enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Pericyclic reaction - Wikipedia

    en.wikipedia.org/wiki/Pericyclic_reaction

    Example of a pericycle reaction: the norcaradiene–cyclohexatriene rearrangement. In organic chemistry, a pericyclic reaction is the type of organic reaction wherein the transition state of the molecule has a cyclic geometry, the reaction progresses in a concerted fashion, and the bond orbitals involved in the reaction overlap in a continuous cycle at the transition state.

  3. Frontier molecular orbital theory - Wikipedia

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

    An electrocyclic reaction is a pericyclic reaction involving the net loss of a pi bond and creation of a sigma bond with formation of a ring. This reaction proceeds through either a conrotatory or disrotatory mechanism. In the conrotatory ring opening of cyclobutene, there are two electrons moving suprafacially (on the pi bond) and two moving ...

  4. Group transfer reaction - Wikipedia

    en.wikipedia.org/wiki/Group_transfer_reaction

    In organic chemistry, a group transfer reaction is a class of the pericyclic reaction where one or more groups of atoms is transferred from one molecule to another. Group transfer reactions can sometimes be difficult to identify when separate reactant molecules combine into a single product molecule (like in the ene reaction).

  5. Diels–Alder reaction - Wikipedia

    en.wikipedia.org/wiki/Diels–Alder_reaction

    In organic chemistry, the Diels–Alder reaction is a chemical reaction between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative. It is the prototypical example of a pericyclic reaction with a concerted mechanism.

  6. Woodward–Hoffmann rules - Wikipedia

    en.wikipedia.org/wiki/Woodward–Hoffmann_rules

    Thermolysis converts 1 to (E,E) geometric isomer 2, but 3 to (E,Z) isomer 4.. The Woodward–Hoffmann rules (or the pericyclic selection rules) [1] are a set of rules devised by Robert Burns Woodward and Roald Hoffmann to rationalize or predict certain aspects of the stereochemistry and activation energy of pericyclic reactions, an important class of reactions in organic chemistry.

  7. Category:Pericyclic reactions - Wikipedia

    en.wikipedia.org/wiki/Category:Pericyclic_reactions

    In organic chemistry, a pericyclic reaction is a type of organic reaction wherein the transition state of the molecule has a cyclic geometry. Wikimedia Commons has media related to Pericyclic reactions .

  8. Möbius–Hückel concept - Wikipedia

    en.wikipedia.org/wiki/Möbius–Hückel_concept

    Thus it was noted that along the reaction coordinate of pericyclic processes one could have either a Möbius or a Hückel array of basis orbitals. With 4n or 4n + 2 electrons, one is then led to a prediction of allowedness or forbiddenness. Additionally, the M–H mnemonics give the MOs at part reaction. At each degeneracy there is a crossing ...

  9. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    In the pericyclic transition state, a small molecule donates two electrons to the ring. The reaction process can be shown using two different geometries, the small molecule can approach in a linear or non-linear fashion. In the linear approach, the electrons in the orbital of the small molecule are pointed directly at the π-system.