H2(g) 2 NH3(g) a A + b B c C + d D Species do not stop forming OR being destroyed Rate of formation = rate of removal Concentrations are constant. © 2008 Brooks/Cole 3 © 2008 Brooks/Cole 4 Equilibrium and Catalysts The Equilibrium Constant For the 2-butene isomerization: H3C CH3 H3C H C=C C=C H H H CH3 At equilibrium: rate forward = rate in reverse An elementary reaction, so: kforward[cis] = kreverse[trans] © 2008 Brooks/Cole 5 © 2008 Brooks/Cole 6 1 The Equilibrium Constant The Equilibrium Constant At equilibrium the concentrations become constant. We had: kforward[cis] = kreverse[trans] kforward [trans] or = kreverse [cis] kforward [trans] Kc = = = 1.65 (at 500 K) kreverse [cis] “c” for concentration based © 2008 Brooks/Cole 7 © 2008 Brooks/Cole 8 The Equilibrium Constant The Equilibrium Constant For a general reaction: a A + b B c C + d D [NO]2 N2(g) + O2(g) 2 NO(g) Kc = Products raised to [N2] [O2] stoichiometric powers… k [C]c [D]d forward …divided by reactants Kc = = a b kreverse [A] [B] raised to their stoichiometric [SO ] 1 2 powers 8 S8(s) + O2(g) SO2(g) Kc = [O2] © 2008 Brooks/Cole 9 © 2008 Brooks/Cole 10 Equilibria Involving Pure Liquids and Solids Equilibria in Dilute Solutions [Solid] is constant throughout a reaction. density g / L • pure solid concentration = mol. -
Laboratory 1: Chemical Equilibrium 1
1 Laboratory 1: Chemical Equilibrium 1 Reading: Olmstead and Williams, Chemistry , Chapter 14 (all sections) Purpose: The shift in equilibrium position of a chemical reaction with applied stress is determined. Introduction Chemical Equilibrium No chemical reaction goes to completion. When a reaction stops, some amount of reactants remain. For example, although we write → ← 2 CO 2 (g) 2 CO (g) + O 2 (g) (1) as though it goes entirely to products, at 2000K only 2% of the CO 2 decomposes. A chemical reaction reaches equilibrium when the concentrations of the reactants and products no longer change with time. The position of equilibrium describes the relative amounts of reactants and products that remain at the end of a chemical reaction. The position of equilibrium for reaction (1) is said to lie with the reactants, or to the left, because at equilibrium very little of the carbon dioxide has reacted. On the other hand, in the reaction → ← H2 (g) + ½ O2 (g) H2O (g) (2) the equilibrium position lies very far to the right since only very small amounts of H 2 and O 2 remain after the reaction reaches equilibrium. Since chemists often wish to maximize the yield of a reaction, it is vital to determine how to control the position of the equilibrium. The equilibrium position of a reaction may shift if an external stress is applied. The stress may be in the form of a change in temperature, pressure, or the concentration of one of the reactants or products. For example, consider a flask with an equilibrium mixture of CO 2, CO, and O 2, as in reaction (1). -
The Practice of Chemistry Education (Paper)
CHEMISTRY EDUCATION: THE PRACTICE OF CHEMISTRY EDUCATION RESEARCH AND PRACTICE (PAPER) 2004, Vol. 5, No. 1, pp. 69-87 Concept teaching and learning/ History and philosophy of science (HPS) Juan QUÍLEZ IES José Ballester, Departamento de Física y Química, Valencia (Spain) A HISTORICAL APPROACH TO THE DEVELOPMENT OF CHEMICAL EQUILIBRIUM THROUGH THE EVOLUTION OF THE AFFINITY CONCEPT: SOME EDUCATIONAL SUGGESTIONS Received 20 September 2003; revised 11 February 2004; in final form/accepted 20 February 2004 ABSTRACT: Three basic ideas should be considered when teaching and learning chemical equilibrium: incomplete reaction, reversibility and dynamics. In this study, we concentrate on how these three ideas have eventually defined the chemical equilibrium concept. To this end, we analyse the contexts of scientific inquiry that have allowed the growth of chemical equilibrium from the first ideas of chemical affinity. At the beginning of the 18th century, chemists began the construction of different affinity tables, based on the concept of elective affinities. Berthollet reworked this idea, considering that the amount of the substances involved in a reaction was a key factor accounting for the chemical forces. Guldberg and Waage attempted to measure those forces, formulating the first affinity mathematical equations. Finally, the first ideas providing a molecular interpretation of the macroscopic properties of equilibrium reactions were presented. The historical approach of the first key ideas may serve as a basis for an appropriate sequencing of -
Anal Chem 458.309A Week 5.Pdf
