Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Monobasic acid

The construction of the pH-logCj diagram of a monobasic acid HB is shown stepwise in Figs. 10, 11,12, 13, and 14. The acid has an overall concentration and a given pA value  [Pg.19]

Boromycin (10) will form salts with rubidium or caesium if the corresponding hydroxide is used in the hydrolytic cleavage of D-valine. The [Pg.437]


Hypophosphorous acid, H3PO2, H2P(0)0H. A monobasic acid. Ba(H2P02)2 is formed when white phosphorus is dissolved in Ba(OH)2 solution. H3PO2 and its salts are strong reducing agents. [Pg.309]

By oxidation with permanganate it forms pinonic acid, C,oH,<503, a monobasic acid derived from cyclobutane. With strong sulphuric acid it forms a mixture of limonene, dipentene, terpinolene, terpinene, camphene and p-cymene. Hydrogen chloride reacts with turpentine oil to give CioHijCl, bomyl chloride, artificial camphor . [Pg.315]

Ionisations 2, 3 and 5 are complete ionisations so that in water HCI and HNO3 are completely ionised and H2SO4 is completely ionised as a monobasic acid. Since this is so, all these acids in water really exist as the solvated proton known as the hydrogen ion, and as far as their acid properties are concerned they are the same conjugate acid species (with different conjugate bases). Such acids are termed strong acids or more correctly strong acids in water. (In ethanol as solvent, equilibria such as 1 would be the result for all the acids quoted above.) Ionisations 4 and 6 do not proceed to completion... [Pg.85]

Boron trioxide is not particularly soluble in water but it slowly dissolves to form both dioxo(HB02)(meta) and trioxo(H3B03) (ortho) boric acids. It is a dimorphous oxide and exists as either a glassy or a crystalline solid. Boron trioxide is an acidic oxide and combines with metal oxides and hydroxides to form borates, some of which have characteristic colours—a fact utilised in analysis as the "borax bead test , cf alumina p. 150. Boric acid. H3BO3. properly called trioxoboric acid, may be prepared by adding excess hydrochloric or sulphuric acid to a hot saturated solution of borax, sodium heptaoxotetraborate, Na2B407, when the only moderately soluble boric acid separates as white flaky crystals on cooling. Boric acid is a very weak monobasic acid it is, in fact, a Lewis acid since its acidity is due to an initial acceptance of a lone pair of electrons from water rather than direct proton donation as in the case of Lowry-Bronsted acids, i.e. [Pg.148]

In each case the P—O bonds have some multiple character. Phosphinic acid is a moderately strong monobasic acid. On heating the acid and its salts they disproportionate evolving phosphine ... [Pg.244]

Hydrochloric acid is a strong monobasic acid, dissolving metals to form salt and evolving hydrogen. The reaction may be slow if the chloride formed is insoluble (for example lead and silver are attacked very slowly). The rate of attack on a metal also depends on concentration thus aluminium is attacked most rapidly by 9 M hydrochloric acid, while with other metals such as zinc or iron, more dilute acid is best. [Pg.331]

Reduction of esters of monobasic acids with sodium and absolute ethyl alcohol (method of Bouveault and Blanc), for example ... [Pg.247]

By passing the vapour of a monobasic acid through a tube containing manganous oxide deposited on pumice and heated to 300-350°, the metallic ... [Pg.335]

If a mixture of monobasic acids is employed, the mixed ketone may be pre- ... [Pg.335]

SATURATED ALIPHATIC MONOBASIC ACIDS Saturated aliphatic acids may be prepared —... [Pg.354]

