CHEMISTRY GLOSSARY

lanthanides    →   lantanoidi

Lanthanides (lanthanons, lanthanoids or rare-earth elements) are a series of fourteen elements in the periodic table, generally considered to range in proton number from cerium to lutetium inclusive. It was convenient to divide these elements into the cerium group or light earth: cerium (Ce), praseodymium (Pr), neodymium (Nd), promethium (Pm), samarium (Sm), europium (Eu); and the yttrium group or heavy earths: gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb) i lutetium (Lu). The position of lanthanum is somewhat equivocal and, although not itself a lanthanide, it is often included with them for comparative purpose. The lanthanides are sometimes simply called the rare earths. Apart from unstable Pm, the lanthanides are actually not rare. Cerium is the 26. most abundant of all elements, 5 times as abundant as Pb. All are silvery very reactive metals.

lithium    →   litij

Lithium was discovered by Johan August Arfvedson (Sweden) in 1817. The origin of the name comes from the Greek word lithos meaning stone, apparently because it was discovered from a mineral source whereas the other two elements, sodium and potassium, were discovered from plant sources. It is soft silvery-white metal. Lightest of metals. Reacts slowly with water and oxygen. Flammable. Can ignite in air. Reacts with water to give off a flammable gas. Lithium is obtained by passing electric charge through melted lithium chloride and from the silicate mineral called spodumene [LiAl(Si₂O₆)]. Used in batteries. Also for certain kinds of glass and ceramics. Some is used in lubricants.

lysine    →   lizin

Lysine is an electrically charged amino acids with basic side chains. Lysine is a base, as are arginine and histidine. The amino group is highly reactive and often participates in reactions at the active centers of enzymes. Lysine plays an important role in coordinating negatively charged ligands. It is an essential amino acid, which means that humans cannot synthesize it, so it must be ingested.

• Abbreviations: Lys, K
• IUPAC name: 2,6-diaminohexanoic acid
• Molecular formula: C₆H₁₄N₂O₂
• Molecular weight: 146.19 g/mol

meta position    →   meta položaj

Meta position in organic chemistry is the one in which there are two same functional groups tied to a ring of benzene in position 1 and 3. The abbreviation m- is used, for example, m-Hydroquinone is 1,3-dihydroxybenzene.

methionine    →   metionin

Methionine is neutral amino acids with polar side chains. It is one of the two sulfur-containing amino acids. Methionine is a fairly hydrophobic amino acid and typically found buried within the interior of a protein. It can form stacking interactions with the aromatic moieties of tryptophan, phenylalanine, and tyrosine. It is an essential amino acid, which means that humans cannot synthesize it, so it must be ingested.

• Abbreviations: Met, M
• IUPAC name: 2-amino-4-methylsulfanylbutanoic acid
• Molecular formula: C₅H₁₁NO₂S
• Molecular weight: 149.21 g/mol

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.

noble gas    →   plemeniti plin

Noble gas refers to any element of the group of six elements in group 18 of the periodic table. They are helium (He), neon (Ne), argon (Ar), krypton (Kr), xenon (Xe), and radon (Rn). Unlike most elements, the noble gases are monoatomic. The atoms have stable configurations of electrons. Therefore, under normal conditions they do not form compounds with other elements.

They were generally called inert gases until about 1962 when xenon tetrafluoride, XeF₄, was produced in the laboratory. This was the first report of a stable compound of a noble gas with another single element.

nucleotide    →   nukleotid

Nucleotides are the components that made up nucleic acids. They have three major components: the first component is a nitrogenous base, which is derivative of one of two parent compounds, pyrimidine or purine; the second is a pentose, or five carbon sugar group; the third is a unit of phosphate. Each group of three nucleotides in a gene is known as a codon. Whenever the phosphate group is not present, a nucleotide becomes a nucleoside.

ortho position    →   ortho položaj

Ortho position in organic chemistry is the one in which there are two same functional groups, tied to a ring of benzene in the positions 1 and 2. The abbreviation o- is used, for example, o-Hydroquinone is 1,2-dihydroxybenzene.

osmium    →   osmij

Osmium was discovered by Smithson Tennant (England) in 1803. The origin of the name comes from the Greek word osme meaning smell. It is hard fine black powder or hard, lustrous, blue-white metal. Unaffected by air, water and acids. Characteristic acrid, chlorine like odour due to tetroxide compound. Osmium tetroxide highly toxic. Osmium is obtained from the same ores as platinum. Used to tip gold pen points, instrument pivots, to make electric light filaments. Used for high temperature alloys and pressure bearings. Very hard and resists corrosion better than any other.