Composition of the Universe

Total Page:16

File Type:pdf, Size:1020Kb

Composition of the Universe KEY for Unit 4 - Fundamentals of Atomic Structure: Electrons in Atoms and the Periodic Table The Periodic Law - when elements are arranged according to their atomic number, their chemical and physical properties show repeatable trends. The vertical columns are called groups and the horizontal rows are called periods. There are four categories of groups (although some people do not separate the Noble gases from the Main Group elements): 1. Representative (also Main Group Elements) 2. Transition elements 3. Inner transition (also Lanthanide and Actinide) 4. Noble gasses The letters A and B in the group distinguish families: A = representative and B = transition. One of the most useful features of the periodic table is that it summarizes properties in a succinct manner. Take a look at a periodic table and think about the following. Where are metals found? See periodic table below – elements in various shades of blue. Where are nonmetals found? See periodic table below – elements in yellow. Where are the metalloids found? See periodic table below – elements in green. Are all main group elements metals, nonmetals, metalloids? All Group 1A (except H) and 2A elements are metals. In groups 3A – 8A degree of metallic character increasing down the groups (with groups 7A and 8A all being listed as nonmetals). Metalloids are in the p-block of the periodic table running in a staircase pattern from boron (B) down and to the right.. Locate the following groups in the periodic table. Alkali metals (Group 1A or simply Group 1), alkaline earth metals (Group 2A or simply Group 2), noble gases [in the past called the inert gases] (Group 8A or simply Group 18), halogens (Group 7A or simply Group 17), chalcogens (Group 6A or simply Group 16), coinage metals (Group 1B or simply Group 11), and list the semimetals [the metalloids] boron (B), silicon (Si), germanium (Ge), arsenic (As), antimony (Sb), and tellurium (Te). Polonium (Po) is often considered a metalloid, too). Check three different periodic tables and see if they all list the same metalloids. Think about why there might not be universal agreement about which elements to call metalloids (think about the definition of metalloids, or semi-metals as they are sometimes called). Metalloids are intermediate in behavior between metals and non-metals, and since metallic behavior varies across a period and up (or down) a group, we should not be surprised if there is not universal agreement on EXACTLY where the dividing line should be drawn. Some elements 61 that are listed as metalloids look quite metallic in appearance (like antimony, Sb) whereas others display properties more similar to nonmetals (example the brittle nature of silicon, Si). Figure: a reasonably current modern periodic table – new elements are added above atomic number 109, but that area of the periodic table has no naturally occurring elements. Guided Discovery Assignment 4-1 This guided discovery activity can be completed by using the information provided below. 1. Using the following list of ionization energies, IE (given in kJ per mole), prepare a graph of ionization energy (on the y-axis) vs. atomic number (on the x-axis): H, 1312; He, 2372; Li, 520; Be, 900; B, 801; C, 1086; N, 1402; O, 1314; F, 1681; Ne, 2081; Na, 496; Mg, 738; Al, 578; Si, 786; P, 1012; S, 1000; Cl, 1251; Ar, 1520; K, 419; Ca, 590; Ga, 579; Ge, 762; As, 944; Se, 941; Br, 1140; Kr, 1351 2. Make sure that you recognize that there is a jump in atomic number (from number 20 to number number 31) in the graph provided below. 3. Think about what this comparison shows. 4. On the discussion date you should be prepared to answer questions about this assignment in the classroom. 62 Highest oxidation is determined (in large part) by the number of valence electrons that are present. However, other properties (such as IE, EA, EN, and atomic size) have an influence. examples: N can become +5 (loss of 2s22p3) but F will not become +7 (it won't lose 2s22p5) but Cl will become +7 (loss of 3s23p5) DONE IN CLASS Guided Discovery Assignment 4-2 This guided discovery activity can be completed by using the information provided below. 1. Using the following list of ionization energies, IE (given in kJ per mole), see if you can relate the changes in ionizations energies of each element (from first to second to . ) to the electronic structure of that element: Ionization Energies of Several Elements Element 1st IE 2nd IE 3rd IE 4th IE 5th IE 6th IE 7th IE Na 496 4,560 Mg 738 1,450 7730 Al 577 1,816 2,744 11,600 Si 786 1,577 3,228 4,354 16,100 P 1,060 1,890 2,905 4,950 6,270 21,000 S 999 2,260 3,375 4,565 6,950 8,490 27,000 Cl 1,256 2,295 3,850 5,160 6,560 9,360 11,000 Ar 1,520 2,665 3,945 5,770 7,230 8,780 12,000 63 2. Consider how the answer to question number one relates to Guided Discovery 2 above. Think carefully about the graph of "HCON" (Highest Common Oxidation Number), shown above. 3. On the discussion date you should be prepared to answer questions about this assignment in the classroom. DONE IN CLASS 64.