§ Verify this behavior algebraically using the reaction quotient, Q § In one particular equilibrium state of this system, à the following concentrations exist: § Suppose that the equilibrium is disturbed by adding dichromate to the 2- solution to increase the concentration of [Cr2O7 ] from 0.10 to 0.20 M. à In what direction will the reaction proceed to reach equilibrium? § Because Q > K à the reaction must go to the left to decrease the numerator and increase the denominator, until Q = K § If a reaction is at equilibrium and products are added (or reactants are removed), à the reaction goes to the left. § If a reaction is at equilibrium and reactants are added (or products are removed), à the reaction goes to the right § The effect of temperature on K: § The term eΔS°/R is independent of T à ΔS is constant at least over a limited temperature range § If ΔHo is positive, à The term e-ΔH°/RT increases with increasing temperature § If ΔHo is negative, à The term e-ΔH°/RT decreases with increasing temperature § The effect of temperature on K: § If the temperature is raised, à The equilibrium constant of an endothermic reaction (ΔHo>0) increases à The equilibrium constant of an exothermic reaction (Δho<0) decreases § If the temperature is raised, à an endothermic reaction is favored § If the temperature is raised, then heat is added to the system. à The reaction proceeds to partially offset this heat à an endothermic reaction à Le Châtelier’s principle Solubility product § The equilibrium constant for the reaction in which a solid salt dissolves to give its constituent ions in solution. -
Answer Key Chapter 16: Standard Review Worksheet – + 1
Answer Key Chapter 16: Standard Review Worksheet – + 1. H3PO4(aq) + H2O(l) H2PO4 (aq) + H3O (aq) + + NH4 (aq) + H2O(l) NH3(aq) + H3O (aq) 2. When we say that acetic acid is a weak acid, we can take either of two points of view. Usually we say that acetic acid is a weak acid because it doesn’t ionize very much when dissolved in water. We say that not very many acetic acid molecules dissociate. However, we can describe this situation from another point of view. We could say that the reason acetic acid doesn’t dissociate much when we dissolve it in water is because the acetate ion (the conjugate base of acetic acid) is extremely effective at holding onto protons and specifically is better at holding onto protons than water is in attracting them. + – HC2H3O2 + H2O H3O + C2H3O2 Now what would happen if we had a source of free acetate ions (for example, sodium acetate) and placed them into water? Since acetate ion is better at attracting protons than is water, the acetate ions would pull protons out of water molecules, leaving hydroxide ions. That is, – – C2H3O2 + H2O HC2H3O2 + OH Since an increase in hydroxide ion concentration would take place in the solution, the solution would be basic. Because acetic acid is a weak acid, the acetate ion is a base in aqueous solution. – – 3. Since HCl, HNO3, and HClO4 are all strong acids, we know that their anions (Cl , NO3 , – and ClO4 ) must be very weak bases and that solutions of the sodium salts of these anions would not be basic. -
Main Criteria: AP Chemistry Course Description Secondary Criteria: Jove Subject: Science Grade: 9-12 Correlation Options: Show Correlated Adopted: 2013
Main Criteria: AP Chemistry Course Description Secondary Criteria: JoVE Subject: Science Grade: 9-12 Correlation Options: Show Correlated Adopted: 2013 Outline Level 1 AP.C.1. Big Idea 1: The chemical elements are fundamental building materials of matter, and all matter can be understood in terms of arrangements of atoms. These atoms retain their identity in chemical reactions. Outline Level 2 EU.1.A. All matter is made of atoms. There are a limited number of types of atoms; these are the elements. Outline Level 3 EK.1.A.1. Molecules are composed of specific combinations of atoms; different molecules are composed of combinations of different elements and of combinations of the same elements in differing amounts and proportions. Outline Level 4 1.A.1.a. The average mass of any large number of atoms of a given element is always the same for a given element. JoVE • Freezing-Point Depression to Determine an Unknown Compound • Introduction to Mass Spectrometry • MALDI-TOF Mass Spectrometry • Tandem Mass Spectrometry Outline Level 4 1.A.1.b. A pure sample contains particles (or units) of one specific atom or molecule; a mixture contains particles (or units) of more than one specific atom or molecule. JoVE • Calibration Curves • Capillary Electrophoresis (CE) • Chromatography-Based Biomolecule Purification Methods • Column Chromatography • Conducting Reactions Below Room Temperature • Cyclic Voltammetry (CV) • Degassing Liquids with Freeze-Pump-Thaw Cycling • Density Gradient Ultracentrifugation • Determining the Density of a Solid and Liquid -
