CHEMISTRY GLOSSARY

promethium    →   prometij

Promethium was discovered by J. A. Marinsky, Lawrence Glendenin and Charles D. Coryell (USA) in 1945. Named after Prometheus in Greek mythology, who stole fire from the gods. It is rare earth metal of synthetic origin on the earth, naturally made in stars. Poison. Radiotoxic. Radioactive. Promethium does not occur naturally. Found among fission products of uranium, thorium and plutonium. It has been used as a source of radioactivity for thickness-measuring gages.

ununbium    →   ununbij

Ununbium was discovered by S. Hofmann et al. collaboration at the Heavy Ion Research Laboratory (Gesellschaft für Schwerionenforschung, GSI) in Darmstadt, Germany in February 1996. The new element has not yet been officially named, but it is known as ununbium, according to the system designated by the IUPAC for naming new elements. It is synthetic radioactive metal. Using the electromagnetic velocity filter SHIP, fusion-like residues of the reaction of ⁷⁰Zn with enriched ²⁰⁸Pb targets were measured. Two chains of localized alpha-emitters were identified as originating with ²⁷⁷112 + ¹n.

acetal    →   acetal

Acetals are organic compounds having the structure R₂C(OR’)₂ (R’ ≠ H). They are organic compounds formed by addition of alcohol molecules to aldehyde or ketone molecules. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H ). Mixed acetals have different R’ groups. The formation of acetals is reversible; acetals can be hydrolysed back to aldehydes (ketone) in acidic solutions.

Acetal, 1,1-diethoxyethane (CH₃CH(OC₂H₅)₂), is an organic compound, pleasant smelling, formed by addition of ethyl alcohol to ethanal (acetaldehyde). It is used as a solvent and in synthetic organic chemistry.

Acheson process    →   Achesonov proces

Acheson process is an industrial process to synthesize graphite and silicon carbide (carborundum), named after its inventor the American chemist Edward Goodrich Acheson (1856-1931). In this process, a solid-state reaction between pure silica sand (SiO₂) and petroleum coke (C) at very high temperature (more than 2500 °C) leads to the formation of silicon carbide under the general reaction:

While studying the effects of high temperature on carborundum, Acheson had found that silicon vaporizes at about 4150 °C, leaving behind graphitic carbon.

actinium    →   aktinij

Actinium was discovered by André Debierne (France) in 1899. The origin of the name comes from the Greek word aktinos meaning ray. It is heavy, silvery-white, very radioactive metal. Reacts with water. Glows in the dark. Actinium is extremely rare, found in all uranium ores. Usually obtained by treating radium with neutrons in a reactor.

alkanes    →   alkani

Alkanes (paraffins) are acyclic branched or unbranched hydrocarbons having the general formula C_nH_2n+2, and therefore consisting entirely of hydrogen atoms and saturated carbon atoms. In the systematic chemical nomenclature alkane names end in the suffix -ane. They form a homologous series (the alkane series) methane (CH₄), ethane (C₂H₆), propane (C₃H₈), butane (C₄H₁₀), etc. The lower members of the series are gases; the high-molecular mass alkanes are waxy solid. Generaly the alkanes are fairly unreactive. They form haloalkanes with halogens when irradiated with ultraviolet radiation. Alkanes are present in natural gas and petroleum.

americium    →   americij

Americium was discovered by Glenn T. Seaborg, Ralph A. James, Stanley G. Thompson and Albert Ghiorso (USA) in 1944. Named for the American continent. It is silvery-white, artificially produced radioactive metal. Americium was produced by bombarding plutonium with neutrons. Americium-241 is currently used in smoke detectors.

becquerel    →   bekerel

Becquerel (Bq) is the SI derived unit, with a special name, for radioactivity, equal to s^-1. It describes a radioactivity of an amount of radionuclide decaying at the rate, on average, of one spontaneous nuclear transition per second. The unit was named after the French scientist Antoine Henri Becquerel (1852-1908) (disintegrations per unit time), equal to s^-1.

alkenes    →   alkeni

Alkenes are acyclic branched or unbranched hydrocarbons having one or more double carbon-carbon bonds in their molecules. In the systematic chemical nomenclature, alkene names end in the suffix -ene. The general formula is C_nH_(2n+2)-2x were x is the number of double bonds. Alkenes that have only one double bond form a homologous series: ethene (ethylene), CH₂=CH₂, propene, CH₃CH₂=CH₂, etc. Alkenes typically undergo addition reactions to the double bond.

alkynes    →   alkini

Alkynes (acetylenes) are acyclic branched or unbranched hydrocarbons having one or more triple carbon-carbon bond. In the systematic chemical nomenclature alkyne names end in the suffix -yne. The general formula is C_nH_(2n+2)-4x were x is the number of triple bonds. Alkynes that have only one triple bond form a homologous series: ethyne (acetylene), CH≡CH, propyne, CH₃CH≡CH, etc. Like alkenes, alkynes undergo addition reaction.