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  2. Element–reactant–product table - Wikipedia

    en.wikipedia.org/wiki/Elementreactant...

    An elementreaction–product table is used to find coefficients while balancing an equation representing a chemical reaction. Coefficients represent moles of a substance so that the number of atoms produced is equal to the number of atoms being reacted with. [1] This is the common setup: Element: all the elements that are in the reaction ...

  3. 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 ]

  4. Sulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Sulfuric_acid

    The hydration reaction of sulfuric acid is highly exothermic. [19] As indicated by its acid dissociation constant, sulfuric acid is a strong acid: H 2 SO 4 → H 3 O + + HSO − 4 K a1 = 1000 (pK a1 = −3) The product of this ionization is HSO − 4, the bisulfate anion. Bisulfate is a far weaker acid: HSO − 4 + H 2 O → H 3 O + + SO 2− 4 ...

  5. Aromatic sulfonation - Wikipedia

    en.wikipedia.org/wiki/Aromatic_sulfonation

    C 6 H 6 + H 2 SO 4 + SOCl 2 → C 6 H 5 SO 3 H + SO 2 + 2 HCl. Historically, mercurous sulfate has been used to catalyze the reaction. [3] Chlorosulfuric acid is also an effective agent: C 6 H 6 + HSO 3 Cl → C 6 H 5 SO 3 H + HCl. In contrast to aromatic nitration and most other electrophilic aromatic substitutions this reaction is reversible ...

  6. Bisulfite - Wikipedia

    en.wikipedia.org/wiki/Bisulfite

    This reaction is useful for the separation and purification of aldehydes. [7] The bisulfite adducts are charged and so are more soluble in polar solvents. The reaction can be reversed in base or strong acid. [8] Examples of such procedures are described for benzaldehyde, [9] 2-tetralone, [10] citral, [11] the ethyl ester of pyruvic acid [12 ...

  7. 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 → ...

  8. Sulfur compounds - Wikipedia

    en.wikipedia.org/wiki/Sulfur_compounds

    Sulfur polycations, S 8 2+, S 4 2+ and S 16 2+ are produced when sulfur is reacted with oxidising agents in a strongly acidic solution. [1] The colored solutions produced by dissolving sulfur in oleum were first reported as early as 1804 by C.F. Bucholz, but the cause of the color and the structure of the polycations involved was only ...

  9. Piranha solution - Wikipedia

    en.wikipedia.org/wiki/Piranha_solution

    Molecular models of the different molecules active in Piranha solution: peroxysulfuric acid (H 2 SO 5) and hydrogen peroxide (H 2 O 2). Piranha solution, also known as piranha etch, is a mixture of sulfuric acid (H 2 SO 4) and hydrogen peroxide (H 2 O 2). The resulting mixture is used to clean organic residues off substrates, for example ...