DOCSLIB.ORG

Unit 5 Page 9 Covalent Naming Worksheet

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Unit 5 Page 9 Covalent Naming Worksheet Unit 5 Page 9 Covalent Naming Worksheet Name the compound CO2 Carbon dioxide N2O Dinitrogen monoxide NI3 Nitrogen triodide As2O5 Diarsenic pentaoxide CO Carbon monoxide N2O3 Dinitrogen trioxide SiBr4 Silcon tetrabromide Cl2S7 Dichlorine heptasulfide PCl5 Phosphorus pentachloride B2Cl4 Diboron tetrachloride SF6 Sulfur hexafluoride P4O10 Tetraphosphorus decaoxide Give the formula for each compound nitrogen dioxide phosphorus trifluoride NO2 PF3 sulfur hexabromide dibromine heptaoxide SBr6 Br2O7 carbon diselenide dinitrogen tetrasulfide CSe2 N2S4 diphosphorus trioxide xenon hexafluoride P2O3 XeF6 silicon tetrachloride arsenic pentafluoride SiCl4 AsF5 1 Page 10 Practice Ionic Tin (II) Chloride PbCl2 SnCl2 Lead (II) Chloride Iron (III) Nitride Co2O3 FeN Cobalt (III) Oxide Copper (I) Bromide SnS CuBr Tin(II) Sulfide Circle the correct chemical formula for each compound below. Make sure the positive and negative charges are balanced. o calcium oxide CaO Ca2O CaO2 o magnesium fluoride MgF Mg2F MgF2 o sodium sulfide NaS Na2S NaS2 o barium nitride BaN Ba2N3 Ba3N2 Naming Acids If the compound begins with Hydrogen, it is an acid. If the acid does not contain a polyatomic ion, write the prefix hydro-, then name the second element and change the ending to –ic.’ o HCl hydrochloric acid o HBr hydrobromic acid o H2S hydrosulfuric acid Naming Acids with Polyatomic Ions The polyatomic ions you have memorized have –ate as the ending, so you name the polyatomic ion and change the ending to –ic. 2- Use sulfate (SO4 ) as the example H2SO4 is sulfuric acid 2- If the ion has one more oxygen atom than the base Persulfate (SO5 ), then the ion is named by adding the prefix per- and the suffix –ic o H2SO5 is persulfuric acid 2- If the ion has one less oxygen atom than the base Sulfite (SO3 ), then the ion is named with the suffix –ous. 2 o H2SO3 is sulfurous acid 2- If the ion has two less oxygen atoms than the base Hyposulfite (SO2 ), then the ion is named with the prefix hypo- and the suffix –ous. o H2SO2 is hyposulfurous acid Name the following: H2CO3 H3PO2 Cabonic acid Hypophosphorous acid HClO4 H3PO3 Perchloric acid Phosphorous acid 3 Page 11 Ionic Naming Worksheet 2 Fill in the table below with the correct ionic formula. Write the name of the compound in the box as well. The first one has been done for you as an example. Don’t forget that certain cations use Roman numerals in their names. Cl– O-2 N-3 + NaCl Na2O Na Na3N sodium chloride Sodium oxide Sodium Nitride Cu2O CuCl Cu3N Cu+ Copper (I) oxide Copper (I) Chloride Copper (I) Nitride CuCl2 Cu3N2 CuO Copper (II) Chloride Copper (II) nitride Cu+2 Copper (II) oxide MgO MgCl2 Mg3N2 Mg+2 Magnesium Oxide Magnesium Chloride Magnesium nitride Al2O3 AlCl3 Al N Al+3 Aluminum Oxide Aluminum Chloride Aluminum nitride Fe2O3 FeCl3 FeN Fe+3 Iron (III) oxide Iron (III) Chloride Iron (III) nitride CdO CdCl2 Cd3N2 Cd+2 Cadmium oxide Cadmium chloride Cadmium nitride 4 Page 12 Ionic Naming Worksheet 3 I. Write the formula for each of the compounds. 