The Mechanism For Hydrohalogenation of Alkenes, Acid-Catalyzed Hydration of Alkenes, and Acid-Catalyzed Addition of Alcohols To Alkenes: The Carbocation Pathway In Alkene Addition Reaction Mechanisms
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Recall that there are at least 4 major ways of representing molecules that you’re introduced to in the first week of ochem. The highest level
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Hydroboration Oxidation of Alkenes In this article we cover one of the most important methods for forming alcohols from alkenes, hydroboration-oxidation. Hydroboration is an addition reaction between an alkene
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m-Chloroperoxybenzoic Acid (m-CPBA) For The Epoxidation of Alkenes m-CPBA (meta-chloroperoxybenzoic acid) is a useful reagent for the formation of epoxides from alkenes (note – often
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Osmium tetroxide, OsO4 Osmium tetroxide (OsO4) is a useful reagent for the dihydroxylation of alkenes The products of these reactions are 1,2-diols (“vicinal” diols), where the two
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Catalytic Hydrogenation of Alkenes With Pd/C (And Friends) Alkenes (and alkynes) will undergo addition of hydrogen (H2) in the presence of a metal catalyst such
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Today, in partnership with Rich Apodaca of Metamolecular, I’m happy to announce the release of a new app for the Apple iOs: Organic Reaction Flashcards
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Loyal reader “Nathan” (not his real name) sent in this note recently on how he managed to do well in organic chemistry without it having
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Cyclopropanation of Alkenes Alkenes can undergo addition reactions from carbenes to give cyclopropanes. There are three main pathways for this reaction that are generally covered in introductory
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The “Three-Membered Ring” Pathway In Alkene Mechanisms: Halogenation, Oxymercuration, Halohydrin Formation, and Acidic Epoxide Opening In the last post we walked through a proposal for
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