Bases acidifiable

Tar Bases.—Acidify 1 gm. of ammonium carbonate with 5 cc. of nitric acid, and evaporate the solution to dryness on the water-bath. The residue must have a pure white color. 

These three examples illustrate technology developments over time (dual-channel detector, diode array detector, mass spectrometer). Note that while the overall methodology is very similar (methanolic extracts, methanol-based, acidified solvents used for HPLC, detection of eluted compounds), the exact conditions for successful separation need to be defined for each system. 

Table 1. Phosphoric acid-based acidifier for weaned piglets (0-13 days post weaning) (Schoenherr,...

Schoenherr, W.D. (1994) Phosphoric acid-based acidifiers explored for starter diets. Feedstuffs 66 40. 

In 1785 de Morveau said Lavoisier had supposed that sugar when treated with nitric acid becomes acid of sugar acide saccharin) (oxalic acid) by taking up vital air, as sulphur forms vitriolic acid and phosphorus phosphoric acid (see p. 424). But if sugar enters undecomposed into acid of sugar it must exist in all other substances from which this acid is extracted by the same means, which cannot be accepted. The acid is really formed by the combination of vital air with a particular radical (radical particulier ou base acidifiable) found in numerous bodies of different kinds, in this case the radical saccharin. Thus de Morveau introduced the name radical into organic chemistry. 

METHOD 2 [89]--1M MDA or benzedrine and 1M benzaldehyde is dissolved in 95% ethanol (Everclear), stirred, the solvent removed by distillation then the oil vacuum distilled to give 95% yellow oil which is a Schiff base intermediate. 1M of this intermediate, plus 1M iodomethane, is sealed in a pipe bomb that s dumped in boiling water for 5 hours giving an orangy-red heavy oil. The oil is taken up in methanol, 1/8 its volume of dH20 is added and the solution refluxed for 30 minutes. Next, an equal volume of water is added and the whole solution boiled openly until no more odor of benzaldehyde is detected (smells like almond extract). The solution is acidified with acetic acid, washed with ether (discard ether), the MDMA or meth freebase liberated with NaOH and extracted with ether to afford a yield of 90% for meth and 65% for MDMA. That s not a bad conversion but what s with having to use benzaldehyde (a List chemical) Strike wonders if another aldehyde can substitute. 

A regioselective aldol condensation described by Biichi succeeds for sterical reasons (G. Biichi, 1968). If one treats the diaidehyde given below with acid, both possible enols are probably formed in a reversible reaaion. Only compound A, however, is found as a product, since in B the interaction between the enol and ester groups which are in the same plane hinders the cyclization. BOchi used acid catalysis instead of the usual base catalysis. This is often advisable, when sterical hindrance may be important. It works, because the addition of a proton or a Lewis acid to a carbonyl oxygen acidifies the neighbouring CH-bonds. 

Analytical Procedures. Oxygen difluoride may be determined conveniently by quantitative appHcation of k, nmr, and mass spectroscopy. Purity may also be assessed by vapor pressure measurements. Wet-chemical analyses can be conducted either by digestion with excess NaOH, followed by measurement of the excess base (2) and the fluoride ion (48,49), or by reaction with acidified KI solution, followed by measurement of the Hberated I2 (4). 

Sulfates. Indium metal and its oxides dissolve in warm sulfuric acid to give a solution of the trisulfate [13464-82-9], In2(S0 2- It is a white, crystalline, deUquescent soHd, readily soluble in water that forms double salts with alkaLi sulfates and some organic substituted ammonium bases. Concentration of the acidified trisulfate solution produces indium acid sulfate crystal [57344-73-7], In(HS0 2> other reaction conditions give basic sulfates. 

