CHEMISTRY GLOSSARY

ether    →   eter

Ethers are organic compounds with a formula R-O-R, where R is not equal to H. They may be derived from alcohols by elimination of water, but the major method is catalytic hydration of olefins. They are volatile highly flammable compounds; when containing peroxides they can detonate on heating. The term ether is often used synonymously with diethyl ether.

acetylene    →   acetilen

Acetylene (ethyne) is a colourless unstable gas, C₂H₂, with a characteristic sweet odour. It is lighter than air, easily soluble in acetone (propanone) and it is explosive under high pressure.

addition reactions    →   reakcije adicije

Addition reactions are normally occur with unsaturated compounds and involve the addition of one molecule (called the reactant) across the unsaturated bond (i.e. the double bond or the triple bond) of another molecule (called the substrate) to give a single product, formed by the combination of both reacting molecules.

For example, bromine adds across the double bond of ethene in an addition reaction to form dibromoethane.

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.

benzene    →   benzen

Benzene is a colourless liquid hydrocarbon, C₆H₆, b.p. 80 °C. It is now made from petroleum by catalytic reforming (formerly obtained from coal tar). Benzene is the archetypal aromatic compound. It has an unsaturated molecule, yet will not readily undergo addition reactions. On the other hand, it does undergo substitution reactions in which hydrogen atoms are replaced by other atoms or groups.

In 1865, Friedrich August Kekulé purposed the benzene molecule structure as a hexagonal ring which consists of six carbon atoms with alternate carbon-carbon single and carbon-carbon double bond. But such a structure should be highly reactive, and so didn't account for the unreactive nature of benzene. We now know that the best representation for the structure of benzene is indeed, hexagonal, with each C-C bond distance being identical and intermediate between those for a single and double bond. The π-orbitals from each neighbouring carbon atom overlap to form a delocalised molecular orbital which extends around the ring, giving added stability and with it, decreased reactivity. That is the reason the structural formula of benzene represents as a hexagon with a circle in the center which represents the delocalized electrons.

perfume    →   parfem

Perfumes are mixtures or alcohol solutions of natural or synthetic volatile substances of a pleasant aroma, usually containing plant ethereal oils or relative esters, ethers, aldehydes and ketones.

selenide    →   selenid

Selenides are compounds having the structure R-Se-R (R not equal to H). They are thus selenium analogues of ethers. Also used for metal salts of H₂Se.

epoxy resin    →   epoksi smola

Epoxy resins are thermosetting resins produced by copolymerising epoxide compounds with phenols (e.g. epichlorohydrin and bisphenol A). They contain ether linkages (-O-) and form a tight, cross-linked polymer network. Toughness, good adhesion, corrosive-chemical resistance, and good dielectric properties characterise epoxy resins. Most epoxy resins are two-part types which harden when blended.

styrene    →   stiren

Styrene is an unsaturated hydrocarbon (C₆H₅OC₂H₃O) colourless, toxic liquid with a strong aromatic aroma. It is soluble in alcohol, ether, acetone, and carbon disulfide, but dissolves only slightly in water. It is used to make plastics such as polystyrene, ABS, styrene-butadiene rubber styrene-butadiene latex and unsaturated polyesters.