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  2. Tosyl group - Wikipedia

    en.wikipedia.org/wiki/Tosyl_group

    Tosyl group (blue) with a generic "R" group attached Tosylate group with a generic "R" group attached. Note the extra oxygen, compared to plain tosyl. In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos [nb 1]) is a univalent functional group with the chemical formula −SO 2 −C 6 H 4 −CH 3.

  3. p-Toluenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/P-Toluenesulfonic_acid

    p-Toluenesulfonic acid (PTSA, pTSA, or pTsOH) or tosylic acid (TsOH) is an organic compound with the formula CH 3 C 6 H 4 SO 3 H.It is a white extremely hygroscopic solid that is soluble in water, alcohols, and other polar organic solvents. [6]

  4. Sulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Sulfuric_acid

    Although nearly 100% sulfuric acid solutions can be made, the subsequent loss of SO 3 at the boiling point brings the concentration to 98.3% acid. The 98.3% grade, which is more stable in storage, is the usual form of what is described as "concentrated sulfuric acid".

  5. Structural chemistry - Wikipedia

    en.wikipedia.org/wiki/Structural_chemistry

    The determination of chemical structure include (mainly): for the gaseous state: gas electron diffraction [ 2 ] and microwave spectroscopy [ 3 ] for the liquid state: NMR spectroscopy [ 4 ] (note, obtaining precise structural information from liquids and solutions is still rather difficult compared to gases and crystalline solids)

  6. Hydrazine sulfate - Wikipedia

    en.wikipedia.org/wiki/Hydrazine_sulfate

    Hydrazine sulfate has a number of uses in chemical laboratories and in the chemical industry, including analytical chemistry and the synthesis of organic compounds. In those uses it is usually preferred to pure hydrazine, because it is not volatile and is less susceptible to atmospheric oxidation on storage.

  7. Hydroxylamine-O-sulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Hydroxylamine-O-sulfonic_acid

    [12] Synthesis of 1-Aminopyridin with HOSA. From 1-aminopyridinium salts the photochemically active 1-N-iminopyridinium ylides are accessible by acylation. [13] The photochemical rearrangement of the obtained 1-N-iminipyridinium ylides leads in high yields to 1H-1,2-diazepines [14] Synthesis of 1,2-Diazepinen aus Iminopyridiniumyliden

  8. Sodium hydrosulfide - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydrosulfide

    Sodium hydrosulfide is the chemical compound with the formula NaSH. This compound is the product of the half-neutralization of hydrogen sulfide (H 2 S) with sodium hydroxide (NaOH). NaSH and sodium sulfide are used industrially, often for similar purposes. Solid NaSH is colorless.

  9. Fluorosulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Fluorosulfuric_acid

    Fluorosulfuric acid (IUPAC name: sulfurofluoridic acid) is the inorganic compound with the chemical formula HSO 3 F.It is one of the strongest acids commercially available. It is a tetrahedral molecule and is closely related to sulfuric acid, H 2 SO 4, substituting a fluorine atom for one of the hydroxyl groups.