16.7 Electrocyclic Reactions | Organic Chemistry

Chad provides a comprehensive lesson on Electrocyclic Reactions, ring-openings and ring closures. He begins by comparing thermal and photochemical conditions for a ring closure. He then shows how disrotatory or conrotatory rotation in the transition state needs to lead to constructive overlap for a reaction to be 'allowed.' He then summarizes the Woodward-Hoffmann rules as they pertain in electrocyclic reactions. Chad concludes the lesson by showing how to predict the stereochemistry of the products of electrocyclic reactions. I've created an organic chemistry page that organizes all my videos by chapter - just an easier way for you to watch my YouTube videos. Check it out at https://www.chadsprep.com/chads-organic-chemistry-videos/ Do you want Chad’s Organic Chemistry Study Guides and Practice Quizzes/Tests? Check out Chad’s Organic Chemistry Master Course. Free Trial available! https://www.chadsprep.com/organic-chemistry-free-trial/ https://www.seevid.ir/fa/w/u3jbkE4lWAE Lesson Introduction https://www.seevid.ir/fa/w/u3jbkE4lWAE Electrocyclic Reactions; Thermal vs Photochemical Conditions https://www.seevid.ir/fa/w/u3jbkE4lWAE Disrotatory vs Conrotatory https://www.seevid.ir/fa/w/u3jbkE4lWAE Summary of Woodward-Hoffmann Rules https://www.seevid.ir/fa/w/u3jbkE4lWAE Predicting Stereochemistry in Electrocyclic Reactions https://www.chadsprep.com/

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