Place 1 0 g. of the monobasic acid and 2 g. of aniline or p-toluidine in a dry test-tube, attach a short air condenser and heat the mixture in an oil bath at 140-160° for 2 hours do not reflux too vigorously an acid that boils below this temperature range and only allow steam to escape from the top of the condenser. For a sodium salt, use the proportions of 1 g. of salt to 1 5 g. of the base. If the acid is dibasic, employ double the quantity of amine and a reaction temperature of 180-200° incidentally, the procedure is recommended for dibasic acids since the latter frequently give anhydrides with thionyl chloride. Powder the cold reaction mixture, triturate it with 20-30 ml. of 10 per cent, hydrochloric acid, and recrystallise from dilute alcohol. [Pg.362]

It is important that the solution of the sodium salt be faintly acid in order that the formation of coloured by-products in the subsequent reaction may be prevented. If the molecular weight of the monobasic acid is known, it is desirable to employ a slight excess of the sodium salt, since excess of the latter is more easily removed than the unchanged reagent. [Pg.362]

The benzene - alcohol method is useful for the esterification of valuable monobasic acids, but the b.p. of the ester must be at least 50° higher than that of benzene, for example ... [Pg.381]

This reaction is due to the combination of two da hydroxyl groups of the compound with the boric acid to form a much stronger monobasic acid ... [Pg.446]

When the corresponding monobasic acid has a trivial name, the name of the aldehyde may be formed by changing the ending -ic acid or -oic acid to -aldehyde. Examples are... [Pg.26]

Other by-products formed are relatively easy to separate, including esters of higher unsaturated monobasic acids (alkyl 3-pentenoate and 3,5-heptadienoate) (5) and esters of multiply-unsaturated dibasic acids, eg, suberates. [Pg.155]

Quality Specifications. Because of the extreme sensitivity of polyamide synthesis to impurities ia the iagredients (eg, for molecular-weight control, dye receptivity), adipic acid is one of the purest materials produced on a large scale. In addition to food-additive and polyamide specifications, other special requirements arise from the variety of other appHcations. Table 8 summarizes the more important specifications. Typical impurities iaclude monobasic acids arising from the air oxidation step ia synthesis, and lower dibasic acids and nitrogenous materials from the nitric acid oxidation step. Trace metals, water, color, and oils round out the usual specification Hsts. [Pg.246]

Monobasic acids are determined by gas chromatographic analysis of the free acids dibasic acids usually are derivatized by one of several methods prior to chromatographing (176,177). Methyl esters are prepared by treatment of the sample with BF.—methanol, H2SO4—methanol, or tetramethylammonium hydroxide. Gas chromatographic analysis of silylation products also has been used extensively. Liquid chromatographic analysis of free acids or of derivatives also has been used (178). More sophisticated hplc methods have been developed recentiy to meet the needs for trace analyses ia the environment, ia biological fluids, and other sources (179,180). Mass spectral identification of both dibasic and monobasic acids usually is done on gas chromatographicaHy resolved derivatives. [Pg.246]

Monofluorophosphoric Acid. Monofluorophosphoric acid (1) is a colorless, nonvolatile, viscous Hquid having practically no odor. On cooling it does not crystallize but sets to a rigid glass at —78°C. It has a density of = 1.818 g/mL. Little decomposition occurs up to 185°C under vacuum but it caimot be distilled. An aqueous solution shows the normal behavior of a dibasic acid the first neutralization point in 0.05 N solution is at pH 3.5 and the second at pH 8.5. Conductance measurements, however, indicate H2PO2F behaves as a monobasic acid in aqueous solution (59). The... [Pg.225]

A freshly made solution behaves as a strong monobasic acid. Neutralized solutions slowly become acidic because of hydrolysis to monofluorophosphoric acid and hydrofluoric acid. The anhydrous acid undergoes slow decomposition on distillation at atmospheric pressure, reacts with alcohols to give monofluorophosphoric acid esters, and is an alkylation (qv) and a polymerization catalyst. [Pg.226]

Polyol Esters. Polyol esters are formed by the reaction of an alcohol having two or more hydroxyl groups, eg, a polyhydric alcohol and a monobasic acid. In contrast to the diesters, the polyol in the polyol esters forms the backbone of the stmcture and the acid radicals are attached to it. The physical properties maybe varied by using different polyols or acids. Trimethylolpropane [77-99-6] C H O, and pentaerythritol [115-77-5] are... [Pg.264]

