CHEMISTRY GLOSSARY

ringlike structure    →   prstenasta struktura

The ringlike structure is a structure by which the cycloalcanes and aromates are shown.

Lewis structure    →   Lewisova struktura

Lewis structure is the representation of the electron arrangement in atoms, ions, or molecules by showing the valence electrons as dots placed around the symbols for the elements.

planary structure    →   planarna struktura molekule

Planary structure of molecule is a structure of molecule in which all atoms in the molecule lie in the same plane.

primary structure of proteins    →   primarna struktura proteina

Primary structure of proteins is a sequence of defined amino acids in some protein.

condensed structural formulas    →   kondenzirane strukturne formule

Condensed structural formulas are shortened and easier layout of structural formulas of organic compounds (butane, CH₃(CH₂)₂CH₃).

structural isomer    →   strukturni izomer

Structural isomers are compounds that have the same formula, but different constituents. Dimethyl ether (CH₃OCH₃) and ethanol (CH₃CH₂OH), for example, are constitutional isomers with general formula C₃H₆O.

structural formula    →   strukturna formula

Structural formula is a two dimensional representations of the arrangement of the atoms in molecules. Atoms are represented by their element symbols and covalent bonds are represented by lines. The symbol for carbon is often not drawn.

chain    →   lanac

Chain is a linear combination of the same type of atom in a molecule. In straight chain molecules, the atoms are arranged in a line, with each atom in the chain linked to one preceding atom and one succeeding atom of the same type. A closed chain molecule is a chain where the atoms are linked in a ring structure.

chelate    →   kelat

Chelate is a compound characterized by the presence of bonds from two or more bonding sites within the same ligand to a central metal atom. For example, copper complexes with EDTA to form a chelate. Chelate complexes are more stable than complexes with the corresponding monodentate ligands.

monosaccharide    →   monosaharid

Monosaccharides are carbohydrates, with the general formula C_n(H₂O)_n, that cannot be decomposed to a simpler carbohydrates by hydrolysis.

Depending on whether the molecule contains an aldehyde group (-CHO) or a ketone group (-CO-) monosaccharide can be a polyhydroxy aldehyde (aldose) or a polyhydroxy ketone (ketose). These aldehyde and ketone groups confer reduction properties on monosaccharides. They are also classified according to the number of carbon atoms they contain: trioses have three carbon atoms, tetroses four, pentoses five, hexoses six, heptoses seven, etc. These two systems of classification are often combined. For example, a six-carbon polyhydroxy aldehyde such as D-glucose is an aldohexose, whereas a six-carbon polyhydroxy ketone such as D-fructose is a ketohexose.

The notations D and L are used to describe the configurations of carbohydrates. In Fischer projections of monosaccharides, the carbonyl group is always placed on top (in the case of aldoses) or as close to the top as possible (in the case of ketoses). If the OH group attached to the bottom-most asymmetric carbon (the carbon that is second from the bottom) is on the right, then the compound is a D-sugar. If the OH group is on the left, then the compound is an L-sugar. Almost all sugars found in nature are D-sugars.

Monosaccharides can exist as either straight-chain or ring-shaped molecules. During the conversion from straight-chain form to cyclic form, the carbon atom containing the carbonyl oxygen, called the anomeric carbon, becomes a chiral center with two possible configurations (anomers), α and β. When the stereochemistry of the first carbon matches the stereochemistry of the last stereogenic center the sugar is the α-anomer when they are opposite the sugar is the β-anomer.