Big Chemical Encyclopedia

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

Articles Figures Tables About

Hydrogen carbon—arsenic bond

A Ni-As(B) catalyst prepared by the borohydride reduction of alumina-supported nickel arsenate gave, on hydrogenation of 1-bromo-l 1-hexadecyne (13) in the presence of a small amount of acetone, a 97% yield of the alkene (14) having a 92 5 cis/trans ratio. No hydrogenolysis of the carbon-bromine bond occurred. "> 2 Borohydride reduction of cobalt acetate gave a Co(B) catalyst that was somewhat less active than Ni(B) but that was quite selective in alkyne semihydrogenations (Eqn. 16.20). ... [Pg.395]

In the first section of this chapter some of the properties of the elements hydrogen, carbon, nitrogen, phosphorus, arsenic, antimony, bismuth, oxygen, sulfur, selenium, tellurium, fluorine, chlorine, bromine, and iodine are described. The following sections are devoted to some of their compounds with one another, especially the single-bonded normal-valence compounds. Compounds of nonmetals with oxygen are discussed in the following chapter. [Pg.194]

From what has just been said with regard to carbon, it is evident that the atomicity of an element is, apparently at least, not a fixed and invariable quantity thus nitrogen is sometimes equivalent to five atoms of hydrogen, as in ammonic chloride, (i H Cl), sometimes to three atoms, as in ammonia (N" H,), mid sometimes to only one atom, as in nitrous oxide (N,0). But it is found that this variation in atomicity always takes place by the disappearance or development of an even number of bonds thus nitrogen is either a pentad, a triad, or a monad phosphorus and arsenic, either pentads or triads carbon and tin, either tetrads or dyads and sulphur, selenium, and tellurium, either hexads, tetrads, or dyads. [Pg.30]

The application of SPE has partially eliminated the above problems, particularly in the case of arsenic concentration in water samples [123]. SPE delivers better selectivity than LEE because it can be used to sequentially elute compounds from the activated carbon bed, and to separate inorganic compounds of As(III) and As (V), as well as the phenyl (PAS) and dimethyl (DMA) derivatives of arsenic (V) acid [124]. The extraction process is short, which is why it is possible to directly coimect the SPE module with the ICP MS detector [125]. Whenever modified silica is used, arsenic recovery is low (even below 50 %) owing to the formation of hydrogen bonds between the substances being separated and silanol groups [114, 126, 127]. [Pg.348]


See other pages where Hydrogen carbon—arsenic bond is mentioned: [Pg.16]    [Pg.200]    [Pg.133]    [Pg.272]    [Pg.167]    [Pg.167]    [Pg.200]    [Pg.200]    [Pg.136]    [Pg.267]    [Pg.242]    [Pg.913]    [Pg.328]    [Pg.5]    [Pg.3]    [Pg.319]    [Pg.1607]    [Pg.171]    [Pg.47]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.2 , Pg.2 , Pg.2 , Pg.3 , Pg.3 , Pg.3 , Pg.4 , Pg.4 , Pg.4 , Pg.4 , Pg.5 , Pg.5 , Pg.5 ]




SEARCH



Arsenic-carbon

Arsenic—carbon bonds hydrogen halides

Arsenic—hydrogen bonds

Bond carbon-arsenic

Carbon-hydrogen bonds

Hydrogen arsenate

© 2024 chempedia.info