1) Copper (II) sulfate CuSO4 10) barium hydroxide Ba(OH)2 2) Ammonium nitrate NH4NO3 11) calcium chlorate Ca(ClO3)2 3) Lithium chloride LiCl 12) aluminum sulfite Al2(SO3)3 4) Magnesium acetate Mg(C2H3O2)2 13) chromium(II) oxide CrO 5) Sodium bromide NaBr 14) potassium iodide KI 6) Chromium (II) hydroxide Cr(OH)2 15) sodium hypochlorite NaClO 7) Lead (II) sulfate PbSO4 16) ammonium oxide (NH4)2O 8) Tin (IV) phosphate Sn3(PO4)4 17) potassium sulfide K2S 9) Sodium bicarbonate NaHCO3 18) lithium perchlorate LiClO4 II. Give the name of the following compounds. 1) Fe2(SO4)3 Iron (III) sulfate 10) Ag2SO4 Silver sulfate 2) Na3PO4 Sodium phosphate 11) Co(OH)2 Cobalt Hydroxide 3) Pb(NO3)2 Lead (II) Nitrate 12) AgClO3 Silver Chlorate 4) FeCl3 Iron (III) Chloride 13) K2SO3 Potassium Sulfite 5) KIO3 Potassium Iodate 14) CrCO3 Chromium Carbonate 6) CaF2 Calcium fluoride 15) K2CO3 Potassium Carbonate 7) Na2SO4 Sodium Sulfate 16) CaO Calcium Oxide 8) CuSO3 Copper (II) Sulfite 17) ZnCO3 Zinc Carbonate 9) PbF2 Lead (II) Fluoride 18) CuS Copper (II) Sulfide 5 Page 13 Acid Naming Worksheet 4 Complete the table by providing the name of formula for the following acids. 1. HNO3 Nitric acid 2. HCl Hydrochloric acid 3. H2SO4 Sulfuric acid 4. H2SO3 Sulfurous acid 5. HC2H3O2 Acetic acid 6. HBr Hydrobromic acid 7. HNO2 Nitrous acid 8. H3PO4 Phosphoric acid 9. H2S Hydrosulfuric acid 10. H2CO3 Carbonic acid 11. HI Hydroiodic acid 12. HF Hydrofluoric acid 13. HClO3 Chloric acid 14. HClO hypochlorous acid 15. H3PO3 Phosphorous acid H2SO4 16. Sulfuric Acid HNO3 17. Nitric Acid HCl 18. Hydrochloric Acid HC2H3O2 19. Acetic Acid HF 20. Hydrofluoric Acid HClO 21. Hypochlorous Acid H3PO3 22. Phosphorous Acid HNO2 23. Nitrous Acid H2CO3 24. Carbonic Acid H2S 25. Hydrosulfuric Acid 6 Page 14 Extra Practice Naming Worksheet 5 Formulas to Names 13. Calcium Hydroxide Ca(OH)2 1. KCN potassium cyanide 14. Aluminum Sulfide Al2S3 2. HNO3 Nitric acid 15. Silver Acetate Ag(C2H3O2)2 3. MgSO3 Magnesium sulfate 16. nitric acid HNO3 4. MnPO5 Manganese Perphosphate 17. Technetium (VI) Oxide TcO3 5. SiO4 Silcon tetraoxide 18. Chlorine difluorine ClF2 6. CuS Copper (II) Sulfide 19. Carbon monoxide CO 7. P4O10 Tetraphosphorus decaoxide 20. Zinc perphosphate Zn3 (PO5)2 8. Ni(HCO3)2 Nickel bicarbonate 21. Ammonium Nitrite NH4NO2 9. LiOH Lithium Hydroxide 22. Phosphoric Acid H3PO4 10. MgSO2 Magnesium hyposulfite 23. Hydronitric acid H3N 11. HNO2 Nitrous acid 24. Carbonous Acid H2CO2 12. HCl Hydrochloric acid 25. Strontium nitrite Sr(NO2)2 7 .
