Acids and Their Salts

Although a number of acids containing arsenic, antimony, and bismuth are known, they are of little importance compared to the acids containing phosphorus. Also, the acid of bismuth, H3Bi03, can also be written as Bi(OH)3, and in keeping with the metallic character of bismuth it is not actually very acidic. Because of their great importance, the discussion that follows is concerned with the acids containing phosphorus. 

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All the halic(V) acids are strong acids and their salts are not appreciably hydrolysed in aqueous solution. They are also powerful oxidising agents (see below). 

Thiazole acetic acids and their hotnologs can also be prepared by cyclization procedures 4-thiazole alkanoic acids and their salts were prepared by treating a thioamide with a -y-chloro- or 7-bromoacetoacetic or their a-alkyl derivatives (4, 10, 16, 22, 273, 275, 281, 640, 647, 695). 

Similarly, 5-thiazole alkanoic acids and their salts are obtained from thioamides and /3-halo -y-keto acids (695). Thus thioarylamides condensed with 3-aroyl-3-bromopropionic acid (88) in isopropanolic solution in the presence of Na COs give first 4-hydroxy-2-aryl-A-2-thiazoline-5-acetic acid intermediates (89), which were dehydrated in toluene with catalytic amounts of p-toluene sulfonic acid to 2,4-diaryl-5-thiazole acetic acid (90) (Scheme 39) (657), with R = H or Me Ar = Ph, o-, m- or p-tolyl, o-, m-, or P-CIC6H4, 0-, m-, or p-MeOC(iH4, P-CF3C6H4, a-thienyl, a-naphthyl (657). 

Peroxophosphoric Acids and Their Salts. In its usual impure form (H PO is the main contaminant), peroxomonophosphoric acid [13598-52-2] (5), is a viscous, coloress Hquid. The three ionization constants for peroxomonophosphoric acid are pifj = 1.1, P-A2 = 5.5, and pK (peroxide proton) = 12.8 (44). Oxidations comparable to those of peroxomonosulfuric acid, H2SO, occur in acid solutions of ca pH 2, but at higher pH values, H PO becomes less reactive as an oxidant and more unstable with respect to decomposition (44). The stmcture of H PO is probably similar to that of... 

Peroxosulfiiric Acids and Their Salts. Two kiads of peroxosulfiiric acid are known peroxomonosulfuric and peroxodisulfuric acids. Neither is available commercially ia the pure state. The name Caro s acid is commonly used as a synonym for peroxomonosulfuric acid, but is better reserved for the equiUbrium mixture with sulfuric acid. 

Organoperoxysulfonic acids and their salts have been prepared by the reaction of arenesulfonyl chlorides with calcium, silver, or sodium peroxide treatment of metal salts of organosulfonic acids with hydrogen peroxide hydrolysis of di(organosulfonyl) peroxides, RS(0)2—OO—S(02)R, with hydrogen peroxide and sulfoxidation of saturated, non aromatic hydrocarbons, eg, cyclohexane (44,181). 

EDA reacts with formaldehyde and sodium cyanide under the appropriate alkaline conditions to yield the tetrasodium salt of ethylenediaminetetraacetic acid (24). By-product ammonia is removed at elevated temperatures under a partial vacuum. The free acid or its mono-, di-, or trisodium salts can be produced by the appropriate neutrali2ation using a strong mineral acid. This same reaction with other amines is used to produce polyamino acetic acids and their salts. These products are used widely as chelating agents. 

Polypropylene Polypropylene (PP) pipe and fittings have excellent resistance to most common organic and mineral acids and their salts, strong and weak alkahes, and many organic chemicals. They are available in sizes V2 through 6 in, in Schedules 40 and 80, but are not covered as such by ASTM specifications. 