Neutralization. In water, lime ionizes readily to Ca ", Mg ", and OH , forming a strong base or alkaU. Both Ca(OH)2 and Mg(OH)2 are strong diacid bases neutralizing such strong monobasic acids as HCl and HNO, yielding neutral salts and heat. [Pg.167]

Polyol ester turbine oils currendy achieve greater than 10,000 hours of no-drain service in commercial jet aircraft with sump temperatures ranging to over 185°C. Polyol esters are made by reacting a polyhydric alcohol such as neopentyl glycol, trimethylol propane, or pentaerythritol with a monobasic acid. The prominent esters for automotive appfications are diesters of adipic and a2elaic acids, and polyol esters of trimethylolpropane and pentaerythritol (34). [Pg.245]

Nitric acid is a strong monobasic acid, a powerful oxidising agent, and nitrates many organic compounds. Until the end of the nineteenth century, it was made by heating a metallic nitrate salt with less volatile concentrated sulfuric acid. Removal of the volatile nitric acid permits the reaction to go to completion. This method is still used for laboratory preparation of the acid. [Pg.39]

Phosphinic Acid. Phosphinic acid (hypophosphoms acid) is a dehquescent crystalline soHd that melts at 26.5°C. It is a monobasic acid having a piC of 2.1 and the metal salts of which generally exhibit a high solubiUty. Phosphinic acid disproportionates upon heating above 133°C to generate phosphoric and phosphonic acids, hydrogen, and phosphine. [Pg.375]

All d Ingredients Eor each of the three principal components of alkyd reskis, the polybasic acids, the polyols, and the monobasic acids, there is a large variety to be chosen from. The selection of each of these kigredients affects the properties of the reski and may affect the choice of manufacturkig processes. Thus, to both the reski manufacturers and the users, the selection of the proper kigredients is a significant decision. [Pg.32]

Monobasic Acids. The overwhelming majority of moaobasic acids used ia alkyd resias are long-chain fatty acids of aatural occurreace. They may be used ia the form of oil or free fatty acids (see Fats and fatty oils). Free fatty acids are usually available and classified by their origin, viz, soya fatty acids, linseed fatty acids, coconut fatty acids, etc. Fats and oils commonly used ia alkyd resias are givea ia Table 4. [Pg.34]

Based on C18 fatty acids with average eq wt of 280. If the average eq wt of the monobasic acids is significantly different, adjustment is necessary. [Pg.36]


See other pages where Monobasic acid is mentioned: [Pg.21]    [Pg.173]    [Pg.265]    [Pg.247]    [Pg.275]    [Pg.366]    [Pg.427]    [Pg.780]    [Pg.645]    [Pg.241]    [Pg.268]    [Pg.123]    [Pg.31]    [Pg.31]    [Pg.35]    [Pg.421]    [Pg.430]    [Pg.63]    [Pg.113]    [Pg.114]    [Pg.386]   
See also in sourсe #XX -- [ Pg.13 ]

See also in sourсe #XX -- [ Pg.77 ]

See also in sourсe #XX -- [ Pg.166 , Pg.167 , Pg.169 ]

See also in sourсe #XX -- [ Pg.185 , Pg.186 , Pg.187 ]

See also in sourсe #XX -- [ Pg.11 ]

See also in sourсe #XX -- [ Pg.211 , Pg.213 , Pg.214 , Pg.215 ]




SEARCH



Acids, aromatic monobasic fatty

Monobasic

Monobasic Acids and Their Corresponding Bases

Monobasic acids dissociation

Monobasic acids titration

Monobasic alcohol-acids

Monobasic ketonic acids

SATURATED ALIPHATIC MONOBASIC ACIDS

Substituted aliphatic monobasic acids

© 2024 chempedia.info