CHEMISTRY GLOSSARY

agarose    →   agaroza

Agarose is a polysaccharide obtained from agar that is used for a variety of life science applications especially in gel electrophoresis. The structure of agarose consists of alternating (1→3)-linked β-D-galactopyranose and (1→4)-linked 3,6-anhydro-α-L-galactopyranose.

aldehydes    →   aldehidi

Aldehydes are a broad class of organic compounds having the generic formula RCHO, and characterized by an unsaturated carbonyl group (C=O). They are formed from alcohols by either dehydrogenation or oxidation. Their chemical derivation is indicated by the name al(cohol) + dehyd(rogenation). An example of these distinct aromatic compounds is formaldehyde.

addition reactions    →   reakcije adicije

Addition reactions are normally occur with unsaturated compounds and involve the addition of one molecule (called the reactant) across the unsaturated bond (i.e. the double bond or the triple bond) of another molecule (called the substrate) to give a single product, formed by the combination of both reacting molecules.

For example, bromine adds across the double bond of ethene in an addition reaction to form dibromoethane.

aglycon    →   aglikon

Aglycon (aglycone) is the non-sugar compound remaining after replacement of the glycosyl group from a glycoside by a hydrogen atom. The link between the glycon and aglycon is known as glycosidic bond.

alcohol    →   alkohol

Alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom. Smaller members are water soluble, inflammable and are useful as organic solvents and fuels.

alkenes    →   alkeni

Alkenes are acyclic branched or unbranched hydrocarbons having one or more double carbon-carbon bonds in their molecules. In the systematic chemical nomenclature, alkene names end in the suffix -ene. The general formula is C_nH_(2n+2)-2x were x is the number of double bonds. Alkenes that have only one double bond form a homologous series: ethene (ethylene), CH₂=CH₂, propene, CH₃CH₂=CH₂, etc. Alkenes typically undergo addition reactions to the double bond.

amide    →   amid

Amide is an organic compound that contains a carbonyl group bound to nitrogen. The simplest amides are formamide (HCONH₂) and acetamide (CH₃CONH₂).

amines    →   amini

Amines are compounds formally derived from ammonia by replacing one, two, or three hydrogen atoms by hydrocarbyl groups, and having the general structures RNH₂ (primary amines), R₂NH (secondary amines), R₃N (tertiary amines). Examples are methylamine, CH₃NH₂; dimethylamine, CH₃NHCH₃; and trimethylamine, (CH₃)₃N.

amino acids    →   aminokiseline

Amino acids are compounds containing both a carboxylic acid group (-COOH) and an amino group (-NH₂ ). The most important are the α-amino acids, in which the -NH₂ group in attached to the C atom adjacent to the -COOH group. In the β-amino acids, there is an intervening carbon atom.

alkynes    →   alkini

Alkynes (acetylenes) are acyclic branched or unbranched hydrocarbons having one or more triple carbon-carbon bond. In the systematic chemical nomenclature alkyne names end in the suffix -yne. The general formula is C_nH_(2n+2)-4x were x is the number of triple bonds. Alkynes that have only one triple bond form a homologous series: ethyne (acetylene), CH≡CH, propyne, CH₃CH≡CH, etc. Like alkenes, alkynes undergo addition reaction.