Ammonium bromide chlorides from iodide

Conversion of the organotin chlorides into fluorides, bromides, or iodides is usually carried out with the sodium halide in acetone, and residual organotin compounds are often removed as the insoluble organotin fluorides. The fluorides can then be converted back into the bromides, chlorides, or iodides (and exchanges by other halides can be brought about with aqueous ammonium halides at room temperature).332 A 2 1 mixture (solid solution) of CsF and CsOH, mixed with silica gel, also provides a very convenient way of removing organotin halide byproducts from solution.333... 

According to F. C. Franklin and C. A. Kraus,40 liquid ammonia readily dissolves sodium and potassium iodides. The partial press, of ammonia in soln. of potassium iodide at 25°, as measured by R. Abegg and H. Riesenfeld, is raised from 13 45 mm. of water to 13 28, and 14 88 mm. for 0 5W-, N-, and l 5Ar-soln. respectively. H. M. Dawson and J. McCrae have shown that the distribution of ammonia between water and chloroform is generally lowered by the addition of various salts of the alkali metals and ammonium which they tried—halides, nitrates, chlorates, oxalates, sulphates, carbonates, hydroxides this means that the solvent power of aq. soln. of the alkali salts is in general less than that of pure water—lithium chloride, ammonium bromide, and sodium iodide act in the opposite way. The other halide salts of lithium were not tried. The change produced in the partition coeff. by the halides, at 20°, is as follows ... 

The heat of formation of ammonium chloride from the elements is 317 kJ /mol (75.8 kcal/mol) it is 175 kJ /mol (41.9 kcal/mol) from gaseous ammonia and gaseous hydrogen chloride. The heat of formation of ammonium bromide from the elements, bromine in the Hquid form, is 273 kJ /mol (65.3 kcal/mol) for ammonium iodide, the corresponding heat of formation is 206 kJ /mol (49.3 kcal/mol). Iodine is in the soHd state. 

When Berthier treated a specimen of this ore from the San Onofe Mine with an excess of hot ammonium hydroxide, he observed, mixed with the metallic silver, a green powder which had been only incompletely attacked. This was the circumstance, said he, which drew my attention to the ore from Plateros and which led me to realize that the substance which had been taken for silver chloride is pure bromide, without admixture of chloride or iodide, a substance which had not yet been met within the mineral realm and which therefore constitutes a new species (151). Berthier learned that this mineral is not rare in Mexico but is often found in beautiful cubic and octahedral crystals. He also found the same mineral at Huelgoeth, Department of Finistere, France, and discovered some of it among the Chilean silver minerals which Ignaz Domeyko, professor of chemistry at the College of Coquimbo, had sent to the School of Mines at Paris (151, 152). The mineral which Berthier analyzed was evidently bromyrite (silver bromide). 

The reported specific gravity of ammonium iodide 3 ranges from H. G. F. Schroder s 2 443 to H. Schifi and U. Monsacchi s 2"5168 (15°). The best representative value may be taken as 2-511. The molecular volumes of the ammonium halides come between those of rubidium and caesium halides for example, ammonium chloride, 34-01 ammonium bromide, 39 62 ammonium iodide, 57 51. W. Biltz has also studied the mol. vol. of this salt. 

Although several systems have been evaluated to determine the structure of the ring formed in cyclopolymerization, very little work has been reported on the original cyclopolymer reported by Butler ( 7) that was obtained from N,N-dimethyldiallyl-ammonium bromide or the chloride. Consequently, we undertook a study of a five-membered quaternary ammonium polymer, poly(l,l, 3,4-tetramethyl-3-pyrrolinium bromide) as a model system. N,N-dimethyl-3,4-dimethylenepyrrolidinium bromide (6 ) was prepared by reacting dimethylamine with 2,3-bis(bromomethyl)-l,3-butadiene (5). In addition to the bromide salt (6), the iodide salt was also prepared by reacting 2,3-bis(bromomethyl)-l,3-butadiene... 

Mercury diphenyl has been prepared in a number of ways. The most important methods are by the action of sodium on a mixture of bromobcnzene and mercuric chloride from sodium amalgam and phenyl mercuric iodide 2 by the interaction of phenyl mercuric bromide and potassium sulfide2 or phenyl mercuric acetate and sodium stannite 3 from phenyl magnesium bromide and mercuric chloride 4 by the action of phenyl hydrazine on mercury compounds 5 from mercuric chloride and phenyl arsenious oxide 6 and from diphenyl mercuric ammonium acetate and sulfur compounds.7... 

We saw that in an E2 reaction of an alkyl chloride, alkyl bromide, or alkyl iodide, a hydrogen is removed from the j8-carbon bonded to the fewest hydrogens (Zaitsev s rule, Section 11.2). Now we see that in an E2 reaction of a quaternary ammonium ion, the hydrogen is removed from the j8-carbon bonded to the most hydrogens (anti-... 

E. coli and S. aureus Some quinuclidinium compounds were quite active in vitro with the most active XVIII having MIC values of 0.4 ug/ml for S. aureus and B. subtilis. A group of 68 N,N-dimethyl-N-alkyl-2-aryloxyethyl ammonium bromides were prepared and screened vs 8 common infectious organisms, and the best had alkyl groups of from 8-12 carbon atoms, with MIC values as low as 0.5 yg/ml. Bis-quaternary salts of ethylene and hexamethylene diamine of type XIX were active in vitro . The most active had R=CioH2i and the chloride had greater activity than the corresponding iodide. Another paper dealt with the structure-activity relationships of compounds of type XIX . Various physical properties such as pH, wettability, viscosity, surface tension, etc. were related to activity. 

That is, a mixture of 1-, 2-diaquo-tetrammino-cobaltic chloride and 1-, 2-diehloro-tetranimino-cobaltic chloride is formed. The aquo-salt is readily soluble in water but the diehloro-salt sparingly so. The last named forms intense blue crystals which are contaminated with small quantities of the praseo-salt, from which it may be freed by transforming it into the dithionate. The dithionate is practically insoluble, but the chloride may be regenerated from it by rubbing it with ammonium chloride. The bromide, the iodide, and the nitrate have all been prepared. 

Chlorides, bromides, and iodides can be quantitatively determined by treatment with silver nitrate, and, with suitable precautions, the precipitated halide is washed, dried, and weighed. Chlorides in neutral soln. can be determined by F. Mohr s volumetric process 27 by titration with a standard soln. of silver nitrate with a little potassium chromate or sodium phosphate as indicator. When all the chloride has reacted with the silver nitrate, any further addition of this salt gives a yellow coloration with the phosphate, and a red coloration with the chromate. In J. Volhard s volumetric process, the chloride is treated with an excess of an acidified soln. of silver nitrate of known concentration. The excess of silver nitrate is filtered from the precipitated chloride, and titrated with a standard soln. of ammonium thiocyanate, NH4CN8—a little ferric alum is used as indicator. When the silver nitrate is all converted into thiocyanate AgN03-fNH4CNS=AgCNS +NH4NOS, the blood-red coloration of ferric thiocyanate appears. 

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