Load more

Recommended publications
  • Landolt-Börnstein Indexes of Organic Compounds Subvolumes A-I by V
    Landolt-Börnstein Indexes of Organic Compounds Subvolumes A-I By V. Vill, C. Bauhofer, G. Peters, H. Sajus, P. Weigner, LCI-Publisher and Chemistry Department of the University of Hamburg All printed index material has been used to build up the comprehensive Scidex database index developed by LCI Publisher GmbH, Hamburg For further information please visit www.lci-publisher.com From this database a CD-ROM and two online versions were derived. The first is attached to each of the printed subvolumes and the latter are offered for free use at the following addresses: Scidex Database online with graphical structure search on http://lb.chemie.uni-hamburg.de/ Or the easy to use html version on http://lb.chemie.uni-hamburg.de/static/ Landolt-Börnstein Numerical Data and Functional Relationships in Science and Technology New Series / Editor in Chief: W. Martienssen Index of Organic Compounds Subvolume A Compounds with 1 to 7 Carbon Atoms Editor: V. Vill Authors: V. Vill, G. Peters, H. Sajus 1 3 ISBN 3-540-66203-0 Springer-Verlag Berlin Heidelberg New York Library of Congress Cataloging in Publication Data Zahlenwerte und Funktionen aus Naturwissenschaften und Technik, Neue Serie Editor in Chief: W. Martienssen Index of Organic Compounds A: Editor: V. Vill At head of title: Landolt-Börnstein. Added t.p.: Numerical data and functional relationships in science and technology. Tables chiefly in English. Intended to supersede the Physikalisch-chemische Tabellen by H. Landolt and R. Börnstein of which the 6th ed. began publication in 1950 under title: Zahlenwerte und Funktionen aus Physik, Chemie, Astronomie, Geophysik und Technik.
    [Show full text]
  • CHEM 1411 Nomenclature Homework - Answers Part I
    1 CHEM 1411 Nomenclature Homework - Answers Part I 1. The following are a list of binary and pseudobinary ionic compounds. Write the name when the formula is given. Write the formula when the name is given. (a) AlCl3 aluminum chloride (k) rubidium oxide Rb2O (b) AuBr3 gold (III) bromide (l) chromium (III) selenide Cr2Se3 (c) Na2S sodium sulfide (m) barium iodide BaI2 (d) Cu3P2 copper (II) phosphide (n) copper (I) fluoride CuF (e) Fe(OH)2 iron (II) hydroxide (o) copper (II) fluoride CuF2 (f) NH4OH ammonium hydroxide (p) strontium cyanide Sr(CN)2 (g) Co(CH3COO)3 cobalt (III) acetate (q) mercury (II) bromide HgBr2 (h) Zn(SCN)2 zinc thiocyanate (r) mercury (I) bromide Hg2Br2 (i) CaCrO4 calcium chromate (s) magnesium permanganate Mg(MnO4)2 (j) K2Cr2O7 potassium dichromate (t) lithium nitride Li3N 2. The following are lists of covalent compounds. Write the name when a formula is given. Write the formula when given a name. (a) CSe2 carbon diselenide (h) dichlorine heptoxide Cl2O7 (b) SF6 sulfur hexafluoride (i) xenon tetrafluoride XeF4 (c) BrF5 bromine pentafluoride (j) carbon monoxide CO (d) P4O10 tetraphosphorous decoxide (k) oxygen O2 (e) Cl2O dichlorine oxide (l) diboron trioxide B2B O3 (f) NH3 ammonia (m) arsenic trifluoride AsF3 (g) N2 dinitrogen or nitrogen (n) diiodine I2 2 3. The following are lists of acids or acid-forming compounds. Write the name when the formula is given. Write the formula when the name is given. (a) H3PO2 hypophosphorous acid (k) hydrogen cyanide HCN (g) (b) H2SO4 sulfuric acid (l) periodic acid HIO4 (c) HClO hypochlorous acid (m) hypochlorous acid HClO (d) H3PO4 phosphoric acid (n) nitric acid HNO3 (e) HBrO4 perbromic acid (o) acetic acid CH3CO2H (f) HIO2 iodous acid (p) chloric acid HClO3 (g) HI (g) hydrogen iodide (q) perbromic acid HBrO4 (h) HI (aq) hydroiodic acid (r) hydrofluoric acid HF (aq) (i) HCN (aq) hydrocyanic acid (s) phosphorous acid H3PO3 (j) HBrO hypobromous acid (t) hydrosulfuric acid H2S (aq) 4.
