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  2. Sulfur dioxide - Wikipedia

    en.wikipedia.org/wiki/Sulfur_dioxide

    As a η 1-SO 2 (S-bonded planar) ligand sulfur dioxide functions as a Lewis base using the lone pair on S. SO 2 functions as a Lewis acids in its η 1-SO 2 (S-bonded pyramidal) bonding mode with metals and in its 1:1 adducts with Lewis bases such as dimethylacetamide and trimethyl amine.

  3. Bunsen reaction - Wikipedia

    en.wikipedia.org/wiki/Bunsen_Reaction

    The Bunsen reaction is a chemical reaction that describes water, sulfur dioxide, and iodine reacting to form sulfuric acid and hydrogen iodide: . 2H 2 O + SO 2 + I 2 → H 2 SO 4 + 2HI ...

  4. Metal sulfur dioxide complex - Wikipedia

    en.wikipedia.org/wiki/Metal_sulfur_dioxide_complex

    The O, O'-sulphinate and O-sulphinate are difficult to distinguish as they have stretching frequencies from 1085–1050 cm −1 and 1000–820 cm −1 or lower. The pathway involving the O , O' sulphinate can generally be ruled out if the original metal complex fulfilled the 18-electron rule because the two metal–oxygen bonds would exceed the ...

  5. Sulfurous acid - Wikipedia

    en.wikipedia.org/wiki/Sulfurous_acid

    Sulfurous acid is commonly known to not exist in its free state, and due to this, it is stated in textbooks that it cannot be isolated in the water-free form. [4] However, the molecule has been detected in the gas phase in 1988 by the dissociative ionization of diethyl sulfite. [5]

  6. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    For example, acetic acid is a weak acid which has a = 1.75 x 10 −5. Its conjugate base is the acetate ion with K b = 10 −14 / K a = 5.7 x 10 −10 (from the relationship K a × K b = 10 −14 ), which certainly does not correspond to a strong base.

  7. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    Hydration reaction mechanism from 1-methylcyclohexene to 1-methylcyclohexanol. Many alternative routes are available for producing alcohols, including the hydroboration–oxidation reaction , the oxymercuration–reduction reaction , the Mukaiyama hydration , the reduction of ketones and aldehydes and as a biological method fermentation .

  8. Sulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Sulfuric_acid

    Sulfuric acid is a colorless oily liquid, and has a vapor pressure of <0.001 mmHg at 25 °C and 1 mmHg at 145.8 °C, [16] and 98% sulfuric acid has a vapor pressure of <1 mmHg at 40 °C. [ 17 ] In the solid state, sulfuric acid is a molecular solid that forms monoclinic crystals with nearly trigonal lattice parameters.

  9. Disulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Disulfuric_acid

    Disulfuric acid (alternative spelling disulphuric acid) or pyrosulfuric acid (alternative spelling pyrosulphuric acid), also named oleum, is a sulfur oxoacid. [3] It is a major constituent of fuming sulfuric acid, oleum, and this is how most chemists encounter it.