Drugs and Acid Dissociation Constants Ionisation of Drug Molecules Most Drugs Ionise in Aqueous Solution.1 They Are Weak Acids Or Weak Bases
Drugs and acid dissociation constants Ionisation of drug molecules Most drugs ionise in aqueous solution.1 They are weak acids or weak bases. Those that are weak acids ionise in water to give acidic solutions while those that are weak bases ionise to give basic solutions. Drug molecules that are weak acids Drug molecules that are weak bases where, HA = acid (the drug molecule) where, B = base (the drug molecule) H2O = base H2O = acid A− = conjugate base (the drug anion) OH− = conjugate base (the drug anion) + + H3O = conjugate acid BH = conjugate acid Acid dissociation constant, Ka For a drug molecule that is a weak acid The equilibrium constant for this ionisation is given by the equation + − where [H3O ], [A ], [HA] and [H2O] are the concentrations at equilibrium. In a dilute solution the concentration of water is to all intents and purposes constant. So the equation is simplified to: where Ka is the acid dissociation constant for the weak acid + + Also, H3O is often written simply as H and the equation for Ka is usually written as: Values for Ka are extremely small and, therefore, pKa values are given (similar to the reason pH is used rather than [H+]. The relationship between pKa and pH is given by the Henderson–Hasselbalch equation: or This relationship is important when determining pKa values from pH measurements. Base dissociation constant, Kb For a drug molecule that is a weak base: 1 Ionisation of drug molecules. 1 Following the same logic as for deriving Ka, base dissociation constant, Kb, is given by: and Ionisation of water Water ionises very slightly. -
Unit IV Outiline
CHEMISTRY 111 LECTURE EXAM IV Material PART 1 CHEMICAL EQUILIBRIUM Chapter 14 I Dynamic Equilibrium I. In a closed system a liquid obtains a dynamic equilibrium with its vapor state Dynamic equilibrium: rate of evaporation = rate of condensation II. In a closed system a solid obtains a dynamic equilibrium with its dissolved state Dynamic equilibrium: rate of dissolving = rate of crystallization II Chemical Equilibrium I. EQUILIBRIUM A. BACKGROUND Consider the following reversible reaction: a A + b B ⇌ c C + d D 1. The forward reaction (⇀) and reverse (↽) reactions are occurring simultaneously. 2. The rate for the forward reaction is equal to the rate of the reverse reaction and a dynamic equilibrium is achieved. 3. The ratio of the concentrations of the products to reactants is constant. B. THE EQUILIBRIUM CONSTANT - Types of K's Solutions Kc Gases Kc & Kp Acids Ka Bases Kb Solubility Ksp Ionization of water Kw Hydrolysis Kh Complex ions βη Page 1 General Keq Page 2 C. EQUILIBRIUM CONSTANT For the reaction, aA + bB ⇌ cC + dD The equilibrium constant ,K, has the form: [C]c [D]d Kc = [A]a [B]b D. WRITING K’s 1. N2(g) + 3 H2(g) ⇌ 2 NH3(g) 2. 2 NH3(g) ⇌ N2(g) + 3 H2(g) E. MEANING OF K 1. If K > 1, equilibrium favors the products 2. If K < 1, equilibrium favors the reactants 3. If K = 1, neither is favored F. ACHIEVEMENT OF EQUILIBRIUM Chemical equilibrium is established when the rates of the forward and reverse reactions are equal. CO(g) + 3 H2(g) ⇌ CH4 + H2O(g) Initial amounts moles H 2 Equilibrium amounts moles CO moles CH = moles water 4 Time Page 3 G. -
Theoretical Problem Icho 2019
Candidate: AAA-1 THEORETICAL EXAM Making science together! 2019-07-26 51st IChO – Theoretical Exam 1 Candidate: AAA-1 General instructions This theoretical exam booklet contains 60 pages. You may begin writing as soon as the Start command is given. You have 5 hours to complete the exam. All results and answers must be clearly written in pen in their respective designed areas on the exam papers. Answers written outside the answer boxes will not be graded. If you need scratch paper, use the backside of the exam sheets. Remember that nothing outside the designed areas will be graded. Use only the pen and calculator provided. The official English version of the exam booklet is available upon request and serves for clarification only. If you need to leave the exam room (to use the toilet or have a snack), wave the corresponding IChO card. An exam