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  2. Walsh diagram - Wikipedia

    en.wikipedia.org/wiki/Walsh_diagram

    Walsh Diagram of an HAH molecule. Walsh diagrams, often called angular coordinate diagrams or correlation diagrams, are representations of calculated orbital binding energies of a molecule versus a distortion coordinate (bond angles), used for making quick predictions about the geometries of small molecules.

  3. Walsh function - Wikipedia

    en.wikipedia.org/wiki/Walsh_function

    The system of Walsh functions is known as the Walsh system. It is an extension of the Rademacher system of orthogonal functions. [2] Walsh functions, the Walsh system, the Walsh series, [3] and the fast Walsh–Hadamard transform are all named after the American mathematician Joseph L. Walsh.

  4. File:Walsh diagram intro.svg - Wikipedia

    en.wikipedia.org/wiki/File:Walsh_diagram_intro.svg

    English: An introductory Walsh diagram, for a bent molecule becoming linear. Date: 22 November 2009, vectorized 02:39, 21 February 2018 (UTC) Source:

  5. Chemical bonding of water - Wikipedia

    en.wikipedia.org/wiki/Chemical_bonding_of_water

    The simple MO diagram of H 2 O is shown on the right. [2] [3] Following simple symmetry treatments, the 1s orbitals of hydrogen atom are premixed as a 1 and b 1. Orbitals of same symmetry and similar energy levels can then be mixed to form a new set of molecular orbitals with bonding, nonbonding, and antibonding characteristics. In the simple ...

  6. A. D. Walsh - Wikipedia

    en.wikipedia.org/wiki/A._D._Walsh

    Arthur Donald Walsh FRS FRSE FRIC (8 August 1916 – 23 April 1977) was a British chemist, who served as Professor of Chemistry at the University of Dundee. He is usually referred to as Donald Walsh. He was the creator of the Walsh diagram and Walsh's Rules. [1]

  7. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    The π-system's ability to rotate as the small molecule approaches is crucial in forming new bonds. The direction of rotation will be different depending on how many π-electrons are in the system. Shown below is a diagram of a two-electron fragment approaching a four-electron π-system using frontier molecular orbitals.

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  9. Yamaguchi esterification - Wikipedia

    en.wikipedia.org/wiki/Yamaguchi_esterification

    The Yamaguchi esterification is the chemical reaction of an aliphatic carboxylic acid and 2,4,6-trichlorobenzoyl chloride (TCBC, Yamaguchi reagent) to form a mixed anhydride which, upon reaction with an alcohol in the presence of stoichiometric amount of DMAP, produces the desired ester.