Study Guide for Electrochemistry 6.Pdf

Total Page:16

File Type:pdf, Size:1020Kb

Study Guide for Electrochemistry 6.Pdf Study Guide for CHEM 219/229 How to write a redox reaction using Electrochemical Cell notation: Terms to know: • Redox Reaction: A chemical reaction that involves the transfer of electrons between species, with one species losing electrons (being oxidized) and another species gaining electrons (being reduced). • Electrode: For the purposes of electrochemistry, a strip of metal. • Half- cell: An electrode submerged in a solution of ions of the same metal. • Electrochemical Cell: Two properly connected half cells. Two kinds: Galvanic and electrolytic o Galvanic Cell: An electrochemical cell that uses a chemical reaction to produce electrical energy. o Electrolytic Cell: An electrochemical cell that uses electrical energy to drive a chemical reaction. • Anode: The half-cell where oxidation takes place. • Cathode: The half-cell where reduction takes place. • Salt-bridge: A porous barrier (generally a U-tube) that allows ions to move between half-cells to complete the electrical circuit. General Cell Diagram: Electrode|Solution||Solution|Electrode • The single lines represent the phase boundary between each electrode and its solution • The double lines represent the salt bridge • The anode is always written on the left of the diagram, the cathode always on the right. • Example: o For the following reaction: Mg (s) + FeCl2 (aq) -> Fe (s) + MgCl2 (aq) o We start by assigning oxidation numbers: o Mg (s): . Mg O.N = 0 o FeCl2 (aq): . Fe O.N = +2 . Cl O.N = -1 o Fe(s): . Fe O.N = 0 o MgCl2 (s) . Mg O.N = +2 . Cl O.N = -1 o We can see that the Mg is being oxidized (it goes from a 0 to a +2 O.N), while the Fe is being reduced (goes from a +2 to a 0 O.N). • We can then break the redox reaction into half-reactions. One reduction half-reaction and one oxidation half-reaction: 2+ - Red: Mg (s) -> Mg (aq) + 2e 2+ - Ox: Fe (aq) + 2e -> Fe (s) • Notice that the Cl does not appear. Because it doesn’t change during the reaction, it is only a spectator ion and can be ignored. • Each of these half reactions can then be written as a half-cell, with the oxidation half-reaction being at the anode and reduction half-reaction being at the cathode: Anode|Solution||Solution|Cathode 2+ 2+ Fe(s)|Fe (aq)||Mg (aq)|Mg(s) .
Recommended publications
  • Cell Notation Practical Galvanic Cells -Batteries
    Basic Redox Vocabulary • Write reactions for each of the following: • oxidation of metallic nickel by BiO+ • reduction of Zn2+ by hydroxide ion • reaction of Fe 2+ with Hg2+ 2+ • reaction of Cd with NO2 • AgI acting as an oxidizing agent toward Sn 2+ • What’s wrong with • The oxidation of Cr by Cl- • The reduction of Co 2+ by Ag+ Cell Notation • As was noted earlier, galvanic cells normally consist of two distinct regions, one housing the oxidation half and the other the reduction half. There is a simplified notation form that allows one to represent the cell easily( text p 798- 799). • The oxidation is written on the left and the reduction on the right. starting with the anode material and ending with the cathode material. • phase boundaries represented with single vertical lines “ |” • the physical separation between the two half cells is a double v ertical line “||” if it’s a salt bridge and with a single broken vertical line, “!”, if it’s a liquid junction • within each have cell, the species are written in a reactant-product order, separated by commas if they are in the same phase. Acid/base components should be included • The electrode material may be actively participating in the redox chemistry (active electrode) or merely providing surface for the electron transfer (passive or inert electrode, usually graphite or Pt) • Represent the following as galvanic cells(assume the reactions are spontaneous as written) • Tl(s) + Cd 2+ ó Tl + + Cd(s) - 2+ 2+ • Pb(s) + MnO4 ó Pb + Mn (acid) 2+ 4+ • O2(g) + Sn ó H2O + Sn Practical Galvanic Cells -batteries • Batteries represent the most common application of the electrochemical cell.
