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  2. Sulfurous acid - Wikipedia

    en.wikipedia.org/wiki/Sulfurous_acid

    Sulfuric(IV) acid (United Kingdom spelling: sulphuric(IV) acid), also known as sulfurous (UK: sulphurous) acid and thionic acid, [citation needed] is the chemical compound with the formula H 2 SO 3. Raman spectra of solutions of sulfur dioxide in water show only signals due to the SO 2 molecule and the bisulfite ion, HSO − 3 . [ 2 ]

  3. Thiosulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Thiosulfuric_acid

    The decomposition products can include sulfur, sulfur dioxide, hydrogen sulfide, polysulfanes, sulfuric acid and polythionates, depending on the reaction conditions. [6] Anhydrous methods of producing the acid were developed by Max Schmidt: [6] [7] H 2 S + SO 3 → H 2 S 2 O 3 Na 2 S 2 O 3 + 2 HCl → 2 NaCl + H 2 S 2 O 3 HSO 3 Cl + H 2 S → ...

  4. Sulfur oxoacid - Wikipedia

    en.wikipedia.org/wiki/Sulfur_oxoacid

    3 O 2− 10: Pure disulfuric acid melts at 36 °C. Present in fuming sulfuric acid, oleum. Examples known for n = 1 and n = 2. Peroxymonosulfuric acid: H 2 SO 5 +6 Peroxomonosulfate, OOSO 23 "Caro's acid", a solid melting at 45 °C Peroxydisulfuric acid: H 2 S 2 O 8 +6 Peroxydisulfate, O 3 SOOSO 23 "Marshall's acid", a solid melting at ...

  5. Sulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Sulfuric_acid

    The sulfur trioxide is absorbed into 97–98% H 2 SO 4 to form oleum (H 2 S 2 O 7), also known as fuming sulfuric acid or pyrosulphuric acid. The oleum is then diluted with water to form concentrated sulfuric acid. H 2 SO 4 + SO 3 → H 2 S 2 O 7 H 2 S 2 O 7 + H 2 O → 2 H 2 SO 4

  6. Oleum - Wikipedia

    en.wikipedia.org/wiki/Oleum

    For example, 10% oleum can also be expressed as H 2 SO 4 ·0.13611SO 3, 1.13611SO 3 ·H 2 O or 102.25% sulfuric acid. The conversion between % acid and % oleum is: % = + % For x = 1 and y = 2 the empirical formula H 2 S 2 O 7 for disulfuric (pyrosulfuric) acid is obtained. Pure disulfuric acid is a solid at room temperature, melting at 36 °C ...

  7. Aromatic sulfonation - Wikipedia

    en.wikipedia.org/wiki/Aromatic_sulfonation

    Typical conditions involve heating the aromatic compound with sulfuric acid: [2] C 6 H 6 + H 2 SO 4 → C 6 H 5 SO 3 H + H 2 O. Sulfur trioxide or its protonated derivative is the actual electrophile in this electrophilic aromatic substitution. To drive the equilibrium, dehydrating agents such as thionyl chloride can be added: [2] C 6 H 6 + H 2 ...

  8. Marquis reagent - Wikipedia

    en.wikipedia.org/wiki/Marquis_reagent

    The United States Department of Justice method for producing the reagent is the addition of 100 mL of concentrated (95–98%) sulfuric acid to 5 mL of 40% formaldehyde. [1]: 12 Different compounds produce different color reactions. Methanol may be added to slow down the reaction process to allow better observation of the colour change.

  9. Piranha solution - Wikipedia

    en.wikipedia.org/wiki/Piranha_solution

    A typical mixture is 3 parts of concentrated sulfuric acid and 1 part of 30 wt. % hydrogen peroxide solution; [1] other protocols may use a 4:1 or even 7:1 mixture. A closely related mixture, sometimes called "base piranha", is a 5:1:1 mixture of water, ammonia solution ( NH 4 OH , or NH 3 (aq) ), and 30% hydrogen peroxide.

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