English for Chemists Vocabulary Brno 2014 Contents Sound Records. 4 English for Chemists. 5 Lesson 1. 5 Lesson 2. 7 Lesson 3. 9 Chemical Elements. 10 Nomenclature of Inorganic Compounds. 13 Ions. 13 Monatomic cations. 13 Monatomic anions. 13 Polyatomic ions. 13 Oxoanions of nitrogen, sulphur and chlorine. 14 Ionic compounds. 14 Binary molecular compounds. 14 Greek prefixes used in nomenclature. 15 Acids. 15 Nomenclature of Organic Compounds. 17 Nomenclature of Alkanes. 17 Nomenclature of Alkenes. 17 Nomenclature of Alkynes. 17 Derivatives of Benzene. 17 Functional Groups. 17 Carboxylic Acids. 17 Test 1. 18 Test 2. 18 General Chemistry. 19 Sound Records English for Chemists: Lesson 1 Lesson 2 Lesson 3 Chemical Elements Nomenclature of Inorganic Compounds Nomenclature of Organic Compounds General Chemistry English for Chemists Lesson 1 round flat-bottom flasks round-bottom flasks Erlenmeyer flasks beakers round-bottom flask with septum inlet three-neck vertical round-bottom flask test tube funnel powder funnel Büchner funnel rubber stoppers glass stoppers filtering flasks volumetric flasks with stoppers separatory funnels dropping funnels vacuum-distilling adapter Claisen adapters straight-connecting adapters offset adapter three-way adapter reducing adapters thermometers burette pipettes Graham condenser West condenser Reflux condenser Liebig condenser Bunsen burner Meker-Bunsen burner rotatory evaporator trap trap pestle mortar mixer crucibles burette holder (clamp) support stand clamp round-bottom flask tripod stand gauze with ceramic insert distillation apparatus cooling water receiving flask separation apparatus alteration adapter beaker blanket bottle bottom burner calcine calcining circle ceramic clamp (holder) combustion spoon condenser conical container cork crucible tongs desiccator dish distillation dropping evolve extinguisher flask fluid fume chamber gauze glass rod glassware graduation heating ignite insert layer lid liquid melt neck opening pinchcock pour powder reagent round secure separation separatory septum inlet solvent spirit burner stopcock straight sulphur throw out tip tongs transferring tube vessel volumetric volumetric flask volumetric cylinder wash bottle watch glass Lesson 2 aerosol aqueous solution atomic mass unit atomic relative mass boiling chemical substance coarse composition compound condensation consist of crystallisation density desublimation detergent dilute dissolved distillation distinct electric field element emulsion evaporate evaporation evenly extraction filtration float foam fog freezing gas gaseous state gravitational field heterogenous homogenous immiscible insoluble involve link liquid liquid state magnetic field mass percent matter melting miscible mix mixture mol molarity mole fraction molecular relative mass particle pure substance saturated solution sediment separation shake smoke solid solid state solubility solubility curve soluble solute solution solvent stir stock solution sublimation substance suspension system take on to form vapour volatile Lesson 3 boiling point centrifugate centrifugation centrifuge centrifuging constituent crystallization crystals decantation dissociate distil distillate distillation distilled water embedded evaporate evaporation filter cake filter paper filtering filtrate filtration force fractional distillation homogenate chromatogram chromatography identify impure impurity microscope slide porous precipitate reagent residue scales, balance sedimentation separate separating funnel settle sublimation vapour (brit.), vapor (am.) water bath to weigh Chemical Elements Actinium Aluminium Aluminum Americium Antimony Argon Arsenic Astatine Barium Berkelium Beryllium Bismuth Bohrium Boron Bromine Cadmium Caesium Calcium Californium Carbon Cerium Cesium Chlorine Chromium Cobalt Copernicium Copper Curium Darmstadtium Dubnium Dysprosium Einsteinium Erbium Europium Fermium Flerovium Fluorine Francium Gadolinium Gallium Germanium Gold Hafnium Hassium Helium Holmium Hydrogen Indium Iodine Iridium