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Iodine, 48-49 making

Because of their low polarizability, BF3 and BCI3 are gases. The larger, more polarizable electron clouds on bromine and iodine make BBt3 a volatile liquid and BI3 a solid at room temperature. [Pg.1522]

More importantly, the addition of iodine makes it possible to operate the filament at a hotter temperature, with a higher proportion of the emitted light being visible light, although we still form much heat. [Pg.475]

Iodine makes blue colored complexes with many substances such as starch [1, 2] nylon-6 [3], poly(vinyl pyrrolidone) [4], poly(vinyl alcohol) PVA [5, 6], From the application point of view, the blue PVA-Iodine complex is the most important among them, for it is widely used for film polarizers [7,8]. The polarizers are prepared by soaking PVA films in a solution of iodine and potassium iodide (KI) with boric acid, and subsequent drawing to cause the high... [Pg.91]

The weakly electrophilic properties of iodine make it a mild Lewis acid with potential for selective cleavage of silyl ethers as shown in Scheme 4,42.M... [Pg.211]

While etbyliodoacetate was one of the most powerful lacrimators used in the war, the Britbh were forced to adopt it because of a shortage of bromine and the fact that they then had access to large supplies of iodint from South America. At the present time, the price and scarcity of iodine make the future use of thb compound as a chemical agent undesir-... [Pg.211]

One of the four bonds of the carbon is left free. In methane this free bond is satisfied by another hydrogen atom in methyl chloride or iodide by one of chlorine or iodine, making in each case a saturated cornpound. When, therefore, two molecules of methyl iodide each lose their iodine to zinc or sodium we have left the two methyl radicals with this fourth valence of each carbon unsatisfied. These two free valencies satisfy each otherj and we have the two methyl radicals united just as we believe two free atoms unite to form a molecule. We may write the reaction then ... [Pg.16]

Analysis of the TBPA-Ti complex (39,40) indicates that the binding site for the hormone is located deep inside the channel. The hormone makes extensive interactions with the protein side chains that project into the channel. The 4 -hydroxyl of Ti interacts with a patch of hydroxy-amino acids of the protein while each of the iodines makes contact with a number of hydro-phobic protein residues. The T amino acid side chain functional groups are in appropriate positions to interact with glutamic acid and lysine residues. Thus, this channel provides a favorable environment for each of the characteristic substituents of the thyroid hormone (40). However, because of the Ti orientation disorder in the protein complex, this structural model is not a sensitive measure of the observed correlations between diphenyl ether conformations and binding affinity data. [Pg.293]

Nor does the fact that, according to Gunther s experiments (cf. p. 53), somewhat different values should be used for the atomic heat of iodine, make much difference. By using the new table calculated by Frl. Miething (p. 97), the result is as follows —... [Pg.115]

Supplements. Potassium iodide is available as a nutritional supplement, typically in combination products, such as multivitamin/multimineral supplements. Iodine makes up approximately 77% of the total weight of potassium iodide. ° Potassium iodide as well as potassium iodate may be used to iodize salt. Iodized vegetable oil is also used in some countries as an iodine source. °- ... [Pg.268]

A more convenient variation on this method is to combine 50 grams of silica gel with about 200 mg of iodine crystals in an 8-oz. jar. Rotate the jar periodically to disperse the iodine. Making certain that the TLC plate is completely dry, immerse it in the silica gel-iodine mixture and close the lid tightly. Rotate the jar to ensure that the TLC plate is completely covered. After one or two minutes, remove the plate from the jar using forceps. Be careful not to inhale the powder ... [Pg.818]

FIGURE 19.36 The initially formed a-iodo carbonyl compound is a stronger acid than the carbonyl compound itself. The introduced iodine makes enolate formation easier. [Pg.948]

This anion reacts in Sn2 fashion with iodine to generate the a-iodo carbonyl compound. Now, however, the electron-withdrawing inductive effect of iodine makes enolate formation easier, not harder, as for enols. The negative charge of the enolate is stabilized by the electron-withdrawing effect. A second and third displacement reaction on iodine generates the a,a,a-triiodo carbonyl compound (Fig. 19.37). Similar reactions are known for bromine and chlorine. [Pg.948]

The presence of chloric(I) acid makes the properties of chlorine water different from those of gaseous chlorine, just as aqueous sulphur dioxide is very different from the gas. Chloric(I) acid is a strong oxidising agent, and in acid solution will even oxidise sulphur to sulphuric acid however, the concentration of free chloric(I) acid in chlorine water is often low and oxidation reactions are not always complete. Nevertheless when chlorine bleaches moist litmus, it is the chloric(I) acid which is formed that produces the bleaching. The reaction of chlorine gas with aqueous bromide or iodide ions which causes displacement of bromine or iodine (see below) may also involve the reaction... [Pg.323]

Iodine has the lowest standard electrode potential of any of the common halogens (E = +0.54 V) and is consequently the least powerful oxidising agent. Indeed, the iodide ion can be oxidised to iodine by many reagents including air which will oxidise an acidified solution of iodide ions. However, iodine will oxidise arsenate(lll) to arsenate(V) in alkaline solution (the presence of sodium carbonate makes the solution sufficiently alkaline) but the reaction is reversible, for example by removal of iodine. [Pg.326]

In water pollution studies, the oxygen content can be measured by making the water alkaline and shaking a measured volume with an oxygen-free solution containing Mn- (aq). The solution is acidified with sulphuric acid, potassium iodide added and the liberated iodine titrated with sodium thiosulphate. [Pg.389]

The plate is removed from the tank, the position of the solvent front marked, and the solvent allowed to evaporate from the plate. If the components of the mixture are coloured, the separation is obvious if colourless, they must be located either by viewing under U.. or by standing the plate in a closed dry tank containing crystals of iodine, whose vapour makes brown spots show i p. [Pg.58]

One need not inhibit oneself by using HBr. One can use Nal or Kl to make HI which is even better than HBr in any of these recipes. Iodine adds much better and swaps out with the amines much better. Yield are much higher The other thing to notice is that reaction carries itself out in DMSO. Seems logical to believe that one could bubble their HBr gasses into this solvent instead of acetic acid. [Pg.148]

Many artificial (likely radioactive) isotopes can be created through nuclear reactions. Radioactive isotopes of iodine are used in medicine, while isotopes of plutonium are used in making atomic bombs. In many analytical applications, the ratio of occurrence of the isotopes is important. For example, it may be important to know the exact ratio of the abundances (relative amounts) of the isotopes 1, 2, and 3 in hydrogen. Such knowledge can be obtained through a mass spectrometric measurement of the isotope abundance ratio. [Pg.423]

Approximately half of the iodine consumed is used to make potassium iodide (see Iodine and iodine compounds). Production of KI is almost 1000 t/yr. Its main uses are in animal and human food, particularly in iodized salt, pharmaceuticals (qv), and photography (qv). [Pg.534]


See other pages where Iodine, 48-49 making is mentioned: [Pg.405]    [Pg.311]    [Pg.344]    [Pg.232]    [Pg.311]    [Pg.344]    [Pg.709]    [Pg.150]    [Pg.403]    [Pg.148]    [Pg.45]    [Pg.818]    [Pg.123]    [Pg.181]    [Pg.166]    [Pg.91]    [Pg.315]    [Pg.50]    [Pg.846]    [Pg.3]    [Pg.106]    [Pg.254]    [Pg.286]    [Pg.814]    [Pg.131]    [Pg.132]    [Pg.1197]    [Pg.343]    [Pg.103]    [Pg.404]    [Pg.68]    [Pg.505]   
See also in sourсe #XX -- [ Pg.48 , Pg.49 ]




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