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Polyfunctional acids

More recendy, so-called overbased driers with even higher metal contents have become available. These driers are made with combinations of monocarboxyhc acids and carbon dioxide or polyfunctional acids. [Pg.217]

We can generalize that it is going to be more difficult to lose a proton from an anion than from an uncharged molecule. This is also true of polyfunctional acids, such as dicarboxylic acids. However, it is found that this effect diminishes as the negative centres become more separated. Thus, pATa values for some simple aliphatic dicarboxylic acids are as shown, loss of the first proton being represented by pATai and loss of the second by pATa2-... [Pg.144]

The leaving groups most commonly employed in nature are phosphates and diphosphates. These good leaving groups are anions of the strong acids phosphoric (pATa 2.1) and diphosphoric (pATa 1.5) acids respectively. The p a values given refer to the first ionization of these polyfunctional acids (see Section 4.7). [Pg.196]

Alkyd. Alkyd resins are the reaction product of a poly functional alcohol and a polyfunctional acid. When the resin is combined with a filler, catalyst, pigment, and release agent the resultant product is a granular or putty or rope-type molding compound. Fillers used may be fine mineral, glass, mineral and nylon—depending on the end product desired. [Pg.29]

NMR longitudinal relaxation times can be used for determination of the site of protonation in polyfunctional acids and bases (93JCS(P2)283). Thus, the 14N NMR spectrum of 4-aminopyridine shows clearly from the sharpening of the signal for the ring nitrogen that protonation has occurred here. This procedure is an important innovation in the elucidation of heterocyclic tautomeric structures, especially for the cases of fast exchange. [Pg.34]

Polyfunctional acids and bases play important roles in many chemical and biological systems. The human body contains a complicated system of buffers within cells and within bodily fluids, such as human blood. The photo is a scanning electronmicro-... [Pg.395]

This chapter describes polyfunctional acid and base systems, including buffer solutions. Calculations of pH and titration curves are also described. [Pg.395]

Phosphoric acid is a typical polyfunctional acid. In aqueous solution, it undergoes the following three dissociation reactions ... [Pg.399]

Thus far, we have not considered how to calculate the pH of solutions of salts that have both acidic and basic properties—that is, salts that are amphiprotic. Such salts are formed during neutralization titration of polyfunctional acids and bases. For example, when 1 mol of NaOH is added to a solution containing 1 mol of the acid... [Pg.403]

Spreadsheet Summary In Chapter 8 of Applications of Microsoft Excel in Analytical Cheniistiy, we extend the treatment of neutralization titration curves to polyfunctional acids. Both a stoichiometric approach and a master equation approach are used for the titration of maleic acid with sodium hydroxide. [Pg.416]

Note that these expressions are analogous to the a expressions we wrote for polyfunctional acids and bases except that the equations here are written in terms of formation equilibria while those for acids or bases are written in terms of dissociation equilibria. Also, the master variable is the ligand concentration [L] instead of the hydronium ion concentration. The denominators are the same for each a value. Plots of the a values versus p[L] are known as distribution diagrams. [Pg.452]

The alpha values for metal-ligand complexes can be derived in the same way that we derived values for polyfunctional acids in Section 15H. The alphas are... [Pg.452]

Polyfunctional acids and bases Species that contain more than... [Pg.1115]

Chapter 8 Polyfunctional Acids and Bases Chapter 15 Poly functional Acids and Bases Chapter 13 Polyfunctional Acids and Bases... [Pg.1176]

POLYMERIZATION OF ALLYL ESTERS OF OTHER POLYFUNCTIONAL ACIDS... [Pg.322]

Many esters of polyfunctional acids have been prepared. For example, triallyl citrate was mentioned in Chia and Chao [108]. Simpson and Holt [41,42] studied the oxalate and sebacate. Matsumoto and Oiwa [46,47] worked with the carbonate, oxalate, malonate, succinate, adipate, and sebacate. Early works with... [Pg.322]

Polymerization of AUyl Esters of Other Polyfunctional Acids... [Pg.323]

Some polyfunctional acidic compounds remain In the acidified water phase D. An alternate route using Ion exchange resin Is better suited for separation and identification of polyfunctional acidic compounds, such as hydroxybenzolc acid. These compounds will end up in the water extract labeled E in Figure 1. Unless other soluble compounds mask their presence, these acids can also be Identified in the original extracted fermentation broth. [Pg.269]

Na-a-naphthylacetate stirred 5-10 min. at room temp, with phosphonitrile chloride in tetrahydrofuran, a 6-10-fold excess of cyclohexylamine added, and stirring continued 5-10 min. -> N-cyclohexyl-a-naphthylacetamide. Y 82%. - A variety of solvents may be used for this simple and mild reaction, which gives high yields even with polyfunctional acids. F. e., also from the acids with and without triethylamine, and hydrazides s. L. Caglioti, M. Poloni, and G. Rosini, J. Org. Chem. 33, 2979 (1968). [Pg.377]

The treatment of polyfunctional acids by alcohols in the presence of strong inorganic acids as catalysts can simultaneously be accompanied by the derivatization of other functional groups. For example, carbonyl groups in keto-carboxylic acids are converted into dialkylketal fragments in the presence of in ketocarboxylic acids. [Pg.5]

Compatibility Corrosion inhibitors can undergo reactions with components of the environment. Amines react with HjS. Unsaturated fatty acids and derivatives thereof (imidazolines) are subject to vulcanization in the presence of elemental sulfur or oxygen in combination with HjS. Polyfunctional acids react with polyfunctional amines to form gels or solids. Such considerations are important, since production or process streams are often treated with more than one chemical (oil and gas production processing, transport and refining, cooling water circuits— the examples are endless). [Pg.481]

By incorporation of polyfunctional acid anhydrides a network structure may also be built whilst it is also possible to build up sites for cross-linking. [Pg.365]


See other pages where Polyfunctional acids is mentioned: [Pg.290]    [Pg.215]    [Pg.144]    [Pg.145]    [Pg.187]    [Pg.66]    [Pg.269]    [Pg.40]    [Pg.41]    [Pg.399]    [Pg.399]    [Pg.407]    [Pg.407]    [Pg.409]    [Pg.413]    [Pg.415]    [Pg.424]    [Pg.179]    [Pg.89]   
See also in sourсe #XX -- [ Pg.55 , Pg.91 , Pg.93 ]




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