Browsing by Subject "Elimination reactions"
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Item A mechanistic study of complex base-promoted 1,2-elimination reactions(Texas Tech University, 1983-12) Croft, Alan PaulNot availableItem Carbon-nitrogen double bond-forming elimination reactions involving 2-alkyl- and 2-arylpyrrolidines(Texas Tech University, 1980-05) Yilmaz, IbrahimNot availableItem Elimination reactions forming carbon-nitrogen double bonds(Texas Tech University, 1980-05) Cho, Bong-raeNot availableItem Orientation in vinyl activated 1,2-elimination reactions(Texas Tech University, 1979-05) Haines, Jeffrey CharlesNot availableItem Stereochemistry of base promoted β-elimination from dihalocycloalkanes and 2-monosubstituted norbornanes(Texas Tech University, 1978-12) Lee, Jong GunElimination reactions are one of the four fundamental classes of reactions of organic compounds. The most frequently encountered type of elimination is β-elimination which involves the heterolytic cleavage of two bonds and the formation of a new multiple bond linkage. This process can be accomplished by a variety of mechanistic possibilities ranging from multistep reactions to concerted processes with different electron distributions and geometries. Three basic mechanisms of 3-elimination reactions have been recognized. These mechanisms differ chiefly in the timing of the carbonhydrogen and carbon-leaving group cleavage and are termed El, ElcB, and E2 mechanism.