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  2. Phenylacetylene - Wikipedia

    en.wikipedia.org/wiki/Phenylacetylene

    Phenylacetylene is a prototypical terminal acetylene, undergoing many reactions expected of that functional group. It undergoes semi hydrogenation over Lindlar catalyst to give styrene . In the presence of base and copper(II) salts, it undergoes oxidative coupling to give diphenylbutadiyne . [ 6 ]

  3. Free body diagram - Wikipedia

    en.wikipedia.org/wiki/Free_body_diagram

    In physics and engineering, a free body diagram (FBD; also called a force diagram) [1] is a graphical illustration used to visualize the applied forces, moments, and resulting reactions on a free body in a given condition. It depicts a body or connected bodies with all the applied forces and moments, and reactions, which act on the body(ies).

  4. Phenylene group - Wikipedia

    en.wikipedia.org/wiki/Phenylene_group

    The chemical structure of the para-phenylene group.. In organic chemistry, the phenylene group (−C 6 H 4 −) is based on a di-substituted benzene ring ().For example, poly(p-phenylene) is a polymer built up from para-phenylene repeating units. [1]

  5. Diphenylacetylene - Wikipedia

    en.wikipedia.org/wiki/Diphenylacetylene

    Yet another method involves the coupling of iodobenzene and the copper salt of phenylacetylene in the Castro-Stephens coupling. The related Sonogashira coupling involves the coupling of iodobenzene and phenylacetylene. Diphenylacetylene is a planar molecule. The central C≡C distance is 119.8 picometers. [1]

  6. More O'Ferrall–Jencks plot - Wikipedia

    en.wikipedia.org/wiki/More_O'Ferrall–Jencks_plot

    In this type of plot (Figure 1), each axis represents a unique reaction coordinate, the corners represent local minima along the potential surface such as reactants, products or intermediates and the energy axis projects vertically out of the page. Changing a single reaction parameter can change the height of one or more of the corners of the plot.

  7. Alkynylation - Wikipedia

    en.wikipedia.org/wiki/Alkynylation

    These reactions invariably involve metal-acetylide intermediates. This reaction was discovered by chemist John Ulric Nef in 1899 while experimenting with reactions of elemental sodium, phenylacetylene, and acetophenone. [3] [4] For this reason, the reaction is sometimes referred to as Nef synthesis.

  8. Ariana Grande, Cynthia Erivo and why cruel body comments around 'Wicked' need to stop. She continued: "I've heard every version of it, of what's wrong with me, and then you fix it, and then it's ...

  9. 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.