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Brief Guide to the Nomenclature of Organic Chemistry
1 Brief Guide to the Nomenclature of Table 1: Components of the substitutive name Organic Chemistry (4S,5E)-4,6-dichlorohept-5-en-2-one for K.-H. Hellwich (Germany), R. M. Hartshorn (New Zealand), CH3 Cl O A. Yerin (Russia), T. Damhus (Denmark), A. T. Hutton (South 4 2 Africa). E-mail: [email protected] Sponsoring body: Cl 6 CH 5 3 IUPAC Division of Chemical Nomenclature and Structure suffix for principal hept(a) parent (heptane) one Representation. characteristic group en(e) unsaturation ending chloro substituent prefix 1 INTRODUCTION di multiplicative prefix S E stereodescriptors CHEMISTRY The universal adoption of an agreed nomenclature is a key tool for 2 4 5 6 locants ( ) enclosing marks efficient communication in the chemical sciences, in industry and Multiplicative prefixes (Table 2) are used when more than one for regulations associated with import/export or health and safety. fragment of a particular kind is present in a structure. Which kind of REPRESENTATION The International Union of Pure and Applied Chemistry (IUPAC) multiplicative prefix is used depends on the complexity of the provides recommendations on many aspects of nomenclature.1 The APPLIED corresponding fragment – e.g. trichloro, but tris(chloromethyl). basics of organic nomenclature are summarized here, and there are companion documents on the nomenclature of inorganic2 and Table 2: Multiplicative prefixes for simple/complicated entities polymer3 chemistry, with hyperlinks to original documents. An No. Simple Complicated No. Simple Complicated AND overall -
Minutes of the IUPAC Chemical Nomenclature and Structure Representation Division (VIII) Committee Meeting Boston, MA, USA, August 18, 2002
Minutes of the IUPAC Chemical Nomenclature and Structure Representation Division (VIII) Committee Meeting Boston, MA, USA, August 18, 2002 Members Present: Dr Stephen Heller, Prof Herbert Kaesz, Prof Dr Alexander Lawson, Prof G. Jeffrey Leigh, Dr Alan McNaught (President), Dr. Gerard Moss, Prof Bruce Novak, Dr Warren Powell (Secretary), Dr William Town, Dr Antony Williams Members Absent: Dr. Michael Dennis, Prof Michael Hess National representatives Present: Prof Roberto de Barros Faria (Brazil) The second meeting of the Division Committee of the IUPAC Division of Chemical Nomenclature and Structure Representation held in the Great Republic Room of the Westin Hotel in Boston, Massachusetts, USA was convened by President Alan McNaught at 9:00 a.m. on Sunday, August 18, 2002. 1.0 President McNaught welcomed the members to this meeting in Boston and offered a special welcome to the National Representative from Brazil, Prof Roberto de Barros Faria. He also noted that Dr Michael Dennis and Prof Michael Hess were unable to be with us. Each of the attendees introduced himself and provided a brief bit of background information. Housekeeping details regarding breaks and lunch were announced and an invitation to a reception from the U. S. National Committee for IUPAC on Tuesday, August 20 was noted. 2.0 The agenda as circulated was approved with the addition of a report from Dr Moss on the activity on his website. 3.0 The minutes of the Division Committee Meeting in Cambridge, UK, January 25, 2002 as posted on the Webboard (http://www.rsc.org/IUPAC8/attachments/MinutesDivCommJan2002.rtf and http://www.rsc.org/IUPAC8/attachments/MinutesDivCommJan2002.pdf) were approved with the following corrections: 3.1 The name Dr Gerard Moss should be added to the members present listing. -
Ethylene Glycol
Ethylene glycol Ethylene glycol (IUPAC name: ethane-1,2-diol) is an organic Ethylene glycol compound with the formula (CH2OH)2. It is mainly used for two purposes, as a raw material in the manufacture of polyester fibers and for antifreeze formulations. It is an odorless, colorless, sweet-tasting, viscous liquid. Contents Production Industrial routes Biological routes Historical routes Uses Coolant and heat-transfer agent Antifreeze Precursor to polymers Other uses Dehydrating agent Hydrate inhibition Applications Chemical reactions Toxicity Environmental effects Names Notes Preferred IUPAC name References Ethane-1,2-diol External links Other names Ethylene glycol 1,2-Ethanediol Production Ethylene alcohol Hypodicarbonous acid Monoethylene glycol Industrial routes 1,2-Dihydroxyethane Ethylene glycol is produced from ethylene (ethene), via the Identifiers intermediate