    [Show full text]
  • Redox Models in Chemistry
    Redox models in chemistry A depiction of the conceptions held by secondary school students of redox reactions Lise-Lotte Österlund Department of Chemistry 901 87 Umeå Umeå 2010 Copyright©Lise-Lotte Österlund ISBN: 978-91-7459-053-1 ISSN: 1652-5051 Cover picture: Photographer, Lise-Lotte Österlund Printed by: VMC, KBC, Umeå University Umeå, Sweden 2010 T0 my family Abstract According to previous research, students show difficulties in learning redox reactions. By the historical development different redox models exist to explain redox reactions, the oxygen model, the hydrogen model, the electron model and the oxidation number model. This thesis reports about three studies concerning conceptions held by secondary school students of redox reactions. A textbook analysis is also included in the thesis. The first study was an investigation of the students’ use of redox models in inorganic contexts, their use of the activity series of metals, and the students’ ability to transfer redox knowledge. Then the students’ work with an open- ended biochemical task, where the students had access of the textbook was studied. The students talk about redox reactions, the questions raised by the students, what resources used to answer the questions and what kind of talk developed were investigated. A textbook analysis based on chemistry books from Sweden and one book from England was performed. The redox models used as well as the dealing with redox related learning difficulties was studied. Finally, the students’ conceptions about redox in inorganic, organic and biochemistry after completed chemistry courses were studied. The results show that the students were able to use the electron model as a tool to explain inorganic redox reactions and the mutuality of oxidation and reduction was fundamental.
    [Show full text]
  • Promotion Effects and Mechanism of Alkali Metals and Alkaline Earth
    Subscriber access provided by RES CENTER OF ECO ENVIR SCI Article Promotion Effects and Mechanism of Alkali Metals and Alkaline Earth Metals on Cobalt#Cerium Composite Oxide Catalysts for N2O Decomposition Li Xue, Hong He, Chang Liu, Changbin Zhang, and Bo Zhang Environ. Sci. Technol., 2009, 43 (3), 890-895 • DOI: 10.1021/es801867y • Publication Date (Web): 05 January 2009 Downloaded from http://pubs.acs.org on January 31, 2009 More About This Article Additional resources and features associated with this article are available within the HTML version: • Supporting Information • Access to high resolution figures • Links to articles and content related to this article • Copyright permission to reproduce figures and/or text from this article Environmental Science & Technology is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Environ. Sci. Technol. 2009, 43, 890–895 Promotion Effects and Mechanism such as Fe-ZSM-5 are more active in the selective catalytic reduction (SCR) of N2O by hydrocarbons than in the - ° of Alkali Metals and Alkaline Earth decomposition of N2O in a temperature range of 300 400 C (3). In recent years, it has been found that various mixed Metals on Cobalt-Cerium oxide catalysts, such as calcined hydrotalcite and spinel oxide, showed relatively high activities. Composite Oxide Catalysts for N2O One of the most active oxide catalysts is a mixed oxide containing cobalt spinel. Calcined hydrotalcites containing Decomposition cobalt, such as Co-Al-HT (9-12) and Co-Rh-Al-HT (9, 11), have been reported to be very efficient for the decomposition 2+ LI XUE, HONG HE,* CHANG LIU, of N2O.
    [Show full text]
  • Prebiological Evolution and the Metabolic Origins of Life
    Prebiological Evolution and the Andrew J. Pratt* Metabolic Origins of Life University of Canterbury Keywords Abiogenesis, origin of life, metabolism, hydrothermal, iron Abstract The chemoton model of cells posits three subsystems: metabolism, compartmentalization, and information. A specific model for the prebiological evolution of a reproducing system with rudimentary versions of these three interdependent subsystems is presented. This is based on the initial emergence and reproduction of autocatalytic networks in hydrothermal microcompartments containing iron sulfide. The driving force for life was catalysis of the dissipation of the intrinsic redox gradient of the planet. The codependence of life on iron and phosphate provides chemical constraints on the ordering of prebiological evolution. The initial protometabolism was based on positive feedback loops associated with in situ carbon fixation in which the initial protometabolites modified the catalytic capacity and mobility of metal-based catalysts, especially iron-sulfur centers. A number of selection mechanisms, including catalytic efficiency and specificity, hydrolytic stability, and selective solubilization, are proposed as key determinants for autocatalytic reproduction exploited in protometabolic evolution. This evolutionary process led from autocatalytic networks within preexisting compartments to discrete, reproducing, mobile vesicular protocells with the capacity to use soluble sugar phosphates and hence the opportunity to develop nucleic acids. Fidelity of information transfer in the reproduction of these increasingly complex autocatalytic networks is a key selection pressure in prebiological evolution that eventually leads to the selection of nucleic acids as a digital information subsystem and hence the emergence of fully functional chemotons capable of Darwinian evolution. 1 Introduction: Chemoton Subsystems and Evolutionary Pathways Living cells are autocatalytic entities that harness redox energy via the selective catalysis of biochemical transformations.