Iron Krypton Lanthanum Lawrencium Lead Lithium Livermorium Lutetium Magnesium Manganese Meitnerium Mendelevium Mercury Molybdenum Neodymium Neon Neptunium Nickel Niobium Nitrogen Nobelium Osmium Oxygen Palladium Phosphorus Platinum Plutonium Polonium Potassium Praseodymium Promethium Protactinium Radium Radon Rhenium Rhodium Roentgenium Rubidium Ruthenium Rutherfordium Samarium Scandium Seaborgium Selenium Silicon Silver Sodium Strontium Sulphur Tantalum Technetium Tellurium Terbium Thallium Thorium Thulium Tin Titanium Tungsten Ununoctium Ununpentium Ununseptium Ununtrium Uranium Vanadium Xenon Ytterbium Yttrium Zinc Zirconium Nomenclature of Inorganic Compounds A compound can be identified either by its formula (e. g. NaCl) or its name (sodium chloride). In this section, you will learn the rules used to name ionic and simple molecular compounds. To start with, it will be helpful to show how individual ions within ionic compounds are named. Ions Monatomic cations take the name of the metal from which they are derived. Examples include Na^+ sodium K^+ potassium There is one complication: Certain metals, notably those in the transition series, form more than one type of cation. An example is iron, which forms both Fe^2+ and Fe^3+. To distinguish between these cations, the charge must be indicated in the name. This is done by putting the charge as a Roman numeral in parentheses after the name of the metal: Fe^2+ iron(II) Fe^3+ iron(III) An older system used the suffixes -ic for the ion fo higher charge and -ous for the ion of the lower charge. These were added to the stem of the Latin name of the metal, so that the Fe^3+ ion was referred to as ferric and the Fe^2+ as ferrous. Monatomic anions are named by adding the suffix -ide to the stem of the name of the nonmetal from which they are derived. N^3– nitride O^2– oxide S^2– sulphide Se^2– selenide Te^2– telluride H^– hydride F^– fluoride Cl^– chloride Br^– bromide I^– iodide Polyatomic ions are given special names: NH[4]^+ ammonium OH^– hydroxide NO[3]^– nitrate ClO[3]^– chlorate ClO[4]^– perchlorate CN^– cyanide CH[3]COO^– acetate MnO[4]^– permanganate CO[3]^2– carbonate HCO[3]^– hydrogen carbonate PO[4]^3– phosphate HPO[4]^2– hydrogen phosphate H[2]PO[4]^– dihydrogen phosphate SO[4]^2– sulphate CrO[4]^2– chromate Cr[2]O[7]^2– dichromate Certain nonmetals in Groups 15-17 of the periodic table form more than one polyatomic ion containing oxygen (oxoanions). The names of several such oxoanions are shown in below. From the entries in the table, you should to be able to deduce the following rules: 1. When a nonmetal forms two oxoanions, the suffix -ate is used for the anion with the larger number of oxygen atoms. The suffix -ite is used for the anion containing fewer oxygen atoms. 2. When a nonmetal forms more than two oxoanions, the prefixes per- (largest number of oxygen atoms) and hypo- (fewest oxygen atoms) are used as well. Oxoanions of nitrogen, sulphur and chlorine Nitrogen NO[3]^– nitrate NO[2]^– nitrite Sulphur SO[4]^2– sulphate SO[3]^2– sulphite Chlorine ClO[4]^– perchlorate ClO[3]^– chlorate ClO[2]^– chlorite ClO^– hypochlorite Ionic compounds The name of an ionic compound consists of two words. The first word names the cation and the second names the anion. This is, of course, the same order in which the ions appear in the formula. Example: CaS calcium sulphide Al(NO[3])[3] aluminium nitrate FeCl[2] iron(II) chloride Binary molecular compounds When a metal combines with a nonmetal, the product is ordinarily an ionic compound. As you have just seen, the formulas and names of these compounds can be deduced in a straightforward way. Shen two nonmetals combine with each other, the product is most often a binary molecular compound. There is no simple way to deduce the formulas of such compounds. There is, however, a systematic way of naming molecular compounds that differs considerably from that used with ionic compounds. The systematic name of a binary molecular compound, which contains two different nonmetals, consists of two words: 1. The first word gives the name of the element that appears first in the formula; a Greek prefix (see below) is used to show the number of atoms of that element in the formula. 