CHEMISTRY GLOSSARY

non-polar solvent    →   nepolarno otapalo

Non-polar solvent is a liquid with non-polar molecules. It dissolves covalent compounds, non-water solvent.

olefin    →   olefin

Olefins are acyclic and cyclic hydrocarbons having one or more carbon-carbon double bonds, apart from the formal ones in aromatic compounds. The class olefins subsume alkenes and cycloalkenes and the corresponding polyenes.

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.

hafnium    →   hafnij

Hafnium was discovered by Dirk Coster (Denmark) and Georg Karl von Hevesy (Hungary) in 1923. The origin of the name comes from the Latin name Hafnia meaning Copenhagen. It is silvery, ductile metal. Exposed surfaces form oxide film. Resists alkalis and acids (except HF). Toxic. Metal ignites and burns readily. Hafnium is obtained from mineral zircon or baddeleyite. Used in reactor control rods because of its ability to absorb neutrons.

ore    →   ruda

Ores are natural mineral aggregates (compounds in which metals are found in nature) from which get one or more metals can be obtained rentably. Except for minerals, ore also contains some other ingredients which do not have any technical value and are usually called waste.

organic chemistry    →   organska kemija

Organic chemistry is a science about all compounds which consist of carbon atoms, except carbonates and oxides of carbon.

organometallic compound    →   organometalni spoj

Organometallic compounds are compounds in which there is a covalent connection between atoms of carbons and atoms of metal (C-Me).

oxidation    →   oksidacija

The term oxidation originally meant a reaction in which oxygen combines chemically with another substance. More generally, oxidation is a part of a chemical reaction in which a reactant loses electrons (increases oxidation number). Simultaneous reduction of a different reactant must occur (redox reaction).

oxime    →   oksim

Oximes are organic compounds of structure R₂C=NOH derived from condensation of aldehydes or ketones with hydroxylamine. Oximes from aldehydes may be called aldoximes; those from ketones may be called ketoximes.

glycoside    →   glikozid

Glycoside is one of a group of organic compounds in which a sugar group is bonded through its anomeric carbon to another group via a glycosidic bond. The sugar group is known as the glycon and the non-sugar group as the aglycon. According to the IUPAC definition, all disaccharides and polysaccharides are glycosides where the aglycone is another sugar.

In the free hemiacetal form, sugars will spontaneously equilibrate between the α and β anomers. However, once the glycosidic bond is formed, the anomeric configuration of the ring is locked as either α or β. Therefore, the alpha and beta glycosides are chemically distinct. They will have different chemical, physical, and biological properties. Many glycosides occur abundantly in plants, especially as flower and fruit pigments.

The term glycoside was later extended to cover not only compounds in which the anomeric hydroxy group is replaced by a group -OR, but also those in which the replacing group is -SR (thioglycosides), -SeR (selenoglycosides), -NR1R2 (N-glycosides), or even -CR1R2R3 (C-glycosides). Thioglycoside and selenoglycoside are legitimate generic terms; however the use of N-glycoside, although widespread in biochemical literature, is improper and not recommended here (glycosylamine is a perfectly acceptable term). C-Glycoside is even less acceptable. All other glycosides are hydrolysable; the C-C bond of C-glycosides is usually not. The use and propagation of names based on C-glycoside terminology is therefore strongly discouraged.