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  2. 4-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/4-Methylpyridine

    4-Methylpyridine is both isolated from coal tar and is synthesized industrially. It forms via the reaction of acetaldehyde and ammonia in the presence of an oxide catalyst. The method also affords some 2-methylpyridine. 4-Methylpyridine is of little intrinsic value but is a precursor to other commercially significant species, often of medicinal ...

  3. 3-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/3-Methylpyridine

    3-Methylpyridine or 3-picoline, is an organic compound with formula 3-CH 3 C 5 H 4 N. It is one of three positional isomers of methylpyridine, whose structures vary according to where the methyl group is attached around the pyridine ring. This colorless liquid is a precursor to pyridine derivatives that have applications in the pharmaceutical ...

  4. C6H7N - Wikipedia

    en.wikipedia.org/wiki/C6H7N

    4-Methylpyridine Index of chemical compounds with the same molecular formula This set index page lists chemical structure articles associated with the same molecular formula .

  5. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    The reaction with alkyl halides leads to alkylation of the nitrogen atom. This creates a positive charge in the ring that increases the reactivity of pyridine to both oxidation and reduction. The Zincke reaction is used for the selective introduction of radicals in pyridinium compounds (it has no relation to the chemical element zinc).

  6. 2-Methylpyridine - Wikipedia

    en.wikipedia.org/wiki/2-Methylpyridine

    2-Methylpyridine, or 2-picoline, is the compound described with formula C 6 H 7 N. 2-Picoline is a colorless liquid that has an unpleasant odor similar to pyridine. It is mainly used to make vinylpyridine and the agrichemical nitrapyrin .

  7. Reactivity series - Wikipedia

    en.wikipedia.org/wiki/Reactivity_series

    In chemistry, a reactivity series (or reactivity series of elements) is an empirical, calculated, and structurally analytical progression [1] of a series of metals, arranged by their "reactivity" from highest to lowest.

  8. Dewar reactivity number - Wikipedia

    en.wikipedia.org/wiki/Dewar_reactivity_number

    Dewar's reactivity number is then defined as = (+). Clearly, the smaller the value of N i, the less the destabilization energy in going towards the transition state and the more reactive the site. Thus, by computation of the molecular orbital coefficients it is possible to evaluate Dewar's number for all the sites and establish which one will ...

  9. Transition metal pyridine complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_pyridine...

    trans-[MCl 2 (pyridine) 4] n+ is a common type of transition metal pyridine complex. Chloro(pyridine)cobaloxime. Crabtree's catalyst.. Owing to the relatively wide C-N-C angle, the 2,6-hydrogen atoms interfere with the formation of [M(py) 6] z complexes.