    [Show full text]
  • Full Compositional Control of Pbs X Se 1− X Thin Films by the Use Of
    Dalton Transactions View Article Online PAPER View Journal | View Issue Full compositional control of PbSxSe1−x thin films by the use of acylchalcogourato lead(II) complexes Cite this: Dalton Trans., 2018, 47, 16938 as precursors for AACVD† Tagbo Emmanuel Ezenwa,a Paul D. McNaughter, *a James Raftery,a David J. Lewis a and Paul O’Brien *a,b Selenium and sulfur derivatives of lead(II) acylchalcogourato complexes have been used to deposit PbSxSe1−x thin films by AACVD. By variation of the mole ratio of sulfur and selenium precursors in the aerosol feed solution the full range of compositions of PbSxSe1−x was obtained, i.e. 0 ≥ x ≥ 1. The films Received 23rd August 2018, showed no contaminant phases demonstrating the potential for acylchalcogourato metal complexes as Accepted 26th September 2018 precursors for metal chalcogenide thin films. The crystal structure for bis[N,N-diethyl-N’-2- DOI: 10.1039/c8dt03443e naphthoylthioureato]lead(II) was solved and displayed the expected decreases in Pb–E bond lengths from rsc.li/dalton the previously reported selenium variant. Creative Commons Attribution 3.0 Unported Licence. – Introduction xanthates16 21 There are fewer reports on the use of single source precursors forming lead selenides due to the synthesis of Lead chalcogenide nanomaterials have potential within photo- noxious carbon diselenide when synthesising dithiocarbamates voltaic devices due to their advantageous bulk bandgaps in the and xanthates. N-Acyl chalcogoureas offer a convenient route to infra-red region (PbS = 0.41 eV, PbSe = 0.28 eV and PbTe = 0.31 acarbon–chalcogen double bond due to the availability and ease eV) and the ability to tune the band gap by quantum confine- of the use of potassium selenocyanate and potassium thio- This article is licensed under a ment.
    [Show full text]
  • Carbon Dioxide - Wikipedia
    5/20/2020 Carbon dioxide - Wikipedia Carbon dioxide Carbon dioxide (chemical formula CO2) is a colorless gas with Carbon dioxide a density about 60% higher than that of dry air. Carbon dioxide consists of a carbon atom covalently double bonded to two oxygen atoms. It occurs naturally in Earth's atmosphere as a trace gas. The current concentration is about 0.04% (412 ppm) by volume, having risen from pre-industrial levels of 280 ppm.[8] Natural sources include volcanoes, hot springs and geysers, and it is freed from carbonate rocks by dissolution in water and acids. Because carbon dioxide is soluble in water, it occurs naturally in groundwater, rivers and lakes, ice caps, glaciers and seawater. It is present in deposits of petroleum and natural gas. Carbon dioxide is odorless at normally encountered concentrations, but at high concentrations, it has a sharp and acidic odor.[1] At such Names concentrations it generates the taste of soda water in the Other names [9] mouth. Carbonic acid gas As the source of available carbon in the carbon cycle, atmospheric Carbonic anhydride carbon dioxide is the primary carbon source for life on Earth and Carbonic oxide its concentration in Earth's pre-industrial atmosphere since late Carbon oxide in the Precambrian has been regulated by photosynthetic organisms and geological phenomena. Plants, algae and Carbon(IV) oxide cyanobacteria use light energy to photosynthesize carbohydrate Dry ice (solid phase) from carbon dioxide and water, with oxygen produced as a waste Identifiers product.[10] CAS Number 124-38-9 (http://ww w.commonchemistr CO2 is produced by all aerobic organisms when they metabolize carbohydrates and lipids to produce energy by respiration.[11] It is y.org/ChemicalDeta returned to water via the gills of fish and to the air via the lungs of il.aspx?ref=124-38- air-breathing land animals, including humans.
    [Show full text]
  • Proceedings of the Indiana Academy of Science
    : Organic Compounds op Selenium 165 I. ORGANIC COMPOUNDS OF SELENIUM W. E. Bradt and M. Van Valkenhurgh, University of Cincinnati Introduction. Because selenium and some of its compounds are now- available in considerable amounts at reasonable prices, the investigation of the preparation and properties of organic selenium compounds is quite feasible. In order to further this work, the senior author plans a series of papers which, when completed, will present: (a) a classification of the known organic selenium compounds based on the analogous oxygen and sulphur types, (b) a complete list of all known organic selenium compounds, (c) a resume of the chemistry and methods of preparation developed for each class of compounds, and (d) a com- plete bibliography for each known organic selenium compound. The physiological action of some of the more common inorganic selenium compounds is well known. Many organic selenium compounds are reported to exhibit valuable therapeutic and tinctorial properties. However, the investigation of these properties has been so incomplete that organic compounds of selenium are still only of scientific interest. It is hoped that a systematic presentation of the chemistry of organic selenium compounds, with a statement of the extent of the synthetic work accomplished to date, will create interest in developing the possibilities of service to mankind (dyes, medicinals etc.), which probably exist in this field. Investigation in this direction lends itself particularly to the worker who has available only limited equipment. The reactions can usually be conducted in apparatus which is always available or which may be easily prepared. Aliphatic Selenols In this group will be discussed compounds, represented by the following formulas, in which "R" is a methyl group, the hydrogen atoms of which may or may not be replaced by other groups.