ethylene oxide. Ethylene oxide reacts with water to CAS Number 107-21-1 (http produce ethylene glycol according to the chemical equation: s://commonche mistry.cas.org/d C2H4O + H2O → HO−CH2CH2−OH etail?cas_rn=10 7-21-1) 3D model (JSmol) Interactive This reaction can be catalyzed by either acids or bases, or can occur image (https://ch at neutral pH under elevated temperatures. The highest yields of emapps.stolaf.e ethylene glycol occur at acidic or neutral pH with a large excess of du/jmol/jmol.ph water. Under these conditions, ethylene glycol yields of 90% can be p?model=OCC achieved. The major byproducts are the oligomers diethylene glycol, O) triethylene glycol, and tetraethylene glycol. The separation of these oligomers and water is energy-intensive. About 6.7 million tonnes 3DMet B00278 (http://w are produced annually.[4] ww.3dmet.dna.af frc.go.jp/cgi/sho A higher selectivity is achieved by use of Shell's OMEGA process. -
Source-Based Nomenclature for Single-Strand Homopolymers and Copolymers (IUPAC Recommendations 2016)
Pure Appl. Chem. 2016; 88(10-11): 1073–1100 IUPAC Recommendations Richard G. Jones*, Tatsuki Kitayama*, Karl-Heinz Hellwich, Michael Hess, Aubrey D. Jenkins, Jaroslav Kahovec, Pavel Kratochvíl, Itaru Mita†, Werner Mormann, Christopher K. Ober, Stanisław Penczek, Robert F. T. Stepto†, Kevin Thurlow, Jiří Vohlídal and Edward S. Wilks Source-based nomenclature for single-strand homopolymers and copolymers (IUPAC Recommendations 2016) DOI 10.1515/pac-2015-0702 Received July 10, 2015; accepted June 27, 2016 Abstract: IUPAC recommendations on source-based nomenclature for single-strand polymers have so far addressed its application mainly to copolymers, non-linear polymers and polymer assemblies, and within generic source-based nomenclature of polymers. In this document, rules are formulated for devising a satis- factory source-based name for a polymer, whether homopolymer or copolymer, which are as clear and rigor- ous as possible. Thus, the source-based system for naming polymers is presented in a totality that serves as a user-friendly alternative to the structure-based system of polymer nomenclature. In addition, because of their widespread and established use, recommendations for the use of traditional names of polymers are also elaborated. Keywords: apparent monomer; copolymer; end-groups; homopolymer; IUPAC; IUPAC nomenclature; monomer; nomenclature; polymers; polymer nomenclature; source-based names; traditional names. Dedicated to: The memory of Robert (Bob) Stepto, former president of the Polymer Division of IUPAC, whose recent death denied him the satisfaction of witnessing the publication of this manuscript on which he expended much effort. Article note: Sponsoring bodies: IUPAC Division of Chemical Nomenclature and Structure Representation and IUPAC Polymer Division, Sub-Committee on Polymer Terminology: see more details on p. -
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. -
Advantages of Nodal Numbering for Uniquely Identifying Atoms in Chemical Nomenclature Alan L
CROATICA CHEMICA ACTA CCACAA 59 (3) 547-563 (198G)1 YU ISSN 0011-1643 CCA-1668 UDC 541 Original Scientific Paper Advantages of Nodal Numbering for Uniquely Identifying Atoms in Chemical Nomenclature Alan L. Goodson 1060 Woodmere Road, CoLumbus, Ohio 43220, U.S.A. and Noel Lozac'h Institut des Sciences de la Matiere et du Rayonnement, Universite de Caen, 14032 Caen Cedex, France Received September 2, 1985 There are situations in chemical nomenclature where duplica- tion of locants creates difficulties (a) in describing modifications to chemical structures, (b) in describing stereochemistry, (c) in identifying isotopically-labeled atoms, and (d) in uniquely iden- tifying atoms for crystallography, Nodal nomenclature is shown to avoid these problems and to simplify such descriptions. INTRODUCTION The first concerted international agreements on chemical nornenclature- were made in Geneva in 18921. From these agreements has aris en the Inter- national Union of Pure and Applied Chemistry (IUPAC), as we know it today. IUPAC has, in general, »confined its efforts to codifying sound practices. which already existed-". IUPAC has published a set of internationally-agreed rules of organic chemistry", However, more than one sound practice is some- times described (e. g., for naming organic compounds containing phosphorus,. arsenic, antimony or bismuth) without any indication of which practice is preferred. For practical reasons, indexers of chemical literature, such as Chemical Abstracts Service and Beilstein, must be more selective, i. e. more systematic, than IUP AC and must even develop their own rules when IUP AC rules are vague or non-existent. The rules published by IUP AC include the powerful and commonly-used technique of substitutive nomenclature. -
