INTRODUCTORY CHEMISTRY Concepts and Critical Thinking Sixth Edition by Charles H
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Naming Polyatomic Ions and Acids Oxyanions
Oxyanions Naming Polyatomic Ions and Oxyanions Acids Oxyanions- negative ions containing Oxyanions may contain the prefix oxygen. “hypo-”, less than, or “per-”, more than. These have the suffix “-ate” or “-ite” For example - “-ate” means it has more oxygen atoms ClO4 Perchlorate bonded, “-ite” has less - ClO3 Chlorate For example - ClO2 Chlorite 2- SO4 sulfate ClO- Hypochlorite 2- SO3 sulfite Acids Naming acids Naming Acids Certain compounds produce H+ ions in Does it contain oxygen? water, these are called acids. If it does not, it gets the prefix “hydro-” and If it does contain an oxyanion, then the suffix “-ic acid” replace the ending. You can recognize them because the neutral compound starts with “H”. HCl If the ending was “–ate”, add “-ic acid” Hydrochloric acid If the ending was “–ite”, add “-ous acid” For example HCl, H2SO4, and HNO3. HF Don’t confuse a polyatomic ion with a H2SO4 Sulfuric Acid Hydrofluoric acid neutral compound. H2SO3 Sulfurous Acid HCN HCO - is hydrogen carbonate, not an acid. 3 Hydrocyanic acid Examples Examples Nomenclature (naming) of Covalent compounds HNO3 HNO3 Nitric Acid HI HI Hydroiodic acid H3AsO4 H3AsO4 Arsenic Acid HClO2 HClO2 Chlorous Acid 1 Determining the type of bond Covalent bonding is very Covalent bonding is very First, determine if you have an ionic different from ionic naming compound or a covalent compound. similar to ionic naming A metal and a nonmetal will form an You always name the one that is least Ionic names ignored the subscript ionic bond. electronegative first (furthest from because there was only one possible Compounds with Polyatomic ions form fluorine) ratio of elements. -
Pp-03-25-New Dots.Qxd 10/23/02 2:41 PM Page 778
pp-03-25-new dots.qxd 10/23/02 2:41 PM Page 778 778 PRAESODYMIUM PRAESODYMIUM [7440–10–0] Symbol Pr; atomic number 59; atomic weight 140.908; a lanthanide–series rare earth element; belongs to the cerium group of rare earths; electron con- figuration [Xe] 4f36s2; partially filled f subshell; valence states +3, +4; most 3+ stable oxidation state +3; electrode potential E°/V (aq) for Pr + 3e¯ ↔ Pr is –2.35 V; atomic radius 1.828 Å; first ionization potential 5.46 eV; one natu- rally–occurring isotope, Pr–141; twenty–nine artificial radioactive isotopes known in the mass range 124, 126–140 and 142–154; the longest–lived isotope Pr–143, t1/2 13.57 day, and the shortest–lived isotope Pr–124, t1/2 1.2 second. History, Occurrence, and Uses Mosander extracted from the mineral lanthana a rare earth fraction, named didymia in 1841. In 1879, Boisbaudran separated a rare earth oxide called samaria (samarium oxide) from the didymia fraction obtained from the mineral samarskite. Soon after that in 1885, Baron Auer von Welsbach iso- lated two other rare earths from didymia. He named them as praseodymia (green twin) and neodymia (new twin) after their source didymia (twin). The name praseodymium finally was assigned to this new element, derived from the two Greek words, prasios meaning green and didymos meaning twin. Praseodymium occurs in nature associated with other rare earths in a rel- atively high abundance. It is more abundant than some common metals such as silver, gold, or antimony. The average concentration of this metal in the earth’s crust is estimated to be 8.2 mg/kg. -
Hypochlorous Acid Handling
Hypochlorous Acid Handling 1 Identification of Petitioned Substance 2 Chemical Names: Hypochlorous acid, CAS Numbers: 7790-92-3 3 hypochloric(I) acid, chloranol, 4 hydroxidochlorine 10 Other Codes: European Community 11 Number-22757, IUPAC-Hypochlorous acid 5 Other Name: Hydrogen hypochlorite, 6 Chlorine hydroxide List other codes: PubChem CID 24341 7 Trade Names: Bleach, Sodium hypochlorite, InChI Key: QWPPOHNGKGFGJK- 8 Calcium hypochlorite, Sterilox, hypochlorite, UHFFFAOYSA-N 9 NVC-10 UNII: 712K4CDC10 12 Summary of Petitioned Use 13 A petition has been received from a stakeholder requesting that hypochlorous acid (also