Hydration of Alkenes With Aqueous Acid
Hydration of Alkenes to Give Alcohols When alkenes are treated with aqueous acid (H3O+) they can be converted to alcohols. Formation of the new C-OH
Read moreHydration of Alkenes to Give Alcohols When alkenes are treated with aqueous acid (H3O+) they can be converted to alcohols. Formation of the new C-OH
Read moreBromination, Chlorination, and Halohydrin Formation from Alkenes Alkenes undergo halogenation when treated with Cl2, Br2 and (less commonly) I2 to give vicinal dihalides These reactions
Read morem-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
Read moreOsmium 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
Read moreCatalytic 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
Read moreCyclopropanation 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
Read moreThe “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
Read moreElimination Reactions: The Zaitsev Rule Elimination reactions usually occur such that they are removing a hydrogen from the carbon attached to the fewest hydrogens. This
Read moreThe E1 Reaction – Three Key Pieces of Evidence, and a Mechanism Last time in this walkthrough on elimination reactions, we talked about two types
Read moreElimination Reactions Using “Bulky Bases” – When The Zaitsev Product Is Minor We’ve recently talked about Zaitsev’s rule in elimination reactions, and how the transition
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