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  2. 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". Other concentrations are used for different purposes.

  3. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  4. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    An alternative, involving the formation of an acylium ion, becomes more important when the reaction takes place in concentrated acid (>90% sulfuric acid). [7] (In the Curtius rearrangement, sodium azide and an acyl chloride are combined to quantitatively generate the acyl azide intermediate, and the rest of the reaction takes place under ...

  5. 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.

  6. Aromatic sulfonation - Wikipedia

    en.wikipedia.org/wiki/Aromatic_sulfonation

    Sulfonation takes place in concentrated acidic conditions and desulfonation is the mode of action in a dilute hot aqueous acid. The reaction is very useful in protecting the aromatic system because of this reversibility. Due to their electron withdrawing effects, sulfonate protecting groups can be used to prevent electrophilic aromatic ...

  7. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The classic example of a dehydration reaction is the Fischer esterification, which involves treating a carboxylic acid with an alcohol to give an ester RCO 2 H + R′OH ⇌ RCO 2 R′ + H 2 O. Often such reactions require the presence of a dehydrating agent, i.e. a substance that reacts with water.

  8. Oleum - Wikipedia

    en.wikipedia.org/wiki/Oleum

    This means that sulfuric acid above said concentration will readily degenerate until it reaches 98.3%; this is impractical in some applications such as synthesis where anhydrous conditions are preferred (like alcohol eliminations). Adding sulfur trioxide alters the chemical equilibrium, allowing concentration to be increased beyond 98.3%.

  9. Kjeldahl method - Wikipedia

    en.wikipedia.org/wiki/Kjeldahl_method

    Hot concentrated sulfuric acid oxidizes carbon (as bituminous coal) and sulfur (see sulfuric acid's reactions with carbon): C + 2 H 2 SO 4 → CO 2 + 2 SO 2 + 2 H 2 O S + 2 H 2 SO 4 → 3 SO 2 + 2 H 2 O. Catalysts like selenium, Hg 2 SO 4 or CuSO 4 are often added to make the digestion go faster. Na 2 SO 4 or K 2 SO 4 is also added to increase ...