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Titrations in alcohol

To conduct meaningful mechanistic and kinetic studies in alcohol media reliable and simple measurement and control of the solution jjpH is essential. Potentiometric titration is the method of choice for obtaining acid dissociation constants or metal ion complex stability constants and in favorable cases the speciation of mixtures of metal-ion-containing complexes in solution can be proposed.20 Titrations in non-aqueous solvents are not nearly as widely reported as those in aqueous media, particularly in cases with metal ions21 and determination of pH in a non-aqueous solvent referenced to that solvent is complicated due to the lack of a way to relate the electrode EMF readings to absolute jjpH (see footnote and ref. 6) so non-aqueous solvents are generally inconvenient to use22 for detailed studies of reaction mechanisms where pH control is required. [Pg.276]

The trends in IpK in passing from water to the less polar alcohols can be explained in part by considering the equilibria for carboxylic acid and aminium ion dissociation shown in Equations (4) and (5). Carboxylic acid dissociation creates two opposite charges, while aminium ion dissociation simply relocates (H+) from the amine to the solvent as ROH, which may be [Pg.277]

Acid pA), (water) jPAT, (methanol)3 jPAT, (ethanol)3 [Pg.278]


Potentiometric titrations, in alcohol, 276-278 with metal ions, 278-284 solvation effects, 277-278 Proflavine, binding with DNA, 190-194 re-systems, orthogonal, 3 in-plane and out-of-plane, 7-10... [Pg.368]

Method of Willstatter and Waldschmidt-Leitz. Direct titration in alcoholic solution with 0-1 A-alkali using phenolphthalein as indicator. [Pg.277]

Although acid-base titrations in alcohol-water mixtures have been studied extensively, we do not consider them in detail since titration curves and indicator equilibria in ethanol-water and methanol-water mixtures can be calculated in the same way as in water. Values of the autoprotolysis constants of the mixtures, are close to for mixtures containing only a moderate amount of alcohol. On the other hand, even a trace of water in ethanol causes a large increase in J SH According to Gutbezahl and Grunwald, pXsH is 14.33, 14.88, 15.91, and 19.5 for ethanol-water mixtures containing 20, 50, 80, and 100 wt % ethanol. [Pg.84]

The weaker the acid or base, the greater the extent of the hydrolysis. In the case of long-chain carboxylic acids the effect is so great that the titration cannot be done in aqueous solution, and it is necessary to use alcohol as solvent, not merely because these compounds are insoluble in water but to suppress the hydrolysis. Free alkali in soaps must be titrated in alcoholic solution any attempt to do it in aqueous solution simply results in precipitation of fatty acid, even though the solution remains alkaline. [Pg.49]

The anionic is precipitated as its p-toluidine salt, solvent-extracted, dried and weighed. It is then titrated in alcoholic solution with sodium hydroxide, which displaces the weak base. [Pg.107]

EEC titration in alkaline solution measures both species. EEC titration in acid solution measures only the sulphate or sulphonate. Potentiometric acid-base titration in alcoholic solution measures only the carboxylate. [Pg.197]

B10H14 can be titrated in aqueous/alcoholic media as a monobasic acid, pA a 2.70 ... [Pg.162]

Determination of carboxy groups. Esterification or polyesterification kinetics is usually followed by this titration which is both easy and accurate. Each sample is dissolved in a solvent or a mixture of solvents (CHCI3, QH /EtOH or MeOH, toluene/EtOH or MeOH...) and then titrated with alcoholic KOH. The end point is determined either with an indicator (in most cases phenolphthalein) or with a pH-meter. An accuracy of about 0.1-1% can generally be achieved. [Pg.56]

Turbidimetric titration has also been applied to one-phase titration of alcohol sulfates and other anionic surfactants. The titration is carried out with hyamine 1622 in aqueous solution without the organic phase and indicator and the endpoint is taken as the point of maximum turbidity. The presence of nonionics and inorganic salts at high concentration interfere with the endpoint determination [243]. [Pg.281]

Endgroup analyses were carried out with an automatic potentiometer. The [-NH2] and [-C00H] were determined simultaneously. The polymer was dissolved in o-cresol/chloroform mixture (70/30), excess alcoholic KOH added and titrated with alcoholic HCl (0.1 N). The inherent viscosities were determined in0.5% solutions... [Pg.139]

Lithium aluminium hydride Higuchi and co-workers100 introduced it as a titrant, usually in tetrahydrofuran (previously liberated from peroxide), for the titration of alcohols and phenols according to the overall reaction... [Pg.300]

The titration of metal ions in alcohol solvents28 follows the same sort of rules as titrations of metal ions in water29 but poses additional problems due to the lower polarity that increases ion pairing and oligomerization of the metal ions. We have performed several such titrations with the analysis of the potentiometric data depending on the level of information one requires. More complete and time-consuming analyses are reserved for the most effective catalytic metals, namely La3 +, and for the transition metal ion Zn2+ and Cu2+ along with some simple complexes of the latter two which we describe a little later. For the other metal ions described in our titration papers,7,8 we only present the data in terms of the... [Pg.278]

The procedure involves a titration with barium chloride and must be carried out in a 30-40% solution of alcohol in order to obtain a sharp endpoint. As the antibiotic is insoluble in alcohol it is necessary to remove the neomycin part of the molecule prior to titration. This is accomplished using a cation exchange resin such as Dowex 50-X8. [Pg.428]

The benzaldehyde should be titrated in order to determine its acidity. If it is found to contain sufficient benzoic acid to react with a considerable proportion of the sodium alcoholate,... [Pg.4]

Tributyltin carboxylates act like weak acids, and can be titrated in hexane-ethanol (1 1) medium against alkali. Tributyltin chloride (TBTC1) is also a weak acid, and gives a sharp end point when similarly titrated against sodium hydroxide. TBTCl gives an instantaneous precipitate with silver nitrate in aqueous alcoholic medium. [Pg.166]

Silver chromate is a catalyst in conversion of alcohol to aldol. It s formation signals the end point in argentometric titration in measuring halides. [Pg.839]


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Metal ion alcoholysis and titration in alcohol

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