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  2. Pyridinium chloride - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chloride

    Containing a pyridinium ion, pyridinium chloride has a pK a of approximately 5, slightly more acidic than that of typical amines. This is due to the hybridization of the nitrogen: the nitrogen is sp 2 hybridized and more electronegative than those nitrogens in ammonium cations, which are sp 3 hybridized. Hence they are stronger acids than ...

  3. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    2-Chloropyridine is an aryl chloride with the formula C 5 H 4 ClN. It is a colorless liquid that is mainly used to generate fungicides and insecticides in industry. It also serves to generate antihistamines and antiarrythymics for pharmaceutical purposes. [2] It is one of three isomers of chloropyridine.

  4. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Pyridine-borane (C 5 H 5 NBH 3, melting point 10–11 °C) is a mild reducing agent. structure of the Crabtree's catalyst. Transition metal pyridine complexes are numerous. [108] [109] Typical octahedral complexes have the stoichiometry MCl 2 (py) 4 and MCl 3 (py) 3. Octahedral homoleptic complexes of the type M(py) + 6 are rare or tend to ...

  5. Pyridinium - Wikipedia

    en.wikipedia.org/wiki/Pyridinium

    Pyridinium refers to the cation [C 5 H 5 NH] +. It is the conjugate acid of pyridine. Many related cations are known involving substituted pyridines, e.g. picolines, lutidines, collidines. They are prepared by treating pyridine with acids. [3]

  6. 2-Bromopyridine - Wikipedia

    en.wikipedia.org/wiki/2-Bromopyridine

    2-Bromopyridine reacts with butyllithium to give 2-lithiopyridine, [2] which is a versatile reagent. [3] Pyrithione can be prepared in a two-step synthesis from 2-bromopyridine by oxidation to the N-oxide with a suitable peracid followed by substitution using either sodium dithionite or sodium sulfide with sodium hydroxide to introduce the thiol functional group.

  7. Pyridine (data page) - Wikipedia

    en.wikipedia.org/wiki/Pyridine_(data_page)

    115.4 Table data obtained from CRC Handbook of Chemistry and Physics 44th ed. log 10 of Pyridine vapor pressure. Uses formula: ...

  8. Morpholine - Wikipedia

    en.wikipedia.org/wiki/Morpholine

    Morpholine is a common additive, in parts per million concentrations, for pH adjustment in both fossil fuel and nuclear power plant steam systems. Morpholine is used because its volatility is about the same as water , so once it is added to the water, its concentration becomes distributed rather evenly in both the water and steam phases .

  9. Pyridinium chlorochromate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chlorochromate

    C 5 H 5 N + HCl + CrO 3 → [C 5 H 5 NH][CrO 3 Cl] In one alternative method, formation of toxic chromyl chloride (CrO 2 Cl 2 ) fumes during the making of the aforementioned solution were minimized by simply changing the order of addition: a cold solution of pyridine in concentrated hydrochloric acid was added to solid chromium trioxide under ...