CHEMISTRY GLOSSARY

Haber, Fritz    →   Haber, Fritz

Fritz Haber (1868-1934) is German physical chemist, winner of the Nobel Prize for Chemistry (1918) for his development of a method of synthesizing ammonia. With Carl Bosch, he invented a process for the large-scale production of ammonia for use in nitrogen fertilizer.

ether    →   eter

Ethers are organic compounds with a formula R-O-R, where R is not equal to H. They may be derived from alcohols by elimination of water, but the major method is catalytic hydration of olefins. They are volatile highly flammable compounds; when containing peroxides they can detonate on heating. The term ether is often used synonymously with diethyl ether.

extraction    →   ekstrakcija

Extraction is the separation of a component from its mixture by selective solubility. When a solution of one substance in one solvent is brought in with another solvent dissolved substance will distribute between the two solutants because of different solubility. Extraction is an efficient and fast method used for separating and concentrating matters. Extraction is best done several times in a succession, with smaller amount of solvent in it the matter is better dissolved. For example, caffeine can be separated from coffee beans by washing the beans with supercritical fluid carbon dioxide; the caffeine dissolves in the carbon dioxide, but flavour compounds do not. Vanillin can be extracted from vanilla beans by shaking the beans with an organic solvent, like ethanol.

fossil fuel    →   fosilno gorivo

Fossil fuels (coal, oil, and natural gas) are the fuels used by man as a source of energy. They are formed from the remains of living organisms and all have a high carbon or hydrogen content. They have value as fuels on the exothermic oxidation of carbon to form carbon dioxide

and the oxidation of hydrogen to form water

hemiacetal    →   poluacetal

Hemiacetals are organic compounds having the general formula R₂C(OH)OR’ (R’ ≠ H), derived from aldehydes or ketones by formal addition of an alcohol to the carbonyl group. Hemiacetals are generally unstable compounds. In some cases however, stable cyclic hemiacetals can be readily formed, especially when 5- and 6-membered rings are possible. In this case an intramolecular OH group reacts with the carbonyl group. Glucose and many other aldoses exist as cyclic hemiacetals whereas fructose and similar ketoses exist as cyclic hemiketals. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H).

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.

hemiketal    →   poluketal

Hemiketals are organic compounds having the structure R₂C(OH)OR (R ≠ H), derived from ketones by formal addition of an alcohol to the carbonyl group. The rings of ketose sugars are hemiketals. This term, once abandoned, has been reinstated as a subclass of hemiacetals.

magnetochemistry    →   magnetokemija

Magnetochemistry is a branch of physical chemistry which studies relations between magnetism and the chemical structure of matter.

Mannich reaction    →   Mannichova reakcija

Mannich reaction is a process in which hydrogen atoms in organic compounds are replaced with a methyl group.

mercaptans    →   merkaptani

Mercaptans are a traditional term abandoned by IUPAC, synonymous with thiols, a sulfur-containing organic compound with the general formula R-SH where R is any radical. This term is still widely used.