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  2. Pyridinium perbromide - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_perbromide

    Pyridinium perbromide (also called pyridinium bromide perbromide, pyridine hydrobromide perbromide, or pyridinium tribromide) is an organic chemical composed of a pyridinium cation and a tribromide anion. It can also be considered as a complex containing pyridinium bromide—the salt of pyridine and hydrogen bromide—with an added bromine (Br ...

  3. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  4. Pyridine - Wikipedia

    en.wikipedia.org/wiki/Pyridine

    Boiling point: 115.2 °C (239.4 °F; 388.3 K) [4] Solubility in water. Miscible [4] ... Pyridine is a basic heterocyclic organic compound with the chemical formula C ...

  5. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: ... Pyridine: 115.3 [24] Dimethylacetamide: 166.1 [25 ...

  6. Pyridinium - Wikipedia

    en.wikipedia.org/wiki/Pyridinium

    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] As pyridine is often used as an organic base in chemical reactions, pyridinium salts are produced in many acid-base reactions.

  7. 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.

  8. Pyridine (data page) - Wikipedia

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

    Critical point: 619 K (346 °C), 5660 Pa Std enthalpy change of fusion, ... log 10 of Pyridine vapor pressure. Uses formula: ...

  9. Polar aprotic solvent - Wikipedia

    en.wikipedia.org/wiki/Polar_aprotic_solvent

    high boiling point, high toxicity pyridine: C 5 H 5 N 115 °C 13.3 0.982 g/cm 3: 2.22 reacts with protic and Lewis acids sulfolane: C 4 H 8 SO 2: 286 °C 43.3 1.27 g/cm 3: 4.8 high boiling point tetrahydrofuran: C 4 H 8 O 66 °C 7.6 0.887 g/cm 3: 1.75 polymerizes in presence of strong protic and Lewis acids