2. The second word consists of - the appropriate Greek prefix designating the number of atoms of the second element - the stem of the name of the second element - the suffix -ide To ilustrate these rules, consider the names of the several oxides of nitrogen: Example: N[2]O[5] dinitrogen pentaoxide NO[2] nitrogen dioxide NO nitrogen oxide N[2]O[4] dinitrogen tetraoxide N[2]O[3] dinitrogen trioxide N[2]O dinitrogen oxide Greek prefixes used in nomenclature Number Prefix 2 di 3 tri 4 tetra 5 penta 6 hexa 7 hepta 8 octo 9 nona 10 deca Example: SO[2] sulphur dioxide SO[3] sulphur trioxide PCl[3] phosphorus trichloride Cl[2]O[7] dichlorine heptaoxide Many of the best-known binary compounds of the nonmetals have acquired common names. These are widely and, in some cases, exclusively used. Example: H[2]O water H[2]O[2] hydrogen peroxide NH[3] ammonia N[2]H[4] hydrazine C[2]H[2] acetylene PH[3] phosphine AsH[3] arsine NO nitric oxide N[2]O nitrous oxide CH[4] methane Acids A few binary molecular compounds containing H atoms ionize in water to form H^+ ions. These are called acids. One such compound is hydrogen chloride, HCl; in water solution it exists as aqueous H^+ and Cl^– ions. The water solution of hydrogen chloride is given a special name; it is referred to as hydrochloric acid. A similar situation applies with HBr and HI: Pure substance Water solution HCl (g) hydrogen chloride H^+(aq), Cl^–(aq) hydrochloric acid HBr (g) hydrogen bromide H^+(aq), Br^–(aq) hydrobromic acid HI (g) hydrogen iodide H^+(aq), I^–(aq) hydroiodic acid Most acids contain oxygen in addition to hydrogen atoms. Such species are referred to as oxoacids. Two oxoacids that you are likely to encounter in the general chemistry laboratory are: HNO[3] nitric acid H[2]SO[4] sulphuric acid The names of oxoacids are simply related to those of the corresponding oxoanions. The -ate suffix of the anion is replaced by -ic in the acid. Similarly, the suffix -ite is replaced by the suffix -ous. The prefixes per- and hypo- found in the name of the anion are retained in the name of the acid. Example: ClO[4]^– perchlorate ion HClO[4] perchloric acid ClO[3]^– chlorate ion HClO[3] chloric acid ClO[2]^– chlorite ion HClO[2] chlorous acid ClO^– hypochlorite ion HClO hypochlorous acid Nomenclature of Organic Compounds Nomenclature of Alkanes Straight-Chain Alkanes: methane, ethane, propane, butane, pentane, hexane, heptane, octane Alkyl Groups:methyl, ethyl, propyl, isopropyl, butyl With alkanes containing a branched chain, the name is more complex. A branched-chain alkane such as 2-methylpropane can be considered to be derived from a straight-chain alkane by replacing one or more hydrogen atoms by alkyl groups. The name consists of two parts: · a suffix that identifies the parent straight-chain alkane. To find the suffix count the number of carbon atoms in the longest continuous chain. For a three-carbon chain, the suffix is propane; for a four-carbon chain it is butane, and so on. · a prefix that identifies the branching alkyl group and indicates by a number the carbon atom where branching occurs. In 2-methylpropane, referred to above, the methyl group is located at the second carbon from the end of the chain: pentane, 2-methylbutane, 2,2-dimethylpropane If the same alkyl group is at two branches, the prefix di- is used (2,2-dimethylpropane). If there were three methyl branches, we would write trimethyl, and so on. The number in the name is made as small as possible. Thus, we refer to 2-methylbutane, numbering the chain from the left, rather than from the right. Nomenclature of Alkenes The systematic names of alkenes are derived from those of the corresponding alkanes with the same number of carbon atoms per molecule. There are two modifications. · the ending –ane is replaced by –ene: ethane, ethene · where necessary, a number is used to designate the double-bonded carbon; the number is made as small as possible: but-1-ene, but-2-ene, 2-methylbut-1-ene, 2-methylbut-2-ene, cis-but-2-ene, trans-but-2-ene Nomenclature of Alkynes The IUPAC names of alkynes are derived from those of the corresponding alkenes by replacing the suffix –ene with –yne: ethyne, propyne, but-1-yne, but-2-yne Derivatives of Benzene Monosubstituted benzenes are ordinarily named as derivatives of benzene: Chlorbenzene, nitrobenzene, aminobenzene, hydroxybenzene, methylbenzene The last three compounds listed are always referred to by their common names (aniline, phenol, toluene). Functional Groups Many organic molecules can be considered to be derived from hydrocarbons by substituting a functional group for a hydrogen atom. The functional group can be a nonmetal atom or small group of atoms that is bonded to carbon. Classes of organic molecules containing common functional groups: halides, alcohols, ethers, aldehydes, ketones, carboxylic acids, esters, amines, amides. Examples of compounds: choloroethane, ethanol, dimethyl ether, ethanal, propanone, ethanoic acid, methyl methanoate, aminomethane, ethanamide Carboxylic Acids The [ ]systematic names of these compounds are obtained by adding the suffix –oic to the stem of the name of the corresponding alkanes. In practice, these names are seldom used for the first two members of the series, which are commonly referred to as formic acid and acetic acid. Examples: methanoic acid = formic acid, ethanoic acid = acetic acid, citric acid, malic acid, oxalic acid Test 1 malic acid, but-2-ene, pentane, pent-1, 3-diene, butanoic acid, aminobenzene, propanone, 3-methylbutan-2-ol. Test 2 ethanoic acid, ethanal, nitrobenzenepropyne, trans-but-2-ene, pent-2,3-diene, hexane, 2-methylbut-2-ene, hept-1,3-diyne, phenol, aminomethane, but-2-ene-1-ol General Chemistry absorbance absorption of radiation electron affinity actinides a-helix aluminosilicate volumetric analysis gravimetric analysis aniline antiparticle activation barrier baryon soft base hard base benzene protein biochemistry stationary point borane boson intermediate boson butadiene reaction path a particle b particle particle of force field atomic number Avogadro´s number quantum number principal quantum number magnetic quantum number orbital angular momentum quantum number mass number proton number degenaracy of state bond lenght wavelength derivative deuterium diffusion dissociation particle-wave duality nonadiabatic effect electrolyte strong electrolyte weak electrolyte elektrolysis electron electronegativity emission of radiation energy activation energy total energy discrimination energy dissociation energy photon energy Gibbs (free) energy standard Gibbs energy Helmholtz energy kinetic energy zero-point energy orbital energy potential energy potential energy curve vibrational energy internal energy enthalpy enthalpy of reaction standard enthalpy of formation entropy enzyme ethylene fermion fluidity fluorescence phosphorescence photon collision frequency frequency of radiation function state function wave function symmetry properties of wave function electron wave function nuclear fusion gene geometry of molecule graphite graviton group point group hadron Hamiltonian helium atomic mass molecular mass electron density, distribution probability density (linear) momentum hybridization potential energy hypersurface analytical chemistry inorganic chemistry physical chemistry organic chemistry chirality chromatography chromosome angular momentum genetic information graphical integration numerical integration integral indefinite integral constant of motion overlap integral definite integral Coulomb interaction electromagnetic interaction gravitational interaction strong interaction weak interaction hydrogen molecular ion insulator isomer atomic nucleus carcinogenic activity of hydrocarbons heat capacity catalysis acid catalysis hydronium cation cluster molar absorption coefficient expansion coefficient