    [Show full text]
  • Nuclear Magnetic Shielding Tensors for the Carbon, Nitrogen, and Selenium Nuclei of Selenocyanates — a Combined Experimental and Theoretical Approach
    Color profile: Disabled Composite Default screen 614 Nuclear magnetic shielding tensors for the carbon, nitrogen, and selenium nuclei of selenocyanates — a combined experimental and theoretical approach Guy M. Bernard, Klaus Eichele, Gang Wu, Christopher W. Kirby, and Roderick E. Wasylishen Abstract: The principal components of the carbon, nitrogen, and selenium chemical shift (CS) tensors for several solid selenocyanate salts have been determined by NMR measurements on stationary or slow magic-angle-spinning powder samples. Within experimental error, all three CS tensors are axially symmetric, consistent with the expected linear geometry of these anions. The spans (Ω) of the carbon and selenium CS tensors for the selenocyanate anion (SeCN–) are approximately 300 and 800 ppm, respectively, much less than the corresponding values for carbon diselenide (CSe2). This difference is a consequence of the difference in the CS tensor components perpendicular to the C∞ sym- metry axes in these systems. Ab initio calculations show that the orbital symmetries of these compounds are a signifi- σ π cant factor in the shielding. For CSe2, efficient mixing of the and orbitals results in a large paramagnetic contribution to the total shielding of the chemical shielding tensor components perpendicular to the molecular axis. Such mixing is less efficient for the SeCN–, resulting in a smaller paramagnetic contribution and hence in greater shielding in directions perpendicular to the molecular axis. Key words: selenocyanates, solid-state NMR, carbon shielding tensors, nitrogen shielding tensors, selenium shielding tensors, ab initio calculations. Résumé : À partir de mesures RMN sur des échantillons de poudre stationnaires ou à rotation lente à l’angle magique de plusieurs sélénocyanates solides, on en a déterminé les principaux composant des tenseurs des déplacements chimiques (DC) du carbone, de l’azote et du sélénium.
    [Show full text]
  • Sorption Studies of Synthetically Modified Carbon Nanomaterials
    Sorption Studies of Synthetically Modified Carbon Nanomaterials A Thesis Submitted to the College of Graduate Studies and Research In Partial Fulfillment of the Requirements For the Degree of Doctor of Philosophy In the Department of Chemistry University of Saskatchewan Saskatoon By Jae Hyuck Kwon Copyright Jae Hyuck Kwon, January 2014. All rights reserved. PERMISSION TO USE In presenting this thesis in partial fulfilment of the requirements for a Postgraduate degree from the University of Saskatchewan, I agree that the Libraries of this University may make it freely available for inspection. I further agree that permission for copying of this thesis in any manner, in whole or in part, for scholarly purposes may be granted by the professor or professors who supervised my thesis work or, in their absence, by the Head of the Department or the Dean of the College in which my thesis work was done. It is understood that any copying or publication or use of this thesis or parts thereof for financial gain shall not be allowed without my written permission. It is also understood that due recognition shall be given to me and to the University of Saskatchewan in any scholarly use which may be made of any material in my thesis. Requests for permission to copy or to make other use of material in this thesis in whole or part should be addressed to: Head of the Department of Chemistry University of Saskatchewan Saskatoon, Saskatchewan, S7N 5C9 i DEDICATION I would like to dedicate this dissertation and its all related honour to my wife, Gloria.