Uranium ores are leached with dilute sulfuric acid or an alkaline carbonate [3812-32-6] solution. Hexavalent uranium forms anionic complexes, such as uranyl sulfate [56959-61-6], U02(S0 3, which are more selectively adsorbed by strong base anion exchangers than are other anions in the leach Hquors. Sulfate complexes are eluted with an acidified NaCl or ammonium nitrate [6484-52-2], NH NO, solution. Carbonate complexes are eluted with a neutral brine solution. Uranium is precipitated from the eluent and shipped to other locations for enrichment. Columnar recovery systems were popular in South Africa and Canada. Continuous resin-in-pulp (RIP) systems gained popularity in the United States since they eliminated a difficult and cosdy ore particle/leach hquor separation step. 

A process based on saponification of ethylene—acrylate ester copolymers has been practiced commercially in Japan (29). The saponification naturally produces fully neutralized polymer, and it is then necessary to acidify in order to obtain a pardy neutralized, melt-processible product. Technology is described to convert the sodium ionomer produced by this process to the zinc type by soaking pellets in zinc acetate solution, followed by drying (29). 

Analytical Methods. Analysis of fresh and spent peroxides and superoxides is done by adding the material to water. Approximately 0.1 wt % permanganate is used in the water to decompose the peroxide ion which otherwise forms. The evolved oxygen is measured volumetricaHy. If the material is spent, the base strength is titrated to a phenolphthalein end point, acidified further, and the carbon dioxide is deterrnined volumetricaHy. 

Benzene SuIfona.tion. In the benzene sulfonation process, benzene reacts with concentrated sulfuric acid to form benzenesulfonic acid at about 150°C. The benzenesulfonic acid is neutralized with sodium sulfate to produce sodium benzenesulfonate, which is then fused with caustic soda to yield sodium phenate. The sodium phenate is acidified with sulfur dioxide and a small amount of sulfuric acid to release the phenol from the sodium salt. The phenol yield by this process can be as high as 88 mol % to that of the theoretical value based on benzene. Plants employing this technology have been shut down for environmental and economic reasons. 

The DAG conversion to L-ascorbic acid also can occur by a base-catalyzed mechanism. Methyl 2-oxo-L-gulonate (methyl DAG) is converted, on treatment with sodium methoxide, to sodium-L-ascorbate, which is then acidified to L-ascorbic acid. Various solvent systems have been evaluated and reported (46). 

Two colorimetric methods are recommended for boron analysis. One is the curcumin method, where the sample is acidified and evaporated after addition of curcumin reagent. A red product called rosocyanine remains it is dissolved in 95 wt % ethanol and measured photometrically. Nitrate concentrations >20 mg/L interfere with this method. Another colorimetric method is based upon the reaction between boron and carminic acid in concentrated sulfuric acid to form a bluish-red or blue product. Boron concentrations can also be deterrnined by atomic absorption spectroscopy with a nitrous oxide—acetjiene flame or graphite furnace. Atomic emission with an argon plasma source can also be used for boron measurement. 

Chlorous Acid. The physical properties of HCIO2 have been determined using acidified alkah metal chlorite solutions. The existence of HCIO2 is based on spectroscopic evidence (6,13,97). 

This is the final neutralizing rinse after the pre-treatment to obtain a better corrosion resistance. The phosphated surfaces are treated with chromic acid-based or acidified sodium dichromate solutions which are not affected by moisture and thus protect the phosphate coating. 

Hydrogen cyanide, mp —13.3° bp 25.7°, is an extremely poisonous compound of very high dielectric constant (p. 55). It is miscible with H2O, EtOH and Et20. In aqueous solution it is an even weaker acid than HE, the dissociation constant Ka being 7.2 x 10 ° at 25°C. It was formerly produced industrially by acidifying NaCN or Ca(CN)2 but the most modem catalytic processes are based on direct reaction between... 

The free base was then dissoived in absolute methanol, and the resulting solution was then adjusted to an acid pH value with an ethereal hydrochloric acid solution. The acidified solution was purified with charcoal and then dry ether was added thereto until crystallization took place. The hydrochloride, prepared in this customary manner, had a melting point of 305°C according to U.S. Patent 3,202,660. 

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