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  2. Molecular graphics - Wikipedia

    en.wikipedia.org/wiki/Molecular_graphics

    A water molecule drawn with a shaded electrostatic potential isosurface. The areas highlighted in red have a net positive charge density , and the blue areas have a negative charge. In some models, the surface of the molecule is approximated and shaded to represent a physical property of the molecule, such as electronic charge density.

  3. Energy profile (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Energy_profile_(chemistry)

    Figure 6:Reaction Coordinate Diagrams showing reactions with 0, 1 and 2 intermediates: The double-headed arrow shows the first, second and third step in each reaction coordinate diagram. In all three of these reactions the first step is the slow step because the activation energy from the reactants to the transition state is the highest.

  4. Reaction coordinate - Wikipedia

    en.wikipedia.org/wiki/Reaction_coordinate

    Reaction coordinates are special order parameters that describe the entire pathway from reactants through transition states and on to products. Depending on the application, reaction coordinates may be defined by using chemically intuitive variables like bond lengths, or splitting probabilities (also called committors), or using the ...

  5. List of organic reactions - Wikipedia

    en.wikipedia.org/wiki/List_of_organic_reactions

    Algar–Flynn–Oyamada reaction; Alkylimino-de-oxo-bisubstitution; Alkyne trimerisation; Alkyne zipper reaction; Allan–Robinson reaction; Allylic rearrangement; Amadori rearrangement; Amine alkylation; Angeli–Rimini reaction; Andrussov oxidation; Appel reaction; Arbuzov reaction, Arbusow reaction; Arens–Van Dorp synthesis, Isler ...

  6. Arrow pushing - Wikipedia

    en.wikipedia.org/wiki/Arrow_pushing

    Arrow pushing or electron pushing is a technique used to describe the progression of organic chemistry reaction mechanisms. [1] It was first developed by Sir Robert Robinson.In using arrow pushing, "curved arrows" or "curly arrows" are drawn on the structural formulae of reactants in a chemical equation to show the reaction mechanism.

  7. Chemical reaction - Wikipedia

    en.wikipedia.org/wiki/Chemical_reaction

    Similar to the nucleophilic substitution, there are several possible reaction mechanisms that are named after the respective reaction order. In the E1 mechanism, the leaving group is ejected first, forming a carbocation. The next step, the formation of the double bond, takes place with the elimination of a proton (deprotonation). The leaving ...

  8. 19 detained for alleged home invasion at apartment Trump ...

    www.aol.com/news/19-detained-alleged-home...

    The viral images of the alleged gang members and further speculation elicited a response from Trump who in September during the presidential debate on ABC News said, "We have millions of people ...

  9. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Expressing resonance when drawing Lewis structures may be done either by drawing each of the possible resonance forms and placing double-headed arrows between them or by using dashed lines to represent the partial bonds (although the latter is a good representation of the resonance hybrid which is not, formally speaking, a Lewis structure).