Recommended publications
  • Stability of Coinage Metals Interacting with C60
    nanomaterials Article Stability of Coinage Metals Interacting with C60 Navaratnarajah Kuganathan 1,2,* , Ratnasothy Srikaran 3 and Alexander Chroneos 1,2 1 Department of Materials, Imperial College London, London SW7 2AZ, UK; [email protected] 2 Faculty of Engineering, Environment and Computing, Coventry University, Priory Street, Coventry CV1 5FB, UK; [email protected] 3 Department of Chemistry, University of Jaffna, Sir. Pon Ramanathan Road, Thirunelvely, Jaffna 40000, Srilanka; [email protected] * Correspondence: [email protected] or [email protected] Received: 27 September 2019; Accepted: 17 October 2019; Published: 18 October 2019 Abstract: Buckminsterfullerene (C60) has been advocated as a perfect candidate material for the encapsulation and adsorption of a variety of metals and the resultant metallofullerenes have been considered for the use in different scientific, technological and medical areas. Using spin-polarized density functional theory together with dispersion correction, we examine the stability and electronic structures of endohedral and exohedral complexes formed between coinage metals (Cu, Ag and Au) and both non-defective and defective C60. Encapsulation is exoergic in both forms of C60 and their encapsulation energies are almost the same. Exohedral adsorption of all three metals is stronger than that of endohedral encapsulation in the non-defective C60. Structures and the stability of atoms interacting with an outer surface of a defective C60 are also discussed. As the atoms are stable both inside and outside the C60, the resultant complexes can be of interest in different scientific and medical fields. Furthermore, all complexes exhibit magnetic moments, inferring that they can be used as spintronic materials.
    [Show full text]
  • Influence of Relativistic Effects on Hydrolysis Of
    RADIOCHEMISTRY, STABLE ISOTOPES, NUCLEAR ANALYTICAL METHODS, GENERAL CHEMISTRY 57 INFLUENCE OF RELATIVISTIC EFFECTS ON HYDROLYSIS OF THE HEAVY METAL CATIONS Maria Barysz1/, Jerzy Leszczyński1/, Barbara Zielińska, Aleksander Bilewicz 1/ Department of Quantum Chemistry, Faculty of Chemistry, Nicolaus Copernicus University, Toruń, Poland The process of hydrolysis is related to the interac- Some models for the explanation of this phe- tion between the oxygen in the water molecule and nomenon have been proposed but none of them the metal cation as shown in the following reac- appears to be sufficiently adequate and complete tion [1]: [l, 7]. On the other hand, certain empirical corre- n(n1)+−++ M(H2x O)→+ M(H 2x1 O)− (OH) H lations between experimental data and parameters Therefore, the tendency to hydrolyze increases which characterize cations suggest that a success- with increasing oxidation state of the cation and ful model of the phenomenon must explicitly in- decreasing ionic radius. This is understandable clude relativistic effects. For heavy ions these ef- because with decreasing M-O distance, the polar- fects should be important for predicting the struc- izing effect of smaller cation on the O-H bond in ture and strength of the cation-water complexes. the aqua ligand increases, which, in turn results in The present paper aims at showing the role of the easier loss of the proton from the hydrated cation. relativistic effects on the structure and energetics The ability to hydrolysis has been discussed in many of these complexes and their ability to release pro- papers in terms of the charge (Z) and ionic radii tons.
