Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Principal compounds

Intermetallic Compounds. Numerous intermetalhc galhum—transition element compounds have been reported (17). The principal compounds ate hsted in Table 4 (18—23). There ate probably several Cs and Rb compounds however, none is well known. [Pg.160]

The principal compounds in this category are the monochalacogenides, which are formed by all three metals. It is a notable indication of the stability of tetrahedral coordination for the elements of Group 12 that, of the 12 compounds of this type, only CdO, HgO and HgS adopt a structure other than wurtzite or zinc blende (both of which involve tetrahedral coordination of the cation — see below). CdO adopts the 6-coordinate rock-salt structure HgO features zigzag chains of almost linear O-Hg-0 units and HgS exists in both a zinc-blende form and in a rock-salt form. [Pg.1208]

The alkanes are the principal compounds present in natural gas and in petroleum. The low molecular weight compounds are gases under... [Pg.341]

Describe the names, properties, and reactions of the principal compounds of hydrogen and the Period 1 through 3 elements in Groups 1, 2, 13/III, and 14/IV. [Pg.738]

All of Hamao U mezawa s work was closely connected with carbohydrates. The principal compounds that he developed, namely, kanamycin, dibekacin (with the elucidation of the resistance mechanism), kasugamycin, formycin, bleomycin, and anthracyclines, are all glycosides. The l.m.w. enzyme-inhibitors, exemplified by bestatin, are mostly oligopeptides, and are the only exceptions. [Pg.16]

Among the wide and varied types of compounds that are reduced to metals, the oxides are by far the most extensively encountered entities. Metal oxides, in forms amenable to reduction, occur either as principal compounds in ores or can be readily obtained from other compounds that occur in the ores. Many reducing agents are available for converting the oxides to the metal. [Pg.359]

This is an analytical technique used to obtain accurate quantification of the principal compound constituents such as plasticiser, polymer, carbon black and inorganic species, by monitoring weight loss across a temperature range. [Pg.65]

Standards used for the construction of calibration curves had alkyl chain lengths in the range Ci6 to C19. Table 9.2 gives the principal compounds used as representatives of each class. [Pg.426]

Principal Compounds Rhodium trichloride rhodium trioxide rhodium (II) acetate rhodium nitrate rhodium potassium sulfate rhodium sulfate rhodium sulfite... [Pg.618]

The element was synthesized in 1950 by S. G. Thompson, A. Ghiorso, K. Street, and Glen T. Seaborg, It was named after the state of California. Californium does not occur in nature. It can be synthesized only in microgram amounts in a nuclear reactor. The principal compounds of the element that have been synthesized are the cahfomium trifluoride, CfFs californium trichloride, CfCls californium oxide, Cf203 californium oxychloride Cf(OCl)3 and cahfomium hydroxide Cf(OH)3. The element has not yet been obtained in metalhc state. [Pg.179]

The following ore the names and formula of the principal compounds of this metal —... [Pg.104]

More than 350 volatile compounds have been identified in apples [44]. Only a few of these volatiles have been identified as being responsible for apple aroma [45]. The most abundant volatile components in apples are esters (78-92% of total volatiles), alcohols (6-16% of total volatiles), aldehydes, ketones and ethers [35, 45], which are present in various amounts in different cultivars [46]. Esters are the principal compounds responsible for apple odour (Table 7.1, Fig 7.1)... [Pg.145]

Osmium has little tendency to simple salt formation owing to the great affinity which the element has for oxygen. The principal compounds, therefore, are complex in character. The ammino-derivatives appear to be derived from the two ammino-bases, 10s0(NH.)J(0H), and [0s02(NH3)4](0H)3. [Pg.214]

Riboflavin absorbs light maximally at about 450nm and in doing so can be excited to a triplet state. This excited form of riboflavin can interact with triplet 02 to form a superoxide anion OJ (or H202 at low pH). Excited riboflavin can also oxidize ascorbate, a number of amino acids and proteins and orotic acid. Riboflavin-catalysed photo-oxidation results in the production of a number of compounds, most notably methional (11.1) which is the principal compound responsible for the off-flavour in milk exposed to light. [Pg.362]

Many of the principal compounds of strontium and barium which could have been present in the sediment are also soluble in water, but the carbonates and sulfates are relatively insoluble. [Pg.270]

The parsley plant, Petroselinum crispum, for example, contains at least two of the D-apiose flavonoids, namely, apiin 4, 5-dihydroxy-flavon-7-yl 2-0- [3-C (hydroxymethyl)-/3-D-erythrofuranosyl] -/3-D-glucopyranoside (4) and petroselinin 3, 4, 5-trihydroxyflavon-7-yl 2-0- [3-C-(hydroxymethyl)-/3-D-erythrofuranosyl]-/3-D-glucopyrano-side. 1 The principal compound containing D-apiose in parsley... [Pg.140]

The wine yeast, Saccharomyces fermentati, is able to form a film or veil on the surface of dry white wines of about 15-16% alcohol. This yeast produces agreeable smelling and tasting substances which dissolve in the wine and give it the aroma and flavor characteristic of Spanish fino sherries. To provide itself with energy for growth while in the film form on the surface of the wine, the yeast utilizes some of the oxygen from the atmosphere above the wine in the partially filled butt or barrel to oxidize some of the ethyl alcohol from the wine. The ethyl alcohol of the wine is not completely metabolized to carbon dioxide and water, however, but is oxidized to acetaldehyde—probably the principal compound in the complex mixture responsible for the aroma of this type of appetizer wine. [Pg.306]


See other pages where Principal compounds is mentioned: [Pg.205]    [Pg.249]    [Pg.37]    [Pg.224]    [Pg.387]    [Pg.203]    [Pg.284]    [Pg.438]    [Pg.323]    [Pg.339]    [Pg.652]    [Pg.66]    [Pg.770]    [Pg.812]    [Pg.314]    [Pg.168]    [Pg.205]    [Pg.31]    [Pg.85]    [Pg.526]    [Pg.121]    [Pg.170]    [Pg.339]    [Pg.335]    [Pg.557]    [Pg.964]    [Pg.1159]    [Pg.323]    [Pg.9]    [Pg.339]    [Pg.203]   
See also in sourсe #XX -- [ Pg.190 , Pg.206 ]




SEARCH



© 2024 chempedia.info