    [Show full text]
  • Voltaic Cells
    Voltaic Cells Tro Chapter 19 – Electrochemistry 19.3 Voltaic(or Galvanic) Cells: Generating Electricity from Spontaneous Chemical Reactions Electric Current Flowing Directly Between Atoms Tro, Chemistry: A Molecular Approach 2 Electrochemical Cells Voltaic (Galvanic) ΔG < 0 to Electrolytic Δ G > 0 uses electrical generate electrical energy. energy to drive non-spontaneous process. Electrochemical Cells • Oxidation and reduction half-reactions are kept separate in half-cells. • Electron flow through a wire along with ion flow through a solution constitutes an electric circuit. • It requires a conductive solid electrode to allow the transfer of electrons. – Through external circuit – Metal or graphite • Requires ion exchange between the Daniell Cell two half-cells of the system. – Electrolyte Definitions Anode Salt Bridge • Electrode where oxidation always occurs • An inverted, U-shaped tube containing a • More negatively charged electrode in strong electrolyte and connecting the two voltaic cell half-cells. • Typically made of metal that is oxidized Cathode • Electrode where reduction always occurs Potential Difference • More positively charged electrode in • The difference in potential energy voltaic cell between the reactants and products. • Typically metal that is produced by reduction (Caused by an electric field resulting from the charge difference on the two If the redox reaction involves the oxidation or electrodes.) reduction of an ion to a different oxidation state, or the oxidation or reduction of a gas, we Cell Potential (Ecell or emf) may use an inert electrode. • The potential difference between the anode and the cathode in a voltaic cell. • An inert electrode is one that not does participate in the reaction but just provides a surface on which the transfer of electrons can take place.
    [Show full text]
  • Galvanic Cell Notation • Half-Cell Notation • Types of Electrodes • Cell
    Galvanic Cell Notation ¾Inactive (inert) electrodes – not involved in the electrode half-reaction (inert solid conductors; • Half-cell notation serve as a contact between the – Different phases are separated by vertical lines solution and the external el. circuit) 3+ 2+ – Species in the same phase are separated by Example: Pt electrode in Fe /Fe soln. commas Fe3+ + e- → Fe2+ (as reduction) • Types of electrodes Notation: Fe3+, Fe2+Pt(s) ¾Active electrodes – involved in the electrode ¾Electrodes involving metals and their half-reaction (most metal electrodes) slightly soluble salts Example: Zn2+/Zn metal electrode Example: Ag/AgCl electrode Zn(s) → Zn2+ + 2e- (as oxidation) AgCl(s) + e- → Ag(s) + Cl- (as reduction) Notation: Zn(s)Zn2+ Notation: Cl-AgCl(s)Ag(s) ¾Electrodes involving gases – a gas is bubbled Example: A combination of the Zn(s)Zn2+ and over an inert electrode Fe3+, Fe2+Pt(s) half-cells leads to: Example: H2 gas over Pt electrode + - H2(g) → 2H + 2e (as oxidation) + Notation: Pt(s)H2(g)H • Cell notation – The anode half-cell is written on the left of the cathode half-cell Zn(s) → Zn2+ + 2e- (anode, oxidation) + – The electrodes appear on the far left (anode) and Fe3+ + e- → Fe2+ (×2) (cathode, reduction) far right (cathode) of the notation Zn(s) + 2Fe3+ → Zn2+ + 2Fe2+ – Salt bridges are represented by double vertical lines ⇒ Zn(s)Zn2+ || Fe3+, Fe2+Pt(s) 1 + Example: A combination of the Pt(s)H2(g)H Example: Write the cell reaction and the cell and Cl-AgCl(s)Ag(s) half-cells leads to: notation for a cell consisting of a graphite cathode - 2+ Note: The immersed in an acidic solution of MnO4 and Mn 4+ reactants in the and a graphite anode immersed in a solution of Sn 2+ overall reaction are and Sn .