    [Show full text]
  • (BB) Ru Metallacycle with Coinage Metal Cations
    Chemical Science View Article Online EDGE ARTICLE View Journal | View Issue Expansion of the (BB)pRu metallacycle with coinage metal cations: formation of B–M–Ru–B Cite this: Chem. Sci.,2018,9,2601 (M ¼ Cu, Ag, Au) dimetalacyclodiboryls† Bennett J. Eleazer,a Mark D. Smith,a Alexey A. Popov *b and Dmitry V. Peryshkov *a In this work, we introduce a novel approach for the selective assembly of heterometallic complexes by unprecedented coordination of coinage metal cations to strained single ruthenium–boron bonds on a surface of icosahedral boron clusters. M(I) cations (M ¼ Cu, Ag, and Au) insert into B–Ru bonds of the (BB)–carboryne complex of ruthenium with the formation of four-membered B–M–Ru–B metalacycles. Results of theoretical calculations suggest that bonding within these metalacycles can be best described as unusual three-center-two-electron B–M/Ru interactions that are isolobal to B–H/Ru borane coordination for M ¼ Cu and Ag, or the pairs of two-center-two electron B–Au and Au–Ru interactions Creative Commons Attribution 3.0 Unported Licence. for M ¼ Au. These transformations comprise the first synthetic route to exohedral coinage metal boryl complexes of icosahedral closo-{C2B10} clusters, which feature short Cu–B (2.029(2) A)˚ and Ag–B Received 12th January 2018 (2.182(3) A)˚ bonds and the shortest Au–B bond (2.027(2) A)˚ reported to date. The reported heterometallic Accepted 3rd February 2018 complexes contain Cu(I) and Au(I) centers in uncharacteristic square-planar coordination environments. DOI: 10.1039/c8sc00190a These findings pave the way to rational construction of a broader class of multimetallic architectures rsc.li/chemical-science featuring M–B bonds.
    [Show full text]
  • Interaction Between Trinuclear Regium Complexes of Pyrazolate and Anions, a Computational Study
    International Journal of Molecular Sciences Article Interaction between Trinuclear Regium Complexes of Pyrazolate and Anions, a Computational Study Ibon Alkorta 1,* , José Elguero 1, Cristina Trujillo 2 and Goar Sánchez-Sanz 3,4,* 1 Instituto de Química Médica, CSIC, Juan de la Cierva, 3, E-28006 Madrid, Spain; [email protected] 2 Trinity Biomedical Sciences Institute, School of Chemistry, Trinity Dublin College, D02 R590 Dublin 2, Ireland; [email protected] 3 Irish Centre of High-End Computing, Grand Canal Quay, Dublin 2, Ireland 4 School of Chemistry, University College Dublin, Belfield, D02 HP83 Dublin 4, Ireland * Correspondence: [email protected] (I.A.); [email protected] (G.S.-S.) Received: 8 October 2020; Accepted: 23 October 2020; Published: 28 October 2020 Abstract: The geometry, energy and electron density properties of the 1:1, 1:2 and 1:3 complexes between cyclic (Py-M)3 (M = Au, Ag and Cu) and halide ions (F−, Cl− and Br−) were studied using Møller Plesset (MP2) computational methods. Three different configurations were explored. In two of them, the anions interact with the metal atoms in planar and apical dispositions, while in the last configuration, the anions interact with the CH(4) group of the pyrazole. The energetic results for the 1:2 and 1:3 complexes are a combination of the specific strength of the interaction plus a repulsive component due to the charge:charge coulombic term. However, stable minima structures with dissociation barriers for the anions indicate that those complexes are stable and (Py-M)3 can hold up to three anions simultaneously.