WO 2016/196440 Al 8 December 2016 (08.12.2016) 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 2016/196440 Al 8 December 2016 (08.12.2016) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every A61P 3/04 (2006.01) A61K 33/40 (2006.01) kind of national protection available): AE, AG, AL, AM, A61P 9/10 (2006.01) A61K 38/44 (2006.01) AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, A61K 35/74 (2015.01) A61K 31/17 (2006.01) BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (21) International Application Number: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, PCT/US20 16/034973 KZ, LA, LC, LK, LR, LS, LU, LY, MA, MD, ME, MG, (22) International Filing Date: MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, 3 1 May 2016 (3 1.05.2016) PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, (25) Filing Language: English TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (26) Publication Language: English (84) Designated States (unless otherwise indicated, for every (30) Priority Data: kind of regional protection available): ARIPO (BW, GH, 62/169,480 1 June 2015 (01 .06.2015) US GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, 62/327,283 25 April 2016 (25.04.2016) US TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, (71) Applicant: XENO BIOSCIENCES INC. -
Naming Compounds
Naming Compounds Naming compounds is an important part of chemistry. Most compounds fall in to one of three categories- ionic compounds, molecular compounds, or acids. Part One: Naming Ionic Compounds Identifying Ionic Compounds Ionic compounds consist of combinations of positively charged ions called cations (usually metals), and negatively charged ions called anions (usually non-metals). In general, you can identify an ionic compound because it contains a metal (these are usually found in the left and center areas of the periodic table) and a non-metal (these are generally found in the right hand area of the periodic table). Also, a compound will have no charge. For example, NaCl and Fe2O3 are ionic compounds; they each contain a metal (Na and Fe) and a non-metal (Cl - and O), and they do not have charges. MnO4 is NOT an ionic compound; it does contain a metal (Mn) and a non-metal (O), but it has a charge. Thus, it is a polyatomic ion, not a compound. A compound will NEVER have a charge! Naming Ionic Compounds There are three steps involved in naming ionic compounds- naming the cation, naming the anion, and naming the entire compound. 1. Name the cation. i. Cations formed from metal atoms have the same name as the metal. Examples: Na+= sodium ion; Al3+= aluminum ion ii. If a metal can form ions of different charges (i.e., is one of the central transition metals), specify the charge with Roman numerals in parentheses. Examples: Fe+= iron (I) ion; Fe2+= iron (II) ion; Fe3+= iron (III) ion iii. -
United States Patent Office Patented Mar
3,573,257 United States Patent Office Patented Mar. 30, 1971 2 3,573,257 to be used as the catalyst by treating said cupric salt PROCESS FOR PRODUCTION OF with an alkali phenolate to form a basic cupric salt. In POLYPHENY ENE OXDES this case, the alkali phenolate is not a polymerization Seizo Nakashio, Nishinomiya-shi, and Isamu Nakagawa, catalyst component. In the above-mentioned known proc Osaka, Japan, assignors to Sumitomo Chemical Com esses, amines including tertiary amines are always used pany, Ltd., Osaka, Japan 5 as one of the essential components of the catalyst, though No Drawing. Continuation-in-part of application Ser. No. 71,918, Mar. 11, 1968. This application Dec. 29, 1969, there is a difference in metallic compound. Therefore, it Ser. No. 888,915 is troublesome to prevent the resulting polymer from Claims priority, application Japan, Mar. 28, 1967, being colored. It is difficult in the well-known methods to 42/19,740 O obtain the desired products without these disadvantages. int. C. C08g 23/18 The polymers prepared by the known process, in which U.S. C. 260-47 13 Claims the amines were used in the reaction system, contain a small amount of nitrogen, and it was difficult to remove said nitrogen from the polymer by any conventional puri ABSTRACT OF THE DISCLOSUIRE 5 fication procedure in which the polymer molecules were not destroyed. The nitrogen residue surely originates from Polyphenylene oxide is produced by reacting oxygen the catalyst used and is evidently incorporated into the with a phenol compound represented by the following polymer molecules. -