    [Show full text]
  • Redox Potential Measurements M.J
    Redox Potential Measurements M.J. Vepraskas NC State University December 2002 Redox potential is an electrical measurement that shows the tendency of a soil solution to transfer electrons to or from a reference electrode. From this measurement we can estimate whether the soil is aerobic, anaerobic, and whether chemical compounds such as Fe oxides or nitrate have been chemically reduced or are present in their oxidized forms. Making these measurements requires three basic pieces of equipment: 1. Platinum electrode 2. Voltmeter 3. Reference electrode The basic set-up is shown below: Voltmeter 456 mv Soil surface Reference Pt wire electrode Fig. 1. The Pt wire is buried into the soil to be in contact with the soil solution. The reference electrode must also be in contact with the soil solution. It has a ceramic tip, which can be placed in the soil, or the electrode can be placed in a salt bridge, which is itself placed in the soil. Wires from both the Pt electrode and reference electrode are connected to the voltmeter. Pt Electrodes Platinum electrodes consist of a small piece of platinum wire that is soldered or fused to wire made another metal. Platinum conducts electrons from the soil solution to the wire to which it is attached. Platinum is used because it is assumed to be an inert metal. This means it does not give up its own electrons (does not oxidize) to the wire or soil solution. Iron containing materials such as steel will oxidize themselves and send their own electrons to the voltmeter. As a result the voltage we measure will not result solely from electrons being transferred to or from the soil.
    [Show full text]
  • Origins of Life in the Universe Zackary Johnson
    11/4/2007 Origins of Life in the Universe Zackary Johnson OCN201 Fall 2007 [email protected] Zackary Johnson http://www.soest.hawaii.edu/oceanography/zij/education.html Uniiiversity of Hawaii Department of Oceanography Class Schedule Nov‐2Originsof Life and the Universe Nov‐5 Classification of Life Nov‐7 Primary Production Nov‐9Consumers Nov‐14 Evolution: Processes (Steward) Nov‐16 Evolution: Adaptation() (Steward) Nov‐19 Marine Microbiology Nov‐21 Benthic Communities Nov‐26 Whale Falls (Smith) Nov‐28 The Marine Food Web Nov‐30 Community Ecology Dec‐3 Fisheries Dec‐5Global Ecology Dec‐12 Final Major Concepts TIMETABLE Big Bang! • Life started early, but not at the beginning, of Earth’s Milky Way (and other galaxies formed) history • Abiogenesis is the leading hypothesis to explain the beginning of life on Earth • There are many competing theories as to how this happened • Some of the details have been worked out, but most Formation of Earth have not • Abiogenesis almost certainly occurred in the ocean 20‐15 15‐94.5Today Billions of Years Before Present 1 11/4/2007 Building Blocks TIMETABLE Big Bang! • Universe is mostly hydrogen (H) and helium (He); for Milky Way (and other galaxies formed) example –the sun is 70% H, 28% He and 2% all else! Abundance) e • Most elements of interest to biology (C, N, P, O, etc.) were (Relativ 10 produced via nuclear fusion Formation of Earth Log at very high temperature reactions in large stars after Big Bang 20‐13 13‐94.7Today Atomic Number Billions of Years Before Present ORIGIN OF LIFE ON EARTH Abiogenesis: 3 stages Divine Creation 1.
    [Show full text]
  • 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.