supervisor will come to accompany you. For multiple-choice questions: if you want to change your answer, fill the answer box completely and then make a new empty answer box next to it. The supervisor will announce a 30-minute warning before the Stop command. You must stop your work immediately when the Stop command is announced. Failure to stop writing by ½ minute or longer will lead to nullification of your theoretical exam. After the Stop command has been given, place your exam booklet back in your exam envelope, then wait at your seat. The exam supervisor will come to seal the envelope in front of you and collect it. GOOD LUCK! 51st IChO – Theoretical Exam 2 Candidate: AAA-1 Table of Contents This theoretical exam is composed of 9 independent problems, as follows. -
Electrochemistry –An Oxidizing Agent Is a Species That Oxidizes Another Species; It Is Itself Reduced
Oxidation-Reduction Reactions Chapter 17 • Describing Oxidation-Reduction Reactions Electrochemistry –An oxidizing agent is a species that oxidizes another species; it is itself reduced. –A reducing agent is a species that reduces another species; it is itself oxidized. Loss of 2 e-1 oxidation reducing agent +2 +2 Fe( s) + Cu (aq) → Fe (aq) + Cu( s) oxidizing agent Gain of 2 e-1 reduction Skeleton Oxidation-Reduction Equations Electrochemistry ! Identify what species is being oxidized (this will be the “reducing agent”) ! Identify what species is being •The study of the interchange of reduced (this will be the “oxidizing agent”) chemical and electrical energy. ! What species result from the oxidation and reduction? ! Does the reaction occur in acidic or basic solution? 2+ - 3+ 2+ Fe (aq) + MnO4 (aq) 6 Fe (aq) + Mn (aq) Steps in Balancing Oxidation-Reduction Review of Terms Equations in Acidic solutions 1. Assign oxidation numbers to • oxidation-reduction (redox) each atom so that you know reaction: involves a transfer of what is oxidized and what is electrons from the reducing agent to reduced 2. Split the skeleton equation into the oxidizing agent. two half-reactions-one for the oxidation reaction (element • oxidation: loss of electrons increases in oxidation number) and one for the reduction (element decreases in oxidation • reduction: gain of electrons number) 2+ 3+ - 2+ Fe (aq) º Fe (aq) MnO4 (aq) º Mn (aq) 1 3. Complete and balance each half reaction Galvanic Cell a. Balance all atoms except O and H 2+ 3+ - 2+ (Voltaic Cell) Fe (aq) º Fe (aq) MnO4 (aq) º Mn (aq) b. -
Chapter 15 Chemical Equilibrium
Chapter 15 Chemical Equilibrium Learning goals and key skills: Explain what is meant by chemical equilibrium and how it relates to reaction rates Write the equilibrium-constant expression for any reaction Convert Kc to Kp and vice versa Relate the magnitude of an equilibrium constant to the relative amounts of reactants and products present in an equilibrium mixture. Manipulate the equilibrium constant to reflect changes in the chemical equation Write the equilibrium-constant expression for a heterogeneous reaction Calculate an equilibrium constant from concentration measurements Predict the direction of a reaction given the equilibrium constant and the concentrations of reactants and products Calculate equilibrium concentrations given the equilibrium constant and all but one equilibrium concentration Calculate equilibrium concentrations given the equilibrium constant and the starting concentrations Use Le Chatelier’s principle to predict how changing the concentrations, volume, or temperature of a system at equilibrium affects the equilibrium position. The Concept of Equilibrium Chemical equilibrium occurs when a reaction and its reverse reaction proceed at the same rate. 1 Concept of Equilibrium • As a system approaches equilibrium, both the forward and reverse reactions are occurring. • At equilibrium, the forward and reverse reactions are proceeding at the same rate. • Once equilibrium is achieved, the amount of each reactant and product remains constant. The same equilibrium is reached whether we start with only reactants (N2 and H2) or with only product (NH3). Equilibrium is reached from either direction. 2 The Equilibrium Constant • Consider the generalized reaction aA + bB cC + dD The equilibrium expression for this reaction would be [C]c[D]d K = c [A]a[B]b Since pressure is proportional to concentration for gases in a closed system, the equilibrium expression can also be written c d (PC) (PD) Kp = a b (PA) (PB) Chemical equilibrium occurs when opposing reactions are proceeding at equal rates.