Results 621–630 of 1083 for Startseite Charts Anmelden Tools Schlagw%F6rter Mitgliederbereich language:en
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.
Glycoside is one of a group of organic compounds in which a sugar group is bonded through its anomeric carbon to another group via a glycosidic bond. The sugar group is known as the glycon and the non-sugar group as the aglycon. According to the IUPAC definition, all disaccharides and polysaccharides are glycosides where the aglycone is another sugar.
In the free hemiacetal form, sugars will spontaneously equilibrate between the α and β anomers. However, once the glycosidic bond is formed, the anomeric configuration of the ring is locked as either α or β. Therefore, the alpha and beta glycosides are chemically distinct. They will have different chemical, physical, and biological properties. Many glycosides occur abundantly in plants, especially as flower and fruit pigments.
The term glycoside was later extended to cover not only compounds in which the anomeric hydroxy group is replaced by a group -OR, but also those in which the replacing group is -SR (thioglycosides), -SeR (selenoglycosides), -NR1R2 (N-glycosides), or even -CR1R2R3 (C-glycosides). Thioglycoside and selenoglycoside are legitimate generic terms; however the use of N-glycoside, although widespread in biochemical literature, is improper and not recommended here (glycosylamine is a perfectly acceptable term). C-Glycoside is even less acceptable. All other glycosides are hydrolysable; the C-C bond of C-glycosides is usually not. The use and propagation of names based on C-glycoside terminology is therefore strongly discouraged.
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.
Neutron number (N) is a characteristic property of a specific isotope of an element, equal to the number of neutrons in the nucleus.
Nonelectrolytes are substances which in solutions do not dissociate into ions and they do not conduct electric current.
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.
Generalic, Eni. "Startseite Charts Anmelden Tools Schlagw%F6rter Mitgliederbereich language:en." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. {Date of access}. <https://glossary.periodni.com>.
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