CHEMISTRY GLOSSARY

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.

alicyclic    →   aliciklički spojevi

Alicyclic compounds are aliphatic compounds with a ring of atoms. They have C_nH_2n general formula (e.g. cyclohexane C₆H₁₂).

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.

diazo compounds    →   diazo-spojevi

Diazo compounds are compounds having the divalent diazo group, =N⁺=N^-, attached to a carbon atom. The term includes azo compounds, diazonium compounds, and also such compounds as diazomethane, CH₂=N₂.

alkaloid    →   alkaloid

Alkaloids are basic nitrogen organic compounds (mostly heterocyclic) derived from plants and having diverse pharmacological properties. Alkaloids include morphine, cocaine, atropine, quinine, and caffeine, most of which are used in medicine as analgesics or anaesthetics. Some alkaloids are poisonous, e.g. strychnine and coniine, and colchicine inhibit cell division.

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.

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.

abundance of elements    →   rasprostranjenost elemenata

Elements in nature are mostly found in different compounds and, rarely, in the free (elementary) state. In Earth’s crust the most abundant of all elements is oxygen (with 49.5 %), then silicon (25 %), aluminium (7.5 %), iron (4.7 %), calcium (3.4 %), sodium (2.6 %), potassium (2.4 %), magnesium (1.9 %) and hydrogen (1.9 %). These nine elements make up almost 99 % of the Earth’s composition.

acceptor    →   akceptor

Acceptor is a compound, molecule or ion, to which electrons are donated in the formation of a coordinate bond

acetal    →   acetal

Acetals are organic compounds having the structure R₂C(OR’)₂ (R’ ≠ H). They are organic compounds formed by addition of alcohol molecules to aldehyde or ketone molecules. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H ). Mixed acetals have different R’ groups. The formation of acetals is reversible; acetals can be hydrolysed back to aldehydes (ketone) in acidic solutions.

Acetal, 1,1-diethoxyethane (CH₃CH(OC₂H₅)₂), is an organic compound, pleasant smelling, formed by addition of ethyl alcohol to ethanal (acetaldehyde). It is used as a solvent and in synthetic organic chemistry.