Diels-Alder Reactions | 16.5 Organic Chemistry

Chad provides a comprehensive lesson on Diels-Alder reactions, a concerted 4 + 2 cycloaddition reaction. He covers the reaction mechanism and shows how to predict the relative reactivities of dienes and dienophiles. He then describes and demonstrates both the stereoselectivity and regioselectivity observed in Diels-Alder reactions. Chad then shows examples of how Diels-Alder reactions with cyclic dienes result in bicyclic compounds and how the Endo Rule describes the stereoselectivity in such examples. Finally, Chad covers the conservation of orbital symmetry, showing how the symmetry of the HOMO of the diene and the LUMO of the dienophile match which makes Diels-Alder reactions symmetry allowed. 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-organ... If you want all my study guides, quizzes, and practice exams, check out my premium course at https://school.chadsprep.com/subscrip... 00:00 Lesson Introduction 00:43 Introduction to Pericyclic Reactions 02:18 Introduction to Diels-Alder Reactions 04:50 Relative Reactivities of Dienes 11:29 Relative Reactivities of Dienophiles 13:04 Stereoselectivity in Diels-Alder Reactions 19:06 Regioselectivity in Diels-Alder Reactions 29:19 Diels-Alder Reactions with Cyclic Dienes 41:24 Conservation of Orbital Symmetry https://www.chadsprep.com/ #organicchemistry #organicchemistrytutorial #dielsalder