CHEMISTRY GLOSSARY

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.

haematite    →   hematit

Haematite is a mineral of iron(III) oxide Fe₂O₃. It is the most important ore of iron and usually occurs in two main forms: as a massive red kidney-shaped ore and as grey to black metallic crystals known as specular iron ore. Haematite is the major red colouring agent in rocks; the largest deposits are of sedimentary origin. In industry haematite is also used as a polishing agent (jeweller’s rouge) and in paints.

quantum chemistry    →   kvantna kemija

Quantum chemistry is a theoretical branch of chemistry that concerns the application of quantum mechanics to chemical problems.

racemisation    →   racemizacija

Racemisation is a conversion, by heat or by chemical reaction, of an optically active compound into an optically inactive form which half of the optically active substance becomes its miror image (enantiomer).

reactant    →   reaktant

Reactants are initial materials in a chemical reaction.

reaction mechanism    →   reakcijski mehanizam

Reaction mechanism is a list of all elementary reactions that occur in the course of an overall chemical reaction.

reactivity    →   reaktivnost

Reactivity is the tendency of a compound to chemically react with other substances or itself, resulting in the release of energy.

reagent    →   reagens

Reagents are any substance used in a chemical reaction to detect, measure, examine, or produce other substances.

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.

halocarbon    →   halogenirani ugljikovodik

Halocarbon is a compound containing no elements other than carbon, one or more halogens, and sometimes hydrogen. The simplest are compounds such as tetrachloromethane (CCl₄), tetrabromomethane (CBr₄), etc. The lower members of the various homologous series are used as refrigerants, propellant gases, fireextinguishing agents, and blowing agents for urethane foams. When polymerized, they yield plastics characterized by extreme chemical resistance, high electrical resistivity, and good heat resistance.