Chemistry 2202 Curriculum Guide 2018
Chemistry 2202 Curriculum Guide 2018 MISSION STATEMENT Department of Education and Early Childhood Development Mission Statement The Department of Education and Early Childhood Development will improve provincial early childhood learning and the K-12 education system to further opportunities for the people of Newfoundland and Labrador. CHEMISTRY 2202 CURRICULUM GUIDE 2018 I II CHEMISTRY 2202 CURRICULUM GUIDE 2018 TABLE OF CONTENTS Table of Contents Acknowledgements ...................................................................................... v Section One: Newfoundland and Labrador Curriculum Outcomes Based Education........................................................................................1 Context for Teaching and Learning .............................................................................4 Inclusive Education..................................................................................................4 Literacy ..................................................................................................................10 Learning Skills for Generation Next .......................................................................12 Assessment and Evaluation ......................................................................................15 Section Two: Curriculum Design Rationale ...................................................................................................................19 Curriculum Outcomes Framework ............................................................................20 -
Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005)
NOMENCLATURE OF INORGANIC CHEMISTRY IUPAC Recommendations 2005 IUPAC Periodic Table of the Elements 118 1 2 21314151617 H He 3 4 5 6 7 8 9 10 Li Be B C N O F Ne 11 12 13 14 15 16 17 18 3456 78910 11 12 Na Mg Al Si P S Cl Ar 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 Rb Sr Y Zr Nb Mo Tc Ru Rh Pd Ag Cd In Sn Sb Te I Xe 55 56 * 57− 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 Cs Ba lanthanoids Hf Ta W Re Os Ir Pt Au Hg Tl Pb Bi Po At Rn 87 88 ‡ 89− 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 Fr Ra actinoids Rf Db Sg Bh Hs Mt Ds Rg Uub Uut Uuq Uup Uuh Uus Uuo * 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu ‡ 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 Ac Th Pa U Np Pu Am Cm Bk Cf Es Fm Md No Lr International Union of Pure and Applied Chemistry Nomenclature of Inorganic Chemistry IUPAC RECOMMENDATIONS 2005 Issued by the Division of Chemical Nomenclature and Structure Representation in collaboration with the Division of Inorganic Chemistry Prepared for publication by Neil G. -
Organic Nomenclature-IV.Pmd
Concepts in Chemistry CHAPTER-IV TRIVIAL OR COMMON SYSTEM OF NOMENCLATURE Naming an organic compound on the basis of the rules recommended by IUPAC is absolutely essential for big and complex molecules. However, small molecules are more popularly addressed by their common names or the trivial or the primitive names. We already know before that IUPAC has accepted a few common names as official names e.g acetic acid, formic acid etc. for some compounds and isopropyl, sec-butyl, tert-butyl etc. as some groups. A detailed logically genesis of the common system is discussed below. TYPES OF CARBON ATOMS: There are four types of carbon atoms. (i) Primary or 10 carbon atom: carbon atom attached with 3 or 4 H atoms. (ii) Secondary(sec-) or 20 carbon atom: carbon atom attached with 2 H atoms. (iii) Tertiary(tert-) or 30 carbon atom: carbon atom attached with 1 H atom (iv) Quaternary or 40 carbon atom: carbon atom attached with no H atom. 0 0 0 1 1 1 CH3 0 0 CH3 0 0 CH3 1 3 0 4 2 3 Example: H3CCH C CH2 CH 0 0 1 1 CH3 CH3 In the above example, all the carbon atoms have been assigned with their types. SAQ IV.1. (i)Name the molecule in which a primary carbon atoms is linked with 4 H atom. (ii)Draw the structure and give the IUPAC name of the compound which contains one 40 and four 10 carbon atoms. TYPES OF ALKYL GROUPS: In common system alkyl groups are prefixed with the symbols n-, iso, sec-, tert- and neo.