referred 14 to as electrolyzed water (EW)) be added to the list of synthetic substances allowed for use in 15 organic production and handling (7 CFR §§ 205.600-606). Specifically, the petition concerns the 16 formation of hypochlorous acid at the anode of an electrolysis apparatus designed for its 17 production from a brine solution. This active ingredient is aqueous hypochlorous acid which acts 18 as an oxidizing agent. The petitioner plans use hypochlorous acid as a sanitizer and antimicrobial 19 agent for the production and handling of organic products. The petition also requests to resolve a 20 difference in interpretation of allowed substances for chlorine materials on the National List of 21 Allowed and Prohibited Substances that contain the active ingredient hypochlorous acid (NOP- 22 PM 14-3 Electrolyzed water). 23 The NOP has issued NOP 5026 “Guidance, the use of Chlorine Materials in Organic Production 24 and Handling.” This guidance document clarifies the use of chlorine materials in organic 25 production and handling to align the National List with the November, 1995 NOSB 26 recommendation on chlorine materials which read: 27 “Allowed for disinfecting and sanitizing food contact surfaces. -
WO 2014/029634 Al 27 February 2014 (27.02.2014) P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2014/029634 Al 27 February 2014 (27.02.2014) P O P C T (51) International Patent Classification: DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, C09C 1/02 (2006.01) HN, HR, HU, ID, IL, ΓΝ , IS, JP, KE, KG, KN, KP, KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, (21) International Application Number: MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, PCT/EP20 13/066666 OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, (22) International Filing Date: SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, 8 August 2013 (08.08.2013) TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (25) Filing Language: English (84) Designated States (unless otherwise indicated, for every (26) Publication Language: English kind of regional protection available): ARIPO (BW, GH, (30) Priority Data: GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, SZ, TZ, 1218 1089.9 20 August 2012 (20.08.2012) EP UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, 61/693,350 27 August 2012 (27.08.2012) US TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, LU, LV, (71) Applicant: OMYA INTERNATIONAL AG [CH/CH]; MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, Baslerstrasse 42, CH-4665 Oftringen (CH). -
On the Solubility of Radium Sulfate and Carbonate
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Chalmers Publication Library THESIS FOR THE DEGREE OF LICENTIATE OF ENGINEERING On the solubility of radium sulfate and carbonate Artem Vasilyevich Matyskin Nuclear Chemistry Department of Chemistry and Chemical Engineering CHALMERS UNIVERSITY OF TECHNOLOGY Gothenburg, Sweden 2016 On the solubility of radium sulfate and carbonate © ARTEM VASILYEVICH MATYSKIN, 2016 Technical report number: 2016:04 ISSN number: 1652-943X Nuclear Chemistry Department of Chemistry and Chemical Engineering Chalmers University of Technology SE – 412 96 Göteborg Sweden Telephone +46(0)31-772 1000 Cover: Radium sulfate powder Chalmers Reproservice Gothenburg, Sweden 2016 On the solubility of radium sulfate and carbonate Artem V. Matyskin Nuclear Chemistry Department of Chemistry and Chemical Engineering Chalmers University of Technology Abstract Radium is one of the most toxic elements and its concentration in different human activities and migration from man-made wastes provokes a strong interest in environmental science. To be able to model the migration process, reliable experimental thermodynamic data of radium compounds are needed. In this work details of the safe radium source disassembly which were previously used in brachytherapy are described and different methods for conversion of RaSO4 into aqueous solution are reviewed. The method of choice included three cycles of RaSO4 heating in 1.5 M Na2CO3 up to 85 ºC, cooling and subsequent removal of supernatant. X-ray diffraction studies showed that the method allows the synthesis of amorphous RaCO3, which can be dissolved in mineral acid. Gamma spectrometric measurements showed that most of the initial RaSO4 was 210 converted into solution and that 7 ± 1 % of the initial Pb was co-precipitated with RaCO3. -
