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  2. 2,4-Dinitrotoluene - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrotoluene

    Six positional isomers are possible for dinitrotoluene. The most common one is 2,4-dinitrotoluene. The nitration of toluene gives sequentially mononitrotoluene, DNT, and finally TNT. 2,4-DNT is the principal product from dinitration, the other main product being about 30% 1,3-DN2-T. The nitration of 4-nitrotoluene gives 2,4-DNT. [5]

  3. File:2,4-Dinitrotoluene acsv.svg - Wikipedia

    en.wikipedia.org/wiki/File:2,4-Dinitrotoluene...

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  4. Template reaction - Wikipedia

    en.wikipedia.org/wiki/Template_reaction

    The template effects emphasizes the pre-organization provided by the coordination sphere, although the coordination modifies the electronic properties (acidity, electrophilicity, etc.) of ligands. [1] An early example is the dialkylation of a nickel dithiolate: [2] The corresponding alkylation in the absence of a metal ion would yield polymers.

  5. File:2,4-Dinitrotoluol.svg - Wikipedia

    en.wikipedia.org/wiki/File:2,4-Dinitrotoluol.svg

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  6. Organotin chemistry - Wikipedia

    en.wikipedia.org/wiki/Organotin_chemistry

    Organotin compounds are those with tin linked to hydrocarbons. The compound on the picture is trimethyltin chloride, an example of organotin compounds.. Organotin chemistry is the scientific study of the synthesis and properties of organotin compounds or stannanes, which are organometallic compounds containing tin–carbon bonds.

  7. Corey–Fuchs reaction - Wikipedia

    en.wikipedia.org/wiki/Corey–Fuchs_reaction

    The Corey–Fuchs reaction, also known as the Ramirez–Corey–Fuchs reaction, is a series of chemical reactions designed to transform an aldehyde into an alkyne. The formation of the 1,1-dibromoolefins via phosphine-dibromomethylenes was originally discovered by Desai, McKelvie and Ramirez.

  8. Toluene diisocyanate - Wikipedia

    en.wikipedia.org/wiki/Toluene_diisocyanate

    Toluene diisocyanate (TDI) is an organic compound with the formula CH 3 C 6 H 3 (NCO) 2.Two of the six possible isomers are commercially important: 2,4-TDI (CAS: 584-84-9) and 2,6-TDI (CAS: 91-08-7). 2,4-TDI is produced in the pure state, but TDI is often marketed as 80/20 and 65/35 mixtures of the 2,4 and 2,6 isomers respectively.

  9. Reimer–Tiemann reaction - Wikipedia

    en.wikipedia.org/wiki/Reimer–Tiemann_reaction

    The direct formylation of aromatic compounds can be accomplished by various methods such as the Gattermann reaction, Gattermann–Koch reaction, Vilsmeier–Haack reaction, or Duff reaction; however, in terms of ease and safety of operations, the Reimer–Tiemann reaction is often the most advantageous route chosen in chemical synthesis.