    [Show full text]
  • Periodic Variations in the Catalytic Properties of Metals the INFLUENCE of SOLID STATE PARAMETERS on ADSORPTION and CATALYSIS
    Periodic Variations in the Catalytic Properties of Metals THE INFLUENCE OF SOLID STATE PARAMETERS ON ADSORPTION AND CATALYSIS By G. C. Bond, D.s~.,F.R.I.C. Research Laboratories, Johnson Matthey & Co Limited (2) The first row Group VIII metals (base Of the one hundred or so elements in the metals): Fe, Co, Ni. Periodic Table no less than spventy-jive (3) The second and third row Group VIII are metals, but of these only the twelve in metals (platinum group metals) : Ru, Groups VIIl and IB have important Rh, Pd, Os, Ir, Pt. catalytic properties. The marked changes in these properties on proceed- Comparison of Groups VIII and IB ing either certically or horizontally There are dramatic differences between the through the groups is discussed in terns catalytic properties of the Group IB metals of the periodic variation of the solid- and those metals lying adjacent in Group state properties of the mijtals. VIII : these differences are particularly marked with hydrogenation and similar It is now well established that the occur- reactions. Silver and gold are totally unable rence of significant and useful catalytic to activate hydrogen and hence to catalyse properties is largely confined to the elements reactions involving hydrogen, while their lying in Groups VIII and IB of the Periodic immediate neighbours to the left, palladium Table. Other elements of the transition series and platinum, are among the best known are able to act catalytically, but because of the hydrogenation catalysts. This simple ob- great thermochemical difficulty of reducing servation constitutes the most vivid possible them to the metallic state, and of keeping demonstration of the existence of an electronic them reduced, they do not find any practical factor in catalysis, since geometrically speak- applications.
    [Show full text]
  • Some Interesting Facts of Coinage Metals Tarasankar Pal Department of Chemistry, Indian Institute of Technology, Kharagpur, Kharagpur 712302
    Nano Science…. Some Interesting Facts of Coinage Metals Tarasankar Pal Department of Chemistry, Indian Institute of Technology, Kharagpur, Kharagpur 712302 Email: [email protected] Mendeleev designed the periodic table (1869) with a vision. His focus was very important that was supported by the discoveries of scientists in the later stage. He placed heavier nickel before lighter cobalt even though he was arranging the elements as per their increasing atomic weights (at. wt.). This apparent anomalous arrangement was justified by the discovery of atomic number (at. no.) of the elements at a later stage. Thus the position of cobalt (at. no. 27) and nickel (at. no. 28) was justified. Again, he did not place any element instead kept a void position in between manganese and rhenium in the manganese group. He himself realized that the element was not discovered by then. But below manganese, under the void place, he intelligently placed rhenium (Re). His realization gave birth to the first technically prepared element technetium (Tc). Thus manganese group was completed. Scientists realized that Tc, for its small half life, T1/2 (211,000 yrs) value, disappeared from earth’s crust and first man made element was born. This discovery filled a gap in the periodic table, and the fact that no stable isotopes of technetium exist. This explains its natural absence on Earth (and the gap). He also located the positions (one room for lanthanide and beneath that are actinide elements) of lanthanide and actinide elements below Sc and Y. In so doing he completed the group of alkaline earth metal with the representative element Sc.
    [Show full text]
  • Theoretical Study of the Adsorption of Benzene on Coinage Metals
    Theoretical study of the adsorption of benzene on coinage metals Werner Reckien, Melanie Eggers and Thomas Bredow* Full Research Paper Open Access Address: Beilstein J. Org. Chem. 2014, 10, 1775–1784. Mulliken Center for Theoretical Chemistry, Rheinische doi:10.3762/bjoc.10.185 Friedrich-Wilhelms-Universität Bonn, Beringstr. 4, 53115 Bonn, Germany Received: 28 February 2014 Accepted: 15 July 2014 Email: Published: 04 August 2014 Thomas Bredow* - [email protected] This article is part of the Thematic Series "Chemical templates". * Corresponding author Guest Editor: S. Höger Keywords: adsorption; benzene; coinage metals; density functional theory; © 2014 Reckien et al; licensee Beilstein Institute. dispersion correction; template License and terms: see end of document. Abstract The adsorption of benzene on the M(111), M(100) and M(110) surfaces of the coinage metals copper (M = Cu), silver (M = Ag) and gold (M = Au) is studied on the basis of density functional theory (DFT) calculations with an empirical dispersion correction (D3). Variants of the Perdew–Burke–Ernzerhof functionals (PBE, RPBE and RevPBE) in combination with different versions of the dispersion correction (D3 and D3(BJ)) are compared. PBE-D3, PBE-D3(BJ) and RPBE-D3 give similar results which exhibit a good agreement with experimental data. RevPBE-D3 and RevPBE-D3(BJ) tend to overestimate adsorption energies. The inclusion of three-center terms (PBE-D3(ABC)) leads to a slightly better agreement with the experiment in most cases. Vertical adsorbate–substrate distances are calculated and compared to previous theoretical results. The observed trends for the surfaces and metals are consistent with the calculated adsorption energies.