Proceedings of the Indiana Academy of Science
A Comparison of Halogeno and Oxyacids L53 A COMPARISON OF HALOGENO AND OXYACIDS J. A. Nieuwland and T. H. Vaughn, University of Notre Dame In a recent paper originating in this department and sent to one of the chemical journals for publication the term "fluo acid" was used to designate a flourine containing acid which could be considered as having been formed by substituting two flourine atoms for each oxygen atom in an oxyacid. Criticism of this term on the ground that it was novel and unusual resulted. The paper mentioned being essentially organic in its nature it was impossible to explain the matter sufficiently except as a separate discussion. The purpose of this paper is to make an attempt to establish the term "halogeno acid" as a general name for acids in which the halogens may be considered to replace the oxygen in oxyacids and to establish the terms, fluo, chloro, bromo, and iodo as the specific names of these acids where the halogen involved is flourine, chlorine, bromine, and iodine respectively. As a matter of fact these names have been used in several cases and are accepted terms for those cases, i.e., fluoboric acid, bromostannic acid, fluoplumbic acid, fluosilicic acid, etc. When various molecular portions of water are added to the anhydrides of the acid forming elements, the several oxyacids are produced. B 2 3 +H 2 0^2HB0 2 B 2 2 +3H 2 0->2H 3 B0 3 In an analogous manner when the halogen acids are added to the halogen compounds corresponding to the anhydrides of the acid forming elements, the halogeno acids are formed. -
Atoms, Molecules, Ions, and Inorganic Nomenclature
Atoms, Molecules, Ions, and Inorganic Nomenclature Brown, LeMay Ch 2 AP Chemistry Monta Vista High School 2.2: Evidence for the Atomic Theory 1. J.J. Thomson’s cathode ray tube: discovery of electrons and the e- charge-to-mass ratio ¶ In a vacuum chamber, flow of high voltage (emitted from cathode to anode) is deflected by magnetic & electrical fields (animation: http://highered.mcgraw-hill.com/olcweb/cgi/pluginpop.cgi?it=swf::100%::100%::/sites/dl/free/ 0072512644/117354/01_Cathode_Ray_Tube.swf::Cathode%20Ray%20Tube) 2 2. Robert Millikan’s oil drop: determines charge of e- (and thus the mass) ¶ “Atomized” drops of oil picked up small charges (integral numbers), and balanced oil drops in an electrical & gravitational field http://cwx.prenhall.com/petrucci/medialib/media_portfolio/text_images/004_MILLIKANOIL.MOV 3. Ernest Rutherford’s gold foil: discovery of nucleus as center of positive charge ¶ Alpha particles from radioactive source are deflected from positive gold atom nuclei http://www.mhhe.com/physsci/ chemistry/animations/ chang_2e/ rutherfords_experiment.swf 2.3: Structure of the Atom Figure 1: Subatomic particles (Table 2.1; 1 amu = 1.66054 x 10-24 g). Subatomic Charge Location Mass particle Proton, p+ +1.6 x 10-19 C nucleus 1.0073 amu Neutron, n None nucleus 1.0087 amu Electron, e- -1.6 x 10-19 C e- cloud 5.486 x 10-4 amu 5 Vocabulary n Atomic number: number of p+ (determines the element) n Mass number: sum of p+ and n (determines the isotope) n Isotopes: atoms of an element that differ in the number of neutrons n Isobars: atoms of different elements with same atomic mass but different atomic number. -
And Inter-Protein Couplings of Backbone Motions Underlie