Other direct methods for the sulfonation of the higher fatty acids are by the use of sulfur trioxide vapor or by the use of chlorosulfonic acid. Indirect methods are also available for the preparation of a-sulfo fatty acids and their salts from an a-bromo fatty acid made by the Hell-Volhard-Zelinsky reaction. The bromo compound may be converted directly to the sodium salt of a sulfonic acid through the Strecker reaction or may be converted to the mercaptan and oxidized to the sulfonate. Sulfonation of the lower fatty acids has been studied by Backer and co-workers. ... 

Perch ramie and Per poly perchromic Acids and Their Salts... 

Selenium is stable in water and in aqueous solutions over the entire pH interval in the absence of any oxidizing or reducing agent. Selenium can be electrochemically reduced to hydrogen selenide or to selenides that are unstable in water and aqueous solutions. It can be oxidized to selenous acid or selenites and further (electrolyti-cally) to perselenic acid (H2Se20s). Selenic and selenous acids and their salts are stable in water. The selenides, selenites, and selenates of metals other than the alkali metals are generally insoluble. 

Chowhan, Z. T. pH-solubility profiles of organic carboxylic acids and their salts. 

Bisphosphonic acids and their salts are analogs of pyrophosphate where the P-O-P linkage of the latter has been replaced by P-C-P. Bisphosphonates are known to inhibit bone resorption, and have attracted much attention as potential therapeutic agents. Bisphosphonates do not absorb or fluoresce, and sample matrix interferences can make detection difficult, especially in biological samples. Successful applications of IEC to bisphosphonate analysis have been described.173174... 

A general equation for the chlorination of certain dithiophosphoric acids and their salts can be written as follows ... 

Chowhan, Z. T., pH-solubility profiles of organic carboxylic acids and their salts, J. Pharm. Sci. 67, 1257-1260 (1978). 

M. Faraday was the first to observe an electrocatalytic process, in 1834, when he discovered that a new compound, ethane, is formed in the electrolysis of alkali metal acetates (this is probably the first example of electrochemical synthesis). This process was later named the Kolbe reaction, as Kolbe discovered in 1849 that this is a general phenomenon for fatty acids (except for formic acid) and their salts at higher concentrations. If these electrolytes are electrolysed with a platinum or irridium anode, oxygen evolution ceases in the potential interval between +2.1 and +2.2 V and a hydrocarbon is formed according to the equation... 

Around 10-40% of the chemical consumption in a tannery is organic chemicals. Examples of standard organic chemicals used are organic acids and their salts. 

For A1 in organic electrolytes (for instance, aliphatic acids and their salts) and in inorganic electrolytes which form porous oxide films (e.g., sulfuric acid), a broad and rather intense emission maximum is found,313,314 whose origin is probably connected with incorporated anions. 

G. F. Smith, Analytical Applications of Periodic Acid and Iodic Acid and Their Salts, G. Frederick Smith Chemical Co., Columbus, Ohio, 5th Edition, 1950, p. 7 (Manufacturer s circular). 

Numerous preparative methods have been reported for these acids and their salts and ester derivatives.1 4 Dithiophosphoric acids are accessible from the reaction of phosphorus pentasulfide with alcohols or phenols (Equation 18). Dithiophosphinic acids can be prepared from thiophosphinic chlorides and sodium hydrosulfide (Equation 19), although the phenyl derivative is better prepared using a modified Friedel-Crafts reaction in which phosphorus pentasulfide is reacted with benzene in the presence of anhydrous aluminium trichloride (Equation 20). 

Buffers contain mixtures of weak acids and their salts (i.e., the conjugate bases of acids), or mixtures of weak bases and their conjugate acids. Typical buffer systems used in pharmaceutical dosage forms include mixtures of boric acid and sodium borate, acetic acid and sodium acetate, and sodium acid phosphate and disodium phosphate. The reason for the buffering action of a weak acid, HA (e.g., acetic acid) and its ionized salt, A" (e.g., sodium acetate) is that A" ions from the salt combine with the added hydrogen ions, removing them from solution as undissociated weak acid. 

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