    [Show full text]
  • Gold's Structural Versatility Within Complex Intermetallics: from Hume
    Chemistry Conference Papers, Posters and Chemistry Presentations 2013 Gold’s Structural Versatility within Complex Intermetallics: From Hume-Rothery to Zintl and even Quasicrystals Gordon J. Miller Iowa State University, [email protected] Srinivasa Thimmaiah Iowa State University Volodymyr Smetana Ames Laboratory, [email protected] Andriy Palasyuk Iowa State University, [email protected] Qisheng Lin Ames Laboratory, [email protected] Follow this and additional works at: http://lib.dr.iastate.edu/chem_conf Part of the Materials Chemistry Commons, Organic Chemistry Commons, Other Chemistry Commons, and the Physical Chemistry Commons Recommended Citation Miller, Gordon J.; Thimmaiah, Srinivasa; Smetana, Volodymyr; Palasyuk, Andriy; and Lin, Qisheng, "Gold’s Structural Versatility within Complex Intermetallics: From Hume-Rothery to Zintl and even Quasicrystals" (2013). Chemistry Conference Papers, Posters and Presentations. 9. http://lib.dr.iastate.edu/chem_conf/9 This Article is brought to you for free and open access by the Chemistry at Iowa State University Digital Repository. It has been accepted for inclusion in Chemistry Conference Papers, Posters and Presentations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Gold’s Structural Versatility within Complex Intermetallics: From Hume- Rothery to Zintl and even Quasicrystals Abstract Recent exploratory syntheses of polar intermetallic compounds containing gold have established gold’s tremendous ability to stabilize new phases with diverse and fascinating structural motifs. In particular, Au-rich polar intermetallics contain Au atoms condensed into tetrahedra and diamond-like three-dimensional frameworks. In Au-poor intermetallics, on the other hand, Au atoms tend to segregate, which maximizes the number of Au-heteroatom contacts.
    [Show full text]
  • The Physics Behind Chemistry, and the Periodic Table
    The physics behind chemistry, and the Periodic Table Pekka Pyykkö∗ Department of Chemistry, University of Helsinki, POB 55 (A. I. Virtasen aukio 1), 00014 Helsinki, Finland E-mail: Pekka.Pyykko@helsinki.fi Contents 1. Introduction 2 2. The levels of theory 4 2.1. The Dirac-Coulomb-Breit (DCB) Hamiltonian 4 2.2. The next level: Introducing the QED terms 5 2.2.1. Qualitative discussion 5 2.2.2. Vacuum polarization 7 2.2.3. Self-energy: The benchmark 8 2.2.4. Approximate self-energy approaches 12 2.2.5. Summary of numerical results for atoms 19 ∗To whom correspondence should be addressed 1 2.3. Accurate calculations on diatomics 22 2.4. Further small terms and curiosities 24 2.4.1. The finite nuclear size 24 2.4.2. Nuclear electric polarizability 24 2.4.3. ’Nuclear relativity’ 25 2.4.4. Magnetic and hyperfine effects 26 2.4.5. Retardation at large distances 27 3. The Periodic Table 27 4. Conclusion 32 1. Introduction Theoretical chemistry could be seen as a bridge from the real physics of the physicists to the real chemistry of the experimental chemists. We hence expect that any measurable property of any chemical object could, in principle, be calculated to arbitrary accuracy, if the relevant physical laws are known. Moreover, as put by Sidgwick,1 ’The chemist must resist the temptation to make his own physics; if he does, it will be bad physics–justas the physicist has sometimes been tempted to make his own chemistry, and then it was bad chemistry.’ The first step was the Schrödinger equation since the 1920:ies.
