Reactions of conjugated fatty acids. III. Kinetics of the Diels‐Alder reaction
- 1 June 1956
- journal article
- Published by Wiley in Journal of Oil & Fat Industries
- Vol. 33 (6) , 278-281
- https://doi.org/10.1007/bf02630861
Abstract
Summary: The kinetics of a Diels‐Alder‐type reaction between diethylazodicarboxylate andt,t‐9,11‐octadecadienoic acid has been studied in various solvent systems and with acidic catalysts. The rate of the reaction was found to vary as follows: a) the reaction rate is faster in polar solvents than in nonpolar solvents; b) addition of acidic catalysts to nonpolar solvents increases the rate of the reaction, and acidic catalysts appear to have no effect on the rate of reaction in polar solvents; c) when compatibility can be maintained, addition of water to polar solvent systems appears to increase the reaction rate in proportion to the amount of water added.The reaction follows second‐order or pseudo second‐order kinetics. Probably it is more complex than the over‐all reaction kinetics indicate. Certain reactions were studied at two temperatures, and information on activation energy of the reaction has been obtained.Keywords
This publication has 3 references indexed in Scilit:
- Isomers of Conjugated Fatty Acids. I. Alkali-isomerized Linoleic AcidJournal of the American Chemical Society, 1951
- Pseudo-eleostearic AcidJournal of the American Chemical Society, 1939
- Einige Beiträge zur Kenntniss der Ricinusöl-, Ricinelaïdin- und RicinstearolsäureMonatshefte für Chemie / Chemical Monthly, 1894