www.nature.com/scientificreports OPEN Intra- and inter-protein couplings of backbone motions underlie protein thiol-disulfde exchange cascade Received: 26 July 2018 Wenbo Zhang1,3, Xiaogang Niu2,3, Jienv Ding1,3,5, Yunfei Hu2,3,6 & Changwen Jin1,2,3,4 Accepted: 6 October 2018 The thioredoxin (Trx)-coupled arsenate reductase (ArsC) is a family of enzymes that catalyzes the Published: xx xx xxxx reduction of arsenate to arsenite in the arsenic detoxifcation pathway. The catalytic cycle involves a series of relayed intramolecular and intermolecular thiol-disulfde exchange reactions. Structures at diferent reaction stages have been determined, suggesting signifcant conformational fuctuations along the reaction pathway. Herein, we use two state-of-the-art NMR methods, the chemical exchange saturation transfer (CEST) and the CPMG-based relaxation dispersion (CPMG RD) experiments, to probe the conformational dynamics of B. subtilis ArsC in all reaction stages, namely the enzymatic active reduced state, the intra-molecular C10–C82 disulfde-bonded intermediate state, the inactive oxidized state, and the inter-molecular disulfde-bonded protein complex with Trx. Our results reveal highly rugged energy landscapes in the active reduced state, and suggest global collective motions in both the C10–C82 disulfde-bonded intermediate and the mixed-disulfde Trx-ArsC complex. Protein thiol-disulfde exchange reactions play fundamental roles in living systems, represented by the thiore- doxin (Trx) and glutaredoxin (Grx) systems that maintain the cytoplasmic reducing environment, the protein DsbA that catalyzes the formation of protein disulfde bonds in bacterial periplasm, as well as the protein disulfde isomerase (PDI) proteins that facilitate correct disulfde bonding1–5. -
Humidity-Sensing Component Composition
Patentamt JEuropaischesEuropean Patent Office © Publication number: 0 242 834 Office europeen des brevets A2 © EUROPEAN PATENT APPLICATION © Application number: 87105802.0 © Int.CI.3: G 01 N 27/12 @ Dateoffiling: 21.04.87 © Priority: 24.04.86 JP 93211/86 ©Applicant: MITSUBISHI GAS CHEMICAL COMPANY, INC. 24.04.86 JP 93212/86 5-2,Marunouchi2-chomeChiyoda-Ku 23.12.86 JP 305392/86 Tokyo(JP) © Inventor: Sugio, Akitoshi © Dateof publication of application: 382-155, Besho Ohaza-Sashiougiryo 28.10.87 Bulletin 87/44 Ohmiya-shiSaitama-Ken(JP) © Designated Contracting States: © Inventor: Shimomura.Tadashi FR GB 11 05-21, Higashifukai Nagareyama-shi Chiba-Ken(JP) @ Inventor: Wakabayashi, Hidechika 6-101, Nishlkubocho 15-chome Tokiwadaira Matsudo-shl Chiba-Ken(JP) © Inventor: Kondo,Osamu 25-15-201, Niijyuku 5-chome Katsushika-ku Tokyo(JP) @ Inventor: Ogasawara, Kazuharu 1 1 -1 6, Kanamachi 5-chome Katsushika-ku Tokyo(JP) © Inventor: Nishizawa, Chiharu 17-1,Kanegasaku Matsudo-shl Chiba-Ken(JP) © Representative: Blumbach Weser Bergen Kramer Zwirner Hoffmann Patentanwalte Radeckestrasse43 D-8000Munchen60(DE) Humidity-sensing component composition. © A humidity-sensing component composition includes a metallic oxide and a chalcogen oxyacid salt represented by a general formula AxByOz where A is one of an alkali metal and an alkaline earth metal, B is one of sulphur, selenium, and tellurium, O is oxygen, x is 1 to 2, y 1 to 5, and z 2 to 7. The chalcogen oxyacid salt is blended by an amount of 0.01 to 99.99 mol% in the metallic oxide with the sum of the metallic oxide and the chalcogen oxyacid salt as a reference. -
AAAS. the American Association for the Advancement of Science Was
A AAAS. The American Association for the Advancement of Science was movement through a planetary atmosphere to provide thermal protection founded in 1848 and incorporated in 1874. Its objectives are to further the to the underlying structure. See also Ablating Material. work of scientists, to facilitate cooperation among them, to foster scientific freedom and responsibility, to improve the effectiveness of science in ABRASION. All metallic and nonmetallic surfaces, no matter how promoting human welfare, to advance education in science, and to increase smooth, consist of minute serrations and ridges that induce a cutting or public understanding and appreciation for the importance and promise of tearing action when two surfaces in contact move with respect to each the methods of science in human progress. The AAAS head quarters is other. This wearing of the surfaces is termed abrasion. Undesirable abrasion in Washington, DC. Additional information on the AAAS can be found at may occur in bearings and other machine elements, but abrasion is also http://www.aaas.org/ and http://www.sciencemag.org/ . adapted to surface finishing and machining, where the material is too hard to be cut by other means, or where precision is a primary requisite. ABACA. The sclerenchyma bundles from the sheathing leaf bases of Temperature is a significant factor: friction may raise the temperature of Musa textilis, a plant closely resembling the edible banana plant. These the surface layers to the point where they become subject to chemical bundles are stripped by hand, after which they are cleaned by drawing over attack. Abrasion causes deterioration of many materials, especially of a rough knife. -