    [Show full text]
  • Mind Over Matter?
    book reviews rather than around a diverse set of practical is also well known. I would have liked to have lessons borne from experience, the authors seen more in this chapter. Oxygen is too have limited this book’s contribution to an pivotal an element to be treated lightly and alternative view of how decision-makers needs to have been addressed from a modern might confront complex and contested viewpoint. It is the only element, apart from BETTMANN/CORBIS environmental and science policies. I fluorine, that can react with so many others. Roger Pielke Jr is at the Center for Science and Unlike fluorine, however, it is not so reactive Technology Policy Research, University of as to become exotic, and it is more flexible Colorado/Cooperative Institute for Research in than fluorine in the kinds of bonds it forms. Environmental Sciences, Boulder, Oxygen can, in effect, feel the pulse of the rest Colorado 80309, USA. of the elements quite accurately, and it does this in increasingly subtle ways, such as by participating in hydrogen bonds. The organization of the elements into the periodic table is treated competently, as is Mind the synthesis of new elements in the ‘atom factories’ in Berkeley and Dubna, and these over matter? chapters contain a lot of information. Ball’s The Ingredients: A Guided Tour description of isotopes is particularly good, of the Elements and I do not believe that I have seen such by Philip Ball an imaginative handling of this usually Oxford University Press: 2002. 228 pp. £13.99 Golden touch: the tale of King Midas highlights stodgy topic.
    [Show full text]
  • CHEMISTRY for BIOLOGY
    3.00_Chemistry of Biology Biology I Periodic Table of the Elements Slides 33-44 1 Organizing Elements (Patterns) The Periodic Table of Elements is a way of organizing the elements in relation to each other so it is easy to find elements that have similar properties. 2 Periodic Table of the Elements How do you read the PERIODIC TABLE? 3 Mass Number 4 Periods Each row is called a “period” The elements in each period have the same number of electron shells Hint: A period comes at the end of a sentence--a horizontal line. 5 www.chem4kids.com Periods (Rows) Properties Seven periods on a periodic table (numbered from the top down) Atomic numbers and atomic masses increase as you move from the left to the right in a period All atoms of the elements in the same period have the same number of orbitals/levels All atoms of the elements in a specific period have that respective number of orbitals/levels 6 Periods The horizontal rows of the periodic table are called periods. Elements in a period are not alike in properties. The first element in a period is usually an active solid, and the last element in a period is always an inactive gas. 7 Periods Rows Atomic size (number of protons) decreases from left to right across a period. Atomic mass (number of protons) increases from left to right across a period. 8 Periods Rows Metals are on the left Non-metals are on the right 9 Groups or Families Group 1 = 1 electron Group 8 = 8 electrons Group 2 = 2 electrons Except for He, it has 2 electrons Each column is called a “group” or family.
    [Show full text]
  • United States Patent (19) (11) 4,374,008 Natansohn Et Al
    United States Patent (19) (11) 4,374,008 Natansohn et al. 45) Feb. 15, 1983 (54) PROCESS FOR SEPARATING TUNGSTEN 56) References Cited FROM CONAGEMETALS U.S. PATENT DOCUMENTS 4,278,643 7/1981 Natansohn et al. ................... 423/54 (75) Inventors: Samuel Natansohn, Sharon; Gary Czupryna, Salem, both of Mass. 4,287,159 9/1981 Natansohn et al. ................... 423/54 FOREIGN PATENT DOCUMENTS (73) Assignee: GTE Laboratories incorporated, 2025211 12/1971 Fed. Rep. of Germany ...... 204/109 Waltham, Mass. Primary Examiner-R. L. Andrews Attorney, Agent, or Firm-Jerry F. Janssen Appl. No.: 269,192 (21) 57 ABSTRACT 22) Filed: Jun. 1, 1981 A process for cleanly separating coinage metals from alloys of coinage metals and tungsten comprises electro 51 Int. Cl. ........................... C25C1/08; C25C 1/22 winning the coinage metal from an electrolyte solution (52 U.S. C. .................................... 204/109; 204/112; which is contacted with an ion exchange resin to selec 75/101 BE tively remove the tungsten. (58 Field of Search ................... 75/101 BE; 204/109, 204/112 11 Claims, 1 Drawing Figure U.S. Patent Feb. 15, 1983 4,374,008 4,374,008. 2 are placed in contact with an anode plate 35 which rests PROCESS FOR SEPARATING TUNGSTEN FROM in the anode chamber basket 30. COINAGE METALS A cathode plate 50 rests on the bottom of the electro winning cell 10 and the entire assembly is filled with BACKGROUND OF THE INVENTION 5 electrolyte solution 25. In the embodiment of the pres This invention relates to processes for separating ent invention wherein silver is separated from silver metals.
    [Show full text]