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Electrocyclic reactions - thermal

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Apr 14, 2018
11:37

Tutorials, practice problems and more at https://organicchemexplained.com By looking at the HOMO of a substrate undergoing electrocyclic reaction, and taking symmetry constraints into account, the stereochemical outcome of the thermal reaction, ie. with heating, can be predicted. The example is a 1,3,5-hexatriene undergoing thermal electrocyclization via a disrotatory process. Organic Chemistry Explained!: https://organicchemexplained.com Twitter: https://twitter.com/MarkCoster_Chem LinkedIn: https://www.linkedin.com/in/markjcoster/ Academic website: https://mcoster.net

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