activated complex transition complex charge-transfer complex electron configuration dissociation constant Planck constant (universal) gas constant equilibrium constant rate constant energy continuum reaction coordinate ionic crystal liquid crystal covalent crystal molecular crystal potential-energy curve quantization quantization of energy quark deoxyribonucleic acid soft acid nucleic acid hard acid lanthanides laser amorphous solids crystalline solids lepton ligand classical mechanics statistical mechanics donor-acceptor mechanism reaction mechanism metallocene metalloid reaction intermediate meson muon amount of substance antibonding MO bonding MO cyclic molecule molecularity of reaction angular momentum orbital angular momentum magnetic moment transition moment spin multiplicity naphtalene nonmetal indistinguishability of particles neutralization neutrino neutron nucleoside nucleotide nuclide molar volume inversion (operation) symmetry operation operator Hamilton operator (Hamiltonian) Laplace operator (Laplacian) atomic orbital hybrid orbital molecular orbital unoccupied (virtual) orbital occupied orbital valence orbital p orbital d orbital s orbital symmetry axis electron pair absorption band energy band valence band conduction band period (row) of elements permittivity (dielectric constant) pH, measure of acidity ideal gas real gas synthesis gas noble gas boundary condition initial condition computational experiment polarography half-life for radioactive decay semiconductor bathochromic shift hypsochromic shift ionization potential positron Hund rule rule of maximum multiplicity selection rule Heisenberg uncertainty principle building-up (Aufbau) principle principle of equipartition of energy Pauli exclusion principle absorption process adiabatic process emission process irreversible process reversible process product of reaction ion product constant of water proton transition element symmetry element spectral transition pyridine radical induced radioactivity spontaneous radioactivity bimolecular reaction endothermic reaction exothermic reaction photochemical reaction monomolecular (unimolecular) reaction first-order reaction reduction-oxidation reaction kinetically controlled reaction thermodynamically controlled reaction trimolecular (termolecular) reaction reactant reduction Coulomb repulsion rotation Clausius-Clapeyron equation differential equation equation of state for the ideal gas van der Waals equation acid-base equilibrium catalytic decomposition radioactive decay reaction rate decay rate velocity of light reaction order orbital scheme state scheme intermolecular forces physical state group of elements conjugated compound nonstoichiometric compound electron shell closed shell solvolysis spectrometer mass spectrometry infrared spectroscopy microwave spectroscopy electronic spectrum rotational spectrum vibrational- rotational spectrum spin elastic collision inelastic collision reactive collision electronic state liquid state quantum state state of a substance solid (state) gaseous state resonance phenomenon rotational state equilibrium singlet state stationary state standard state excited state ground state stoichiometry molecular structure centre of symmetry degree of degeneracy vibrational degree of freedom superconductivity symmetry nuclear fission Bohr theory quantum theory collision theory heat heat of sublimation heat of vaporization absolute (Kelvin) temperature thermodynamics chemical thermodynamics thiophene system trajectory tritium mass defect dihedral angle bond angle aliphatic hydrocarbon alternant hydrocarbon cyclic hydrocarbon saturated hydrocarbon nonalternant hydrocarbon unsaturated hydrocarbon double bond chemical bond peptide bond triple bond hydrogen bond vibration vibration of a bond viscosity extensive property intensive property conductor electron shell Einstein relation weakon Hess law Lambert-Beer law Maxwell-Boltzmann energy-distribution law law of conservation of energy electromagnetic radiation zeolite reflection