Carboxylic acids, equivalent weights reactions

The neutralization equivalent is a useful means of determining the molecular weight of a carboxylic acid. The process begins with a simple neutralization reaction of acid with standard base (usually sodium hydroxide). The reaction is... 

Chain Extension of -U-Polystyrene Hiols. A two-stage chain extension of the. -kJ -polystyrene diols was accomplished by carboxylation of the diols with succinic anhydride followed by chain extension with a diepoxide. The succinic anhydride reaction was carried out 120-130°C under nitrogen. The reaction was monitored bj changes in the carbonyl bands at 1715 and 1740 cm in the infrared spectra of the reaction mixtures. The resulting dicarboxylic acid polymers were chain-extended in bulk at 130°C for 9 hours with Sow s HER diepoxide, equivalent weight =171, using bis( 3,5-diisopropylsalicylato)Cr (III) as the catalyst. 

Carboxylic acids, esters, amides, nitriles, nitro groups and most aromatic nuclei are not reduced under ionic hydrogenation conditions (133). An organosiloxane, polymethylhydrosiloxane [9004-73-3] (PMHS), is most economically favored for large-scale reductions. Polymethylhydrosiloxane is a versatile low cost hydride transfer reagent having a hydride equivalent weight of 60. Reactions are catalyzed by Pd or dibutyltinoxide. The choice of reaction conditions leads to chemoselective reduction, eg, allyl reductions in the presence of ketones and aldehydes (134—136). Esters are reduced to... 

The amount of elastomer contained in a rubber-modified epoxy resin is usually dictated by the final application and material properties desired. Knowing that one equivalent of epoxide reacts with one equivalent of carboxylic acid and the final concentration of elastomer that is desired, one can add another term to Equation (2) to account for the equivalents of epoxide consumed during the esterification reaction. The equivalent weight of the CTBN elastomers vary from lot to lot but is typically —1800 g eq . Using this number as an example, the expanded equation now reads,... 

If the dicarboxylic acid has been present in excess in the reaction mixture, then the resulting polyester uses up more sodium hydroxide for the same Molecular weight of the polyester which has been prepared by the complete equivalencies of the monomers. If the amount of dicarboxylic acid during the synthesis of the ester is very high and if all the molecules of the polymers contain carboxyl groups at both ends, then the consumption of sodium Organisation and Qualities... 

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