Glycosidic bond ia a bond between the glycosyl group, the structure obtained by removing the hydroxy group from the hemiacetal function of a monosaccharide, and the -OR group (which itself may be derived from a saccharide and chalcogen replacements thereof (RS–, RSe–). The terms N-glycosides and C-glycosides are misnomers and should not be used. The glycosidic bond can be α or β in orientation, depending on whether the anomeric hydroxyl group was α or β before the glycosidic bond was formed and on the specificity of the enzymatic reaction catalyzing their formation. Once the glycosidic bond is formed, the anomeric configuration of the ring is locked as either α or β. Specific glycosidic bonds therefore may be designated α(1→4), β(1→4), α(1→6), and so on. Cellulose is formed of glucose molecules linked by β(1→4)-glycosidic bonds, whereas starch is composed of α(1→4)-glycosidic bonds.
Gold has been known since ancient times. The origin of the name comes from the Latin word aurum meaning gold. It is soft, malleable, bright yellow metal. Unaffected by air, water, alkalis and most acids. Gold is found in veins in the crust, with copper ore and native. Used in electronics, jewellery and coins. It is a good reflector of infrared radiation, so a thin film of gold is applied to the glass of skyscrapers to reduce internal heating from sunlight.
Goldschmidt process (thermite process) is a method of extracting metals by reducing the oxide with aluminium powder. Practically all the metallic oxides are reducible by this method, the chief exception being the oxide of magnesium. The thermite process was developed by the German chemist Hans Goldschmidt (1861-1923) in 1893.
Goldschmidt was originally interested in producing very pure metals, but he soon realized the value in welding, a process known as Thermit welding.
Graduated pipettes (Mohr pipette) have a scale divided into units of one and of 1/10th of a millilitre. Because of their wide necks it is less accurate than the volumetric pipette. They are used when taking volume of solutions in which accuracy does not have to be very high. By sucking in (with mouth, propipette or a water pump) the liquid is pulled in a little bit above the mark and the opening of the pipet is closed with a forefingertip. Outer wall of pipet is wiped and, with a slight forefinger loosening, the liquid is released until it reaches the mark 0. A pipette is emptied out by lifting the forefinger off and letting the liquid flow out of the pipette freely.
Graham’s law is the rates at whish gases diffuse are inversely proportional to the square roots of their densities. This principle is made use of in the diffusion method of separating isotopes. The law was formulated in 1829 by British chemist Thomas Graham (1805-1869).
Graphite is an allotrope of carbon. The atoms are arranged in layers as a series of flat, hexagonal rings. Graphite is a good conductor of heat and electricity. The layers cleave easily, making graphite useful as a solid lubricant. A process to make pure synthetic graphite was invented by the American chemist Edward Goodrich Acheson (1856–1931). The process consists of heating a mixture of clay (aluminum silicate) and powdered coke (carbon) in an iron bowl. The reaction involves the production of silicon carbide, which loses silicon at 4150 °C to leave graphite.
Grätzel solar cell is photoelectrochemical cell, developed by Michael Grätzel and collaborators, simulates some characteristics of the natural solar cell, which enables photosynthesis take place. In natural solar cell the chlorophyll molecules absorb light (most strongly in the red and blue parts of the spectrum, leaving the green light to be reflected). The absorbed energy is sufficient to knock an electron from the excited chlorophyll. In the further transport of electron, other molecules are involved, which take the electron away from chlorophyll. In Grätzel cell, the tasks of charge-carrier generation and transport are also assigned to different species.
His device consists of an array of nanometre-sized crystallites of the semiconductor titanium dioxide, welded together and coated with light-sensitive molecules that can transfer electrons to the semiconductor particles when they absorb photons. So, light-sensitive molecules play a role equivalent to chlorophyll in photosynthesis. In Grätzel cell, the light-sensitive molecule is a ruthenium ion bound to organic bipyridine molecules, which absorb light strongly in the visible range; titanium dioxide nanocrystals carry the received photoexcited electrons away from electron donors. On the other hand, a donor molecule must get back an electron, so that it can absorb another photon. So, this assembly is immersed in a liquid electrolyte containing molecular species (dissolved iodine molecules) that can pick up an electron from an electrode immersed in the solution and ferry it to the donor molecule. These cells can convert sunlight with efficiency of 10 % in direct sunlight and they are even more efficient in diffuse daylight.
Gravimetry is the quantitative measurement of an analyte by weighing a pure, solid form of the analyte. Since gravimetric analysis is an absolute measurement, it is the principal method for analysing and preparing primary standards.
A typical experimental procedure to determine an unknown concentration of an analyte in a solution is as follows:
- quantitatively precipitate the analyte from the solution
- collect the precipitate by filtering and wash it to remove impurities
- dry the solid in an oven to remove the solvent
- weigh the solid on an analytical balance
- calculate the analyte concentration in the original solution based on the weight of the precipitate.
Periodic system of elements is divided into 18 groups of chemical elements. Elements belonging to the same group have a same number of valence electrons and similar chemical properties. Elements of main groups are in 1., 2., and in groups 13. to 18. Different groups of elements can be named according to the first element in the group (elements of boron group, elements of carbon group), or they have some special names (noble gases, halogenic elements, halyde elements, earthalkali and alkali metals).
Haber process is an industrial process for producing ammonia by reaction of nitrogen with hydrogen:
The reaction is reversible and exothermic, so that a high yield of ammonia is favoured by low temperature. However, the rate of reaction would be too slow for equilibrium to be reached at normal temperatures, so an optimum temperature of about 450 °C is used, with a catalyst of iron containing potassium aluminium oxide promoters. The higher the pressure the greater the yield, although there are technical difficulties in using very high pressures. A pressure of about 250 atmospheres is commonly employed. The removal of ammonia from the batch as soon as it is formed ensures that an equilibrium favouring product formation is maintained. The nitrogen is obtained from air. Formerly, the hydrogen was from water gas and the water-gas shift reaction (the Bosch process) but now the raw material (called synthesis gas) is obtained by steam reforming natural gas.
The process is of immense importance for the fixation of nitrogen for fertilisers and explosives. It was developed in 1908 by German chemist Fritz Haber (1868-1934) and was developed for industrial use by Carl Bosch (1874-1940), hence the alternative name Haber-Bosch process.
Generalic, Eni. "OFICINAVIRTUAL.ISSSTE.GOB.MX." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. {Date of access}. <https://glossary.periodni.com>.
Glossary
Periodic Table