8: Substitution Reactions of Alkyl Halides Last updated Jun 23, 2019 Save as PDF 7.12: The Diels-Adler Reaction Is a 1,4-Addition Reaction 8.1: The Mechanism For an SN2 Reaction Page ID13890 ( \newcommand{\kernel}{\mathrm{null}\,}\) An Introductory Organic Chemistry Textmap organized around Paula Bruice's textbook Organic Chemistry I II III IV V VI VII VIII IX X XI XII XIII XIV XV XVI XVII XVIII XIX XX XXI XXII XXIII XXIV XXV XXVI XXVII XXVIII XXIX XXX XXXI Template:HideTOC Topic hierarchy8.1: The Mechanism For an SN2 Reaction8.2: Factors That Affect SN2 Reactions8.3: The Reversibility of an SN2 Reaction Depends on the Basicities of the Leaving Groups in the Forward and Reverse Directions8.4: The Mechanism for an SN1 Reaction8.5: Factors That Affect SN1 Reactions8.6: More About the Stereochemistry of SN2 and SN1 Reactions8.7: Benzylic Halides, Allylic Halides, Vinylic Halides, and Aryl Halides8.8: Competition Between SN2 and SN1 Reactions8.9: The Role of the Solvent in SN2 and SN1 Reactions8.10: Intermolecular Versus Intramolecular Reactions8.11: Biological Methylating Reagents Have Good Leaving Groups