    [Show full text]
  • Influence of Selenium Biofortification on the Growth and Bioactive
    foods Article Influence of Selenium Biofortification on the Growth and Bioactive Metabolites of Ganoderma lucidum Mengmeng Xu 1,2, Song Zhu 3, Lingling Wang 1, Zhiyi Wei 1,2, Liting Zhao 1,2, Guiyang Shi 1,2,4 and Zhongyang Ding 1,2,4,* 1 Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education & School of Biotechnology, Jiangnan University, Wuxi 214122, China; [email protected] (M.X.); [email protected] (L.W.); [email protected] (Z.W.); [email protected] (L.Z.); [email protected] (G.S.) 2 National Engineering Laboratory for Cereal Fermentation Technology, Jiangnan University, Wuxi 214122, China 3 State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi 214122, China; [email protected] 4 Jiangsu Provincial Research Center for Bioactive Product Processing Technology, Jiangnan University, Wuxi 214122, China * Correspondence: [email protected]; Tel./Fax: +86-510-85918221 Abstract: Selenium biofortification of edible and medicinal mushrooms is an effective way to produce selenium-enriched food supplements. Ganoderma lucidum is the typical one with excellent biological activity. This study investigated G. lucidum growth and bioactive metabolites alterations during liquid culture with different concentrations of selenite. Low selenium levels did not affect growth and mycelia morphology, whereas high selenium levels negatively influenced growth, dramatically decreased biomass, caused nucleic acid and protein leakage, damaged cell walls and membranes, and resulted in indicators such as degraded cells, a red color, and an unpleasant odor. Through headspace-solid phase microextraction-gas chromatography-mass spectrometry (HS-SPME-GC-MS) Citation: Xu, M.; Zhu, S.; Wang, L.; analysis, ten volatile Se compounds were identified in G.
    [Show full text]
  • One-Pot Synthesis of Heterocycle-Fused 1,3-Diselenole
    ORGANIC LETTERS 1999 One-Pot Synthesis of Heterocycle-Fused Vol. 1, No. 1 1,3-Diselenole-2-selones as the Key 23-25 Precursors of Tetraselenafulvalene-Type Electron Donors Atsushi Morikami, Kazuo Takimiya, Yoshio Aso,† and Tetsuo Otsubo* Department of Applied Chemistry, Faculty of Engineering, Hiroshima UniVersity, Kagamiyama 1-4-1, Higashi-Hiroshima 739-8527, Japan [email protected] Received March 14, 1999 ABSTRACT A simple one-pot synthetic method of a series of 4,5-alkylenedichalcogeno-substituted 1,3-diselenole-2-selones by successive treatments of trimethylsilylacetylene with butyllithium, selenium, carbon diselenide, and finally r,ω-bis(chalcogenocyanato)alkanes is described. Since the discovery of a number of organic superconductors generally inaccessible and have been obtained by only limited based on BEDT-TTF,1 analogous heterocycle-fused TTF- methods.5 The heterocycle-fused 1,3-diselenole-2-selones (2) type donors have been systematically studied with the and the corresponding ketones are very important as the key purpose of searching for new organic superconductors with precursors of 1, and accordingly the ready synthetic methods high Tc.2 In particular, the TSF variants such as 1 have of these compounds are highly desirable. We now would attracted considerable interest,3 because the introduced like to report a simple one-pot synthesis of 2, together with selenium atoms can contribute to an increase of intermo- 4,5-bis(methylthio)-1,3-diselenole-2-selone (3), from com- lecular interactions.4 However, when compared with the TTF- mercially available trimethylsilylacetylene (Figure 1). type donors, such heterocycle-fused TSF-type donors are † Institute for Fundamental Research of Organic Chemistry, Kyushu University.
