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  2. Benzenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Benzenesulfonic_acid

    Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C 6 H 6 O 3 S.It is the simplest aromatic sulfonic acid.It forms white deliquescent sheet crystals or a white waxy solid that is soluble in water and ethanol, slightly soluble in benzene and insoluble in nonpolar solvents like diethyl ether.

  3. Phenylsulfinic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylsulfinic_acid

    By measuring the pK a at various ionic strengths and extrapolating to zero ionic strength, the pK a of phenylsulfinic acid was determined to be 2.76. [1] This makes phenylsulfinic acid a stronger acid than its corresponding carboxylic acid, benzoic acid (pK a = 4.2), but weaker than its corresponding sulfonic acid, benzenesulfonic acid (pK a ...

  4. Sulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfonic_acid

    General structure of a sulfonic acid with the functional group indicated in blue. In organic chemistry, sulfonic acid (or sulphonic acid) refers to a member of the class of organosulfur compounds with the general formula R−S(=O) 2 −OH, where R is an organic alkyl or aryl group and the S(=O) 2 (OH) group a sulfonyl hydroxide. [1]

  5. Sodium benzenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_benzenesulfonate

    Sodium benzenesulfonate is an organic compound with the formula C 6 H 5 SO 3 Na.It is white, water-soluble solid, It is produced by the neutralization benzenesulfonic acid with sodium hydroxide.

  6. Alkylbenzene sulfonate - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene_sulfonate

    In the most common route benzene is alkylated by long chain monoalkenes (e.g. dodecene) using hydrogen fluoride as a catalyst. [9] The purified dodecylbenzenes (and related derivatives) are then sulfonated with sulfur trioxide to give the sulfonic acid. [10] The sulfonic acid is subsequently neutralized with sodium hydroxide. [1]

  7. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    The simplest is phenol, C 6 H 5 OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule. Phenol – the simplest of the phenols Chemical structure of salicylic acid, the active metabolite of aspirin. Phenols are both synthesized industrially and produced by plants and ...

  8. Aromatic sulfonation - Wikipedia

    en.wikipedia.org/wiki/Aromatic_sulfonation

    In the Tyrer sulfonation process (1917), [7] at some time of technological importance, benzene vapor is led through a vessel containing 90% sulfuric acid the temperature of which is increased from 100 to 180°C. Water and benzene are continuously removed and the benzene fed back to the vessel. In this way an 80% yield is obtained.

  9. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula C 6 H 5 OH. [5] It is a white crystalline solid that is volatile. The molecule consists of a phenyl group (−C 6 H 5) bonded to a hydroxy group (−OH). Mildly acidic, it requires careful handling because it can cause ...