Evidence Against Stabilization of the Transition State Oxyanion by a Pka-Perturbed RNA Base in the Peptidyl Transferase Center
Evidence against stabilization of the transition state oxyanion by a pKa-perturbed RNA base in the peptidyl transferase center K. Mark Parnell*, Amy C. Seila†, and Scott A. Strobel*‡§ Departments of *Molecular Biophysics and Biochemistry, †Genetics, and ‡Chemistry, Yale University, 260 Whitney Avenue, New Haven, CT 06520-8114 Edited by Harry F. Noller, University of California, Santa Cruz, CA, and approved July 16, 2002 (received for review April 8, 2002) The crystal structure of the ribosomal 50S subunit from Haloarcula activity, suggesting that 23S and 5S rRNA may constitute the marismortui in complex with the transition state analog CCdA- bulk of the peptidyl transferase center (8). phosphate-puromycin (CCdApPmn) led to a mechanistic proposal The most unambiguous evidence that the active site of the wherein the universally conversed A2451 in the ribosomal active ribosome is comprised of RNA came from the 2.4-Å crystal site acts as an ‘‘oxyanion hole’’ to promote the peptidyl transferase structure of the Haloarcula marismortui 50S ribosomal subunit reaction [Nissen, P., Hansen, J., Ban, N., Moore, P.B., and Steitz, T.A. reported by Ban et al. (9) and Nissen et al. (10). The structure of the (2000) Science 289, 920–929]. In the model, close proximity (3 Å) 50S subunit complexed with the transition-state analog CCdA- between the A2451 N3 and the nonbridging phosphoramidate phosphate-puromycin (CCdApPmn) was vital to this structural oxygen of CCdApPmn suggested that the carbonyl oxyanion identification. CCdApPmn includes the minimal components of formed during the tetrahedral transition state is stabilized by both peptidyl transferase substrates (11). CCdA binds the P site, and hydrogen bonding to the protonated A2451 N3, the pKa of which puromycin binds the A site (Fig. -
Chemistry of Uo2 Fuel Dissolution in Relation to the Disposal of Used Nuclear Fuel
AECL-1 0395 ATOMIC ENERGY L'fNERGIE ATOMIQUE OF CANADA LIMITED DU CANADA LIMITEE CHEMISTRY OF U02 FUEL DISSOLUTION IN RELATION TO THE DISPOSAL OF USED NUCLEAR FUEL CHIMIE DE LA DISSOLUTION DU COMBUSTIBLE D'U02 EN RAPPORT AVEC LE STOCKAGE PERMANENT DU COMBUSTIBLE NUCLEAIRE USf S. Sunder, D. W. Shoesmith Whiteshell Laboratories Laboratoires de Whiteshell Pinawa, Manitoba ROE 1LO September 1991 septembre i-;fII 4.t .i I~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Copyrightof Canada©Atomic Energy L~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~mited, 1991.~~~~~~~~~~~~~~~~~~~~~~~~~ AECL RESEARCH CHEMISTRY OF U02 FUEL DISSOLUTION IN RELATION TO THE DISPOSAL OF USED NUCLEAR FUEL by S. Sunder and D.W. Shoesmith Whiteshell Laboratories Pinava, Manitoba ROE iLO 1991 AECL-10395 CHIMIE DE LA DISSOLUTION DU COMBUSTIBLE D'U02 EN RAPPORT AVEC LE STOCKAGE PERMANENT DU COMBUSTIBLE NUCLtAIRE US9 par S. Sunder et D.W. Shoesmith R9SUM9 Dans ce rapport, on examine la chimie de la dissolution de l'U02 dans des conditions se rapportant au stockage permanent du combustible nucleaire us6 dans une enceinte construite en formation g~ologique. Il permet la con- naissance chimique necessaire pour selectionner le modele le plus approprie de calcul de la vitesse de dissolution du combustible d'UO2 dans une en- ceinte de stockage permanent de dechets nucleaires. 11 decrit brievement la structure a l'etat solide de divers oxydes d'uranium; il examine la nature et le mecanisme de l'oxydation et de la dissolution de VUO2 dans les eaux