CHEMISTRY GLOSSARY

cyclic compound    →   ciklički spoj

Cyclic describing a compound that has a ring of atoms in its molecules. In homocyclic compounds all the atoms in the ring are of the same type, e.g. benzene (C₆H₆) and cyclohexane (C₆H₁₂). These two examples are also examples of carbocyclic compounds; i.e. the rings are made of carbon atoms. If different atoms occur in the ring, as in pyridine (C₅H₅N), the compound is said to be heterocyclic.

cyclic voltammetry    →   ciklička voltametrija

Cyclic voltammetry (CV) is an electrochemical measuring technique used for the determination of the kinetics and mechanism of electrode reactions. The potential of the working electrode is controlled (typically with a potentiostat) and the current flowing through the electrode is measured. It is a linear-weep voltammetry with the scan continued in the reverse direction at the end of the first scan. This cycle can be repeated a number of times, and is used for corrosion studies.

cyclization    →   ciklizacija

Cyclization is the formation of a cyclic compound from an open-chain compound.

aliphatic compound    →   alifatski spoj

Aliphatic compounds are acyclic or cyclic, saturated or unsaturated carbon compounds, excluding aromatic compounds.

anomer    →   anomer

Anomers are diastereoisomers of cyclic forms of sugars or similar molecules differing in the configuration at the anomeric carbon (C-1 atom of an aldose or the C-2 atom of a 2-ketose). The cyclic forms of carbohydrates can exist in two forms, α- and β- based on the position of the substituent at the anomeric center. Anomer are designated α if the configuration at the anomeric carbon is the same as that at the reference asymmetric carbon in a Fischer projection. If the configuration differs the anomer is designated β. For example, α-D-glucopyranose and β-D-glucopyranose, the two cyclic forms of glucose, are anomers.

aromatic compounds    →   aromatski ugljikovodici

Aromatic compounds are a major group of unsaturated cyclic hydrocarbons containing one or more rings, typified by benzene, which has a 6-carbon ring containing three double bonds. All the bonds in benzene (C₆H₆) are the same length intermediate between double and single C-C bonds. The properties arise because the electrons in the p-orbitals are delocalised over the ring, giving extra stabilization energy of 150 kJ/mol over the energy of Kekulé structure. Aromatic compounds are unsaturated compounds, yet they do not easily partake in addition reactions.

Historical use of the term implies a ring containing only carbon (e.g., benzene, naphthalene), but it is often generalized to include heterocyclic structures such as pyridine and thiophene.

cycloalkanes    →   cikloalkani

Cycloalkanes are cyclic saturated hydrocarbons containing a ring of carbon atoms joined by single bonds. They have the general formula C_nH_2n, for example cyclohexane, C₆H₁₂. In general, they behave like the alkanes but are rather less reactive.

heterocyclic compounds    →   heterociklički spojevi

Heterocyclic compounds are cyclic compounds having as ring members atoms of at least two different elements, e.g., quinoline, 1,2-thiazole.

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.

hemiacetal    →   poluacetal

Hemiacetals are organic compounds having the general formula R₂C(OH)OR’ (R’ ≠ H), derived from aldehydes or ketones by formal addition of an alcohol to the carbonyl group. Hemiacetals are generally unstable compounds. In some cases however, stable cyclic hemiacetals can be readily formed, especially when 5- and 6-membered rings are possible. In this case an intramolecular OH group reacts with the carbonyl group. Glucose and many other aldoses exist as cyclic hemiacetals whereas fructose and similar ketoses exist as cyclic hemiketals. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H).