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  2. Alkyne - Wikipedia

    en.wikipedia.org/wiki/Alkyne

    In the language of valence bond theory, the carbon atoms in an alkyne bond are sp hybridized: they each have two unhybridized p orbitals and two sp hybrid orbitals. Overlap of an sp orbital from each atom forms one sp–sp sigma bond. Each p orbital on one atom overlaps one on the other atom, forming two pi bonds, giving a total of three bonds.

  3. Frontier molecular orbital theory - Wikipedia

    en.wikipedia.org/wiki/Frontier_molecular_orbital...

    Theory. Fukui realized that a good approximation for reactivity could be found by looking at the frontier orbitals (HOMO/LUMO). This was based on three main observations of molecular orbital theory as two molecules interact: The occupied orbitals of different molecules repel each other. Positive charges of one molecule attract the negative ...

  4. Azide-alkyne Huisgen cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Azide-alkyne_Huisgen_cyclo...

    The azide-alkyne Huisgen cycloaddition is a 1,3-dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3-triazole. Rolf Huisgen [1] was the first to understand the scope of this organic reaction. American chemist Karl Barry Sharpless has referred to copper-catalyzed version of this cycloaddition as "the cream of ...

  5. Dewar–Chatt–Duncanson model - Wikipedia

    en.wikipedia.org/wiki/Dewar–Chatt–Duncanson...

    On the right, an empty pi-antibonding orbital on C 2 H 4 overlaps with a filled d-orbital on the metal. The Dewar–Chatt–Duncanson model is a model in organometallic chemistry that explains the chemical bonding in transition metal alkene complexes. The model is named after Michael J. S. Dewar, [1] Joseph Chatt and L. A. Duncanson. [2][3]

  6. Bürgi–Dunitz angle - Wikipedia

    en.wikipedia.org/wiki/Bürgi–Dunitz_angle

    In the addition of a nucleophile (Nu) attack to a carbonyl, the BD angle is defined as the Nu-C-O bond angle. The BD angle adopted during an approach by a nucleophile to a trigonal unsaturated electrophile depends primarily on the molecular orbital (MO) shapes and occupancies of the unsaturated carbon center (e.g., carbonyl center), and only secondarily on the molecular orbitals of the ...

  7. Zaytsev's rule - Wikipedia

    en.wikipedia.org/wiki/Zaytsev's_rule

    Zaytsev's rule. In organic chemistry, Zaytsev's rule (or Zaitsev's rule, Saytzeff's rule, Saytzev's rule) is an empirical rule for predicting the favored alkene product (s) in elimination reactions. While at the University of Kazan, Russian chemist Alexander Zaytsev studied a variety of different elimination reactions and observed a general ...

  8. Transition metal alkene complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_alkene...

    Transition metal alkene complex. In organometallic chemistry, a transition metal alkene complex is a coordination compound containing one or more alkene ligands. The inventory is large. [1] Such compounds are intermediates in many catalytic reactions that convert alkenes to other organic products. [2]

  9. Nitrone-olefin (3+2) cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Nitrone-olefin_(3+2...

    Nitrone-olefin (3+2) cycloaddition. The nitrone-olefin (3+2) cycloaddition reaction is the combination of a nitrone with an alkene or alkyne to generate an isoxazoline or isoxazolidine via a (3+2) cycloaddition process. [1] This reaction is a 1,3-dipolar cycloaddition, in which the nitrone acts as the 1,3-dipole, and the alkene or alkyne as the ...