    [Show full text]
  • The Structural and Chemical Origin of the Oxygen Redox Activity in Layered and Cation-Disordered Li-Excess Cathode Materials
    ARTICLES PUBLISHED ONLINE: 30 MAY 2016 | DOI: 10.1038/NCHEM.2524 The structural and chemical origin of the oxygen redox activity in layered and cation-disordered Li-excess cathode materials Dong-Hwa Seo1,2†, Jinhyuk Lee1,2†, Alexander Urban2, Rahul Malik1,ShinYoungKang1 and Gerbrand Ceder1,2,3* Lithium-ion batteries are now reaching the energy density limits set by their electrode materials, requiring new paradigms for Li+ and electron hosting in solid-state electrodes. Reversible oxygen redox in the solid state in particular has the potential to enable high energy density as it can deliver excess capacity beyond the theoretical transition-metal redox- capacity at a high voltage. Nevertheless, the structural and chemical origin of the process is not understood, preventing the rational design of better cathode materials. Here, we demonstrate how very specific local Li-excess environments around oxygen atoms necessarily lead to labile oxygen electrons that can be more easily extracted and participate in the practical capacity of cathodes. The identification of the local structural components that create oxygen redox sets a new direction for the design of high-energy-density cathode materials. ver the past two decades, lithium-ion battery technology has why it is observed with some metals and not with others. The contributed greatly to human progress and enabled many of specific nature of our findings reveals a clear and exciting path Othe conveniences of modern life by powering increasingly towards creating the next generation of cathode materials with capable portable electronics1. However, with the increasing com- substantially higher energy density than current cathode materials.
    [Show full text]
  • 3297 Chapter 13.Indd
    Inert Electrodes The zinc anode and copper cathode of a Daniell cell and the silver and chromium electrodes in Figure 13.4 are all metals and can act as electrical conductors. However, some redox reactions involve oxidizing and reducing agents that are not solid metals but, instead, are dissolved electrolytes or gases and, therefore, cannot be used as electrodes. To construct a voltaic cell that will use these oxidizing and reducing agents, you have to use inert electrodes. An inert electrode is an electrode made from a material that is neither a reactant nor a product of the redox reaction. Instead, the inert electrode can carry a current and provide a surface on which redox reactions can occur. Figure 13.5 shows a cell that contains one example of an inert electrode—a platinum electrode. The complete balanced equation, net ionic equation, and half-reactions for this cell are given below. complete balanced equation: Pb(s) + 2FeCl3(aq) → 2FeCl2(aq) + PbCl2(aq) net ionic equation: Pb(s) + 2Fe3+(aq) → 2Fe2+(aq) + Pb2+(aq) oxidation half-reaction: Pb(s) → Pb2+(aq) + 2e– reduction half-reaction: Fe3+(aq) + e– → Fe2+(aq) The anode is the lead electrode. Lead atoms lose electrons that remain in the electrode while the lead(II) ions dissolve in the solution in the same way that the anode did in previous example. However, the reduction half-reaction involves iron(III) ions that accept an electron from the platinum inert electrode and become iron(II) ions. The platinum atoms in the electrode (cathode) remain unchanged. Voltmeter e- e- Anode Salt bridge Cathode (-) K+ (+) Pb Cl- Pt 2e- e- Fe3+ Pb Fe2+ Pb2+ PbCl2 FeCl3 FeCl2 Figure 13.5 This cell uses an inert electrode to conduct electrons.
    [Show full text]
  • Thermochemical Energy Storage by Water-Splitting Via Redox Reaction of Alkali Metals
    Available online at www.sciencedirect.com ScienceDirect Energy Procedia 49 ( 2014 ) 927 – 934 SolarPACES 2013 Thermochemical energy storage by water-splitting via redox reaction of alkali metals H. Miyaokaa,*, T. Ichikawab, Y. Kojimab aInstitute for Sustainable Sciences and Development, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8530, Japan bInstitute for Advanced Materials Research, Hiroshima University1-3-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8530, Japan Abstract The reaction cycles for water-splitting based on redox reactions of alkali metals are composed of four reactions, which are hydrogen generation by solid-liquid reaction, metal separation by thermolysis, oxygen generation by hydrolysis, and phase transition of the metal. Although all the cycles theoretically require more than 1000 qC in thermodynamic equilibrium condition, the reaction temperature are reduced to below 800 qCn− by no equilibrium techniques using phase transition of metal vapor. In this work, thermodynamic analyses are performed by using the parameters such as operating temperature and partial pressures of the products obtained by the experiments to determine that the alkali metal redox cycles are potential hydrogen production technique as thermochemical energy storage. © 2013 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (©http://creativecommons.org/licenses/by-nc-nd/3.0/ 2013 The Authors. Published by Elsevier Ltd.). Selection and and peer peer review review by by the the scientific scientific conference conference committee committee of SolarPACES of SolarPACES 2013 under 2013 responsibility under responsibility of PSE AG. of PSE AG. Final manuscript published as received without editorial corrections.
    [Show full text]