CHEMISTRY GLOSSARY

alkali metal    →   alkalijski metal

Alkali metal is a term that refers to six elements: lithium (Li), sodium (Na), potassium (K), rubidium (Rb), caesium (Cs), and francium (Fr). These elements make up group 1 of the periodic table of elements. They all form singly charged positive ions, and are extremely reactive. They react violently with water, forming hydroxides and releasing hydrogen gas and heat. Caesium and francium are the most reactive and lithium is the least.

alkaline earth metal    →   zemnoalkalijski metal

Alkali earth metal is a term that refers to six elements: beryllium (Be), magnesium (Mg), calcium (Ca), strontium (Sr), barium (Ba), and radium (Ra). These elements make up group 2 of the periodic table of elements. They all exhibit a single oxidation state, +2. They are all light and very reactive. Barium and radium are the most reactive and beryllium is the least.

To denote slightly soluble metal oxides chemists formerly used the term "earth". The oxides of barium, strontium, and calcium resemble alumina (Al₂O₃), a typical "earth", but form alkaline mixtures with water. For this reason barium, strontium, and calcium were called alkaline earth metals. This name has now been extended to include all of the elements of group 2.

alkanes    →   alkani

Alkanes (paraffins) are acyclic branched or unbranched hydrocarbons having the general formula C_nH_2n+2, and therefore consisting entirely of hydrogen atoms and saturated carbon atoms. In the systematic chemical nomenclature alkane names end in the suffix -ane. They form a homologous series (the alkane series) methane (CH₄), ethane (C₂H₆), propane (C₃H₈), butane (C₄H₁₀), etc. The lower members of the series are gases; the high-molecular mass alkanes are waxy solid. Generaly the alkanes are fairly unreactive. They form haloalkanes with halogens when irradiated with ultraviolet radiation. Alkanes are present in natural gas and petroleum.

azo compounds    →   azo-spojevi

Azo compounds are organic compounds containing the group -N=N- linking two other groups. They can be formed by reaction of a diazonium ion with a benzene ring.

cation    →   kation

Cation is a positively charged atomic or molecular particle.

chalcogens    →   halkogeni elementi

Chalcogens are the Group 16 elements: oxygen (O), sulphur (S), selenium Se), tellurium (Te), and polonium (Po). Compounds of these elements are called chalcogenides.

charge number    →   nabojni broj

Charge number represents ion charge of an atom or a group. It is denoted as a right superscript (Fe²⁺ or SO₄^2-).

conjugated protein    →   konjugirani protein

Conjugated proteins are proteins which have a prostetic group as a part of their structure which is bonded with one or more amino acids of the same protein.

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.