    [Show full text]
  • Mapping the Drivers of Uncertainty in Atmospheric Selenium Deposition
    Mapping the drivers of uncertainty in atmospheric selenium deposition with global sensitivity analysis Aryeh Feinberg, Maliki Moustapha, Andrea Stenke, Bruno Sudret, Thomas Peter, Lenny Winkel To cite this version: Aryeh Feinberg, Maliki Moustapha, Andrea Stenke, Bruno Sudret, Thomas Peter, et al.. Mapping the drivers of uncertainty in atmospheric selenium deposition with global sensitivity analysis. Atmospheric Chemistry and Physics Discussions, European Geosciences Union, In press, pp.1-42. 10.5194/acp- 2019-787. hal-02305475 HAL Id: hal-02305475 https://hal.archives-ouvertes.fr/hal-02305475 Submitted on 4 Oct 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. MAPPING THE DRIVERS OF UNCERTAINTY IN ATMOSPHERIC SELENIUM DEPOSITION WITH GLOBAL SENSITIVITY ANALYSIS A. Feinberg, M. Moustapha, A. Stenke, B. Sudret, T. Peter L. Winkel CHAIR OF RISK,SAFETY AND UNCERTAINTY QUANTIFICATION Risk, Safety & STEFANO-FRANSCINI-PLATZ 5 Uncertainty Quantification CH-8093 ZURICH¨ Data Sheet Journal: Atmospheric Chemistry and Physics Report Ref.: RSUQ-2019-003 Arxiv Ref.: - DOI: https://doi.org/10.5194/acp-2019-787 Date submitted: September 11, 2019 Date accepted: Mapping the drivers of uncertainty in atmospheric selenium deposition with global sensitivity analysis Aryeh Feinberg1,2,3, Moustapha Maliki4, Andrea Stenke1, Bruno Sudret4, Thomas Peter1, and Lenny H.
    [Show full text]
  • Organometallic Chemistry
    Advances in Organometallic Chemistry EDITED BY ROBERT WEST ANTHONY F. HILL DEPARTMENT OF CHEMISTRY DEPARTMENT OF CHEMISTRY UNIVERSITY OF WISCONSIN IMPERIAL COLLEGE OF SCIENCE, MADISON, WISCONSIN TECHNOLOGY, AND MEDICINE LONDON, ENGLAND FOUNDING EDITOR F. GORDON A. STONE VOLUME 45 Cumulative Subject and Contributor Indexes and Tables of Contents for Volumes 1-44 ACADEMIC PRESS San Diego London Boston New York Sydney Tokyo Toronto This book is printed on acid-Cree paper. @ Copyright 'C 2000 hy ACADEMIC PRESS All Rights Reserved. No part ufthis publication may bc reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy. recording, or any information storage and retrieval system, without permission in writing from thc Publisher. The appearaiicc ofthe code at the bottom ofthe lirst page of a chaptcr in this book indicates the Publisher's consent that copies of the chapter may he made for personal or internal use of specific clients. This consent is given on the condition, however, that the copier pay the stated per copy fee through the Copyright Clearance Center, Inc. (222 Rosewood Drive, Danvers, Massachusetts 01 923). for copying beyond that permitted by Sections 107 or 108 of the 1J.S. Copyright Law. This consent does not extend to other kinds of copying, such as copying for general distribution, for advertising or promotional purposes, for creating new collective works. or for resale. Copy fees for pre-2000 chapters are as shown on the title pages. Ifno fee code appears on the title page, the copy fee is the same as for current chaptcrs. no~1s-30~5/oo$30.00 Explicit permission from Academic Press is not required to reproduce a maximum of two figures or tables from an Academic Press chapter in another scientific or research publication provided that the material has not been credited to another source and that full credit to the Academic Press chapter is given.
    [Show full text]
  • Assessing the Chemistry and Bioavailability of Dissolved Organic Matter from Glaciers and Rock 2 Glaciers 3
    bioRxiv preprint doi: https://doi.org/10.1101/115808; this version posted April 11, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 ASSESSING THE CHEMISTRY AND BIOAVAILABILITY OF DISSOLVED ORGANIC MATTER FROM GLACIERS AND ROCK 2 GLACIERS 3 4 1,2 1,3 3 1,4 5 Fegel, Timothy , Boot, Claudia M. , Broeckling, Corey D. , Hall, Ed K. 6 1. Natural Resource Ecology Laboratory, Colorado State University 2. U.S. Forest Service, 7 Rocky Mountain Research Station, 3. Department of Chemistry, Colorado State University 4. 8 Proteomics and Metabolomics Facility, Colorado State University 4. Department of Ecosystem 9 Science and Sustainability, Colorado State University 10 11 Tim Fegel [email protected] 12 13 14 Key Points: 15 Bioavailability of organic matter released from glaciers is greater than that of rock glaciers in the 16 Rocky Mountains. 17 The use of GC-MS for ecosystem metabolomics represents a novel approach for examining 18 complex organic matter pools. 19 Both glaciers and rock glaciers supply highly bioavailable sources of organic matter to alpine 20 headwaters in Colorado. 1 bioRxiv preprint doi: https://doi.org/10.1101/115808; this version posted April 11, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license.
    [Show full text]