CHEMISTRY GLOSSARY

artificial honey    →   umjetni med

Artificial honey is the old synonym for invert sugar syrup.

honey    →   med

Honey is a sweet, amber colored, viscous fluid produced by honeybees from the nectar of flowers. It is composed primarily of fructose (about 40 %), glucose (about 35 %), and water (up to 20 %). In addition, honey contains sucrose, maltose, trisaccharides, and small amounts of minerals, vitamins, and enzymes.

bohrium    →   bohrij

Bohrium was discovered by Peter Armbruster, Gottfried Münzenber and their co-workers at the Heavy Ion Research Laboratory (Gesellschaft für Schwerionenforschung, GSI) in Darmstadt, Germany in 1981. Named in honour of Niels Bohr, the Danish physicist. It is synthetic radioactive metal. Bohrium was produced by bombarding bismuth-204 with chromium-54.

curium    →   kurij

Curium was discovered by Glenn T. Seaborg, Ralph A. James and Albert Ghiorso (USA) in 1944. Named in honour of Pierre and Marie Curie. It is silvery, malleable, synthetic radioactive metal. So radioactive it glows in the dark. Curium was made by bombarding plutonium with helium ions.

darmstadtium    →   darmstadtij

Darmstadtium was discovered by S. Hofmann et al. collaboration at the Heavy Ion Research Laboratory (Gesellschaft für Schwerionenforschung, GSI) in Darmstadt, Germany in November 1994. The title honours the Laboratory for Heavy Ion Research (called GSI) in Darmstadt, Germany, where the substance was first made. It is synthetic radioactive metal. The fusion-evaporation reaction using a ⁶²Ni beam on an isotopically enriched ²⁰⁸Pb target produced four chains of alpha-emitting nuclides following the presumed formation of ²⁶⁹110 + ¹n.

einsteinium    →   einsteinij

Einsteinium was discovered by Albert Ghiorso (USA) in 1952. Named in honour of Albert Einstein (1879-1955). It is synthetic radioactive metal. Einsteinium was made by bombarding uranium with neutrons.

fermium    →   fermij

Fermium was discovered by Albert Ghiorso (USA) in 1953. Named in honour of Enrico Fermi. It is synthetic radioactive metal. Fermium was produced by bombarding lighter transuranium elements with still lighter particles or by neutron capture.

fructose    →   fruktoza

Fructose (fruit sugar) is a ketohexose (a six-carbon ketonic sugar), which occurs in sweet fruits and honey. Glucose and fructose have the same molecular formula, C₆H₁₂O₆, but have different structures. Pure, dry fructose is a very sweet, white, odorless, crystalline solid. Fructose is one of the sweetest of all sugars and is combined with glucose to make sucrose, or common table sugar. An older common name for fructose is levulose, after its levorotatory property of rotating plane polarized light to the left (in contrast to glucose which is dextrorotatory). The polysaccharide inulin is a polymer of fructose.

meitnerium    →   meitnerij

Meitnerium was discovered by Peter Armbruster, Gottfried Münzenber and their co-workers at the Heavy Ion Research Laboratory (Gesellschaft für Schwerionenforschung, GSI) in Darmstadt, Germany in 1982. Named in honour of Lise Meitner (1878-1968), the Austrian physicist. It is synthetic radioactive metal. Meitnerium was produced bybombarding bismuth-209 with iron-58.

glucose    →   glukoza

Glucose (grape sugar, blood sugar), C₆H₁₂O₆, is an aldohexose (a monosaccharide sugar having six carbon atoms and an aldehyde group). An older common name for glucose is dextrose, after its dextrorotatory property of rotating plane polarized light to the right. Glucose in free (in sweet fruits and honey) or combined form (sucrose, starch, cellulose, glycogen) is is probably the most abundant organic compound in nature. During the photosynthesis process, plants use energy from the sun, water from the soil and carbon dioxide gas from the air to make glucose. In cellular respiration, glucose is ultimately broken down to yield carbon dioxide and water, and the energy from this process is stored as ATP molecules (36 molecules of ATP across all processes).

Naturally occurring glucose is D isomers (OH group on the stereogenic carbon farthest from the aldehyde group, C-5, is to the right in the Fischer projection). Although often displayed as an open chain structure, glucose and most common sugars exist as ring structures. In the α form, the hydroxyl group attached to C-1 and the CH₂OH attached to C-5 are located on opposite sides of the ring. β-glucose has these two groups on the same side of the ring. The full names for these two anomers of glucose are α-D-glucopyranose and β-D-glucopyranose.