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Addition compounds, inorganic

In addition to inorganic radicals, which profoundly modify the properties of a paraflSn hydrocarbon residue, there is a whole series of organic groupings which are distinguished by exceptional reactivity, for example, the ethylene and acetylene groupings, and the phenyl and naphthyl radicals. Thus the characterisation of unsaturated hydrocarbons and their derivatives, e.g., the aromatic compounds, becomes possible. [Pg.1026]

Reaction with Other Inorganic Halogen Compounds. Anhydrous HCl forms addition compounds at lower temperatures with halogen acids such as HBr and HI, and also with HCN. These compounds are stable at room temperature. [Pg.444]

In general, the chemistry of inorganic lead compounds is similar to that of the alkaline-earth elements. Thus the carbonate, nitrate, and sulfate of lead are isomorphous with the corresponding compounds of calcium, barium, and strontium. In addition, many inorganic lead compounds possess two or more crystalline forms having different properties. For example, the oxides and the sulfide of bivalent lead are frequendy colored as a result of their state of crystallisation. Pure, tetragonal a-PbO is red pure, orthorhombic P PbO is yeUow and crystals of lead sulfide, PbS, have a black, metallic luster. [Pg.67]

Aromatic amines form addition compounds and complexes with many inorganic substances, such as ziac chloride, copper chloride, uranium tetrachloride, or boron trifluoride. Various metals react with the amino group to form metal anilides and hydrochloric, sulfuric, or phosphoric acid salts of aniline are important intermediates in the dye industry. [Pg.229]

Addition compounds form with those organics that contain a donor atom, eg, ketonic oxygen, nitrogen, and sulfur. Thus, adducts form with amides, amines, and A/-heterocycles, as well as acid chlorides and ethers. Addition compounds also form with a number of inorganic compounds, eg, POCl (6,120). In many cases, the addition compounds are dimeric, eg, with ethyl acetate, in titanium tetrachloride-rich systems. By using ammonia, a series of amidodichlorides, Ti(NH2) Cl4, is formed (133). [Pg.131]

Nitrating cellulose with pure HNO is the simplest method of obtaining CN. In practice, nitration does not occur with acid concentrations below 75%. At acid concentrations <75%, an unstable compound (so called Knecht compound) is formed which has been described as a molecular complex or an oxonium salt of the nitric acid (72). HNO concentrations of 75—85% yield CN with 5—8% N, which dissolve in excess acid. CN with % N of 8—10% are formed at acid concentrations of 85—89%. Above 89%, a heterogeneous nitration occurs without apparent swelling of the cellulose fibers. CN with 13.3% N can be obtained with 100% HNO. Addition of inorganic salts to 100% HNO can raise the % N to 13.9. [Pg.268]

Senti and Witnauer206 have reported studies on the fiber diagrams from various alkali-amyloses. Specimens were obtained by deacetylating clamped specimens of amylose acetate with the appropriate alkali. The positions of the alkali ions and the lateral packing of the amylose chains were determined with the aid of Patterson projections. In the A - and B -modifica-tions, the fiber period was 22.6 A. (extension of 6 D-glucose units), whilst in the V -modification it was 8.0 A. These authors have also studied in detail the addition compounds of amylose and inorganic salts with special reference to the structure of the potassium bromide-amylose compound.206 Oriented alkali fibers were treated with the appropriate salt solution. Stoichiometric compounds were formed. The x-ray patterns from these showed that the addition compounds with potassium salts crystallized in... [Pg.379]

Hexacyanoferric(II) acid, ferrocyanic acid or tetrahydrogen hexakis(cyanate-(4-)) [17126-47-5] is used to prepare many adducts with oxygen-containing organics. Also addition compounds with inorganic salts are known. This acid may be obtained as a white precipitate upon addition of potassium ferrocyanide to concentrated hydrochloric acid ... [Pg.424]

Addition compounds of oxadiazoles with inorganic salts.835... [Pg.156]

Oxadiazole and its dervatives soluble in water form addition compounds with certain inorganic salts which precipitate from concentrated aqueous solutions of the respective salts. In particular, the halides of the metails of groups IB and IIB as well as those of Pt, Pd, precipitate adducts containing the metal and oxadiazole in 1 1 ratio. Under anhydrous conditions also adducts of AICI3 or BF3 were obtained (55b). [Pg.183]

As discussed in Chapter 2 and in more detail in Chapter 11, a variety of organic sulfur compounds in addition to inorganics such as H2S and COS are emitted by biological sources. In the troposphere, they may ultimately be oxidized to S02 and H2S04. However, the chemistry of these compounds tends to be complex, and a variety of partially oxidized sulfur compounds is formed first. [Pg.328]

Lubricant - [MOLYBDENUMAND COMPOUNDS] (Vol 16) -additives [SULFURIZATION AND SULFURCHLORINATION] (Vol 23) -barium as [BARIUM] (Vol 3) -bismuth compounds as [BISMUTH COMPOUNDS] (Vol 4) -boron nitride as [NITRIDES] (Vol 17) -boron tnfluonde as [FLUORINE COMPOUNDS,INORGANIC - BORON - BORON TRIFLUORIDE] (Vol 11) -ceriumcompdm [CERIUM AND CERIUM COMPOUNDS] (Vol 5) -glycerol as [GLYCEROL] (Vol 12) -hydrogenated terphenyls m [BIPHENYL AND TERPHENYLS] (Vol 4) -sodium tetrasulfidemmfg of [SODIUM COMPOUNDS - SODIUM SULFIDES] (Vol 22) -use of lime and limestone [LIME AND LIMESTONE] (Vol 15)... [Pg.579]

B. Additions of Inorganic Palladium Compounds I. Aqueous Palladium Chloride Reactions... [Pg.7]


See other pages where Addition compounds, inorganic is mentioned: [Pg.131]    [Pg.54]    [Pg.137]    [Pg.22]    [Pg.224]    [Pg.370]    [Pg.531]    [Pg.818]    [Pg.107]    [Pg.130]    [Pg.118]    [Pg.82]    [Pg.400]    [Pg.339]    [Pg.119]    [Pg.20]    [Pg.21]    [Pg.301]    [Pg.284]    [Pg.166]    [Pg.209]    [Pg.718]    [Pg.127]    [Pg.173]    [Pg.289]    [Pg.403]    [Pg.579]    [Pg.642]    [Pg.546]    [Pg.372]    [Pg.637]    [Pg.10]   
See also in sourсe #XX -- [ Pg.30 ]




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