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  2. Sulfuric acid - Wikipedia

    en.wikipedia.org/wiki/Sulfuric_acid

    In spite of the viscosity of the acid, the effective conductivities of the H 3 SO + 4 and HSO − 4 ions are high due to an intramolecular proton-switch mechanism (analogous to the Grotthuss mechanism in water), making sulfuric acid a good conductor of electricity. It is also an excellent solvent for many reactions.

  3. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    Beckmann reaction. The reaction mechanism for this reaction is based on a catalytic cycle with cyanuric chloride activating the hydroxyl group via a nucleophilic aromatic substitution. The reaction product is dislodged and replaced by new reactant via an intermediate Meisenheimer complex. Beckmann cyanuric acid cataly cycle

  4. 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).

  5. Acid catalysis - Wikipedia

    en.wikipedia.org/wiki/Acid_catalysis

    In these reactions, the conjugate acid of the carbonyl group is a better electrophile than the neutral carbonyl group itself. Depending on the chemical species that act as the acid or base, catalytic mechanisms can be classified as either specific catalysis and general catalysis. Many enzymes operate by general catalysis.

  6. Aromatic sulfonation - Wikipedia

    en.wikipedia.org/wiki/Aromatic_sulfonation

    In organic chemistry, aromatic sulfonation is an reaction in which a hydrogen atom on an arene is replaced by a sulfonic acid (−SO 2 OH) group. Together with nitration and chlorination, aromatic sulfonation is a widely used electrophilic aromatic substitutions. [1] Aryl sulfonic acids are used as detergents, dye, and drugs.

  7. Schmidt reaction - Wikipedia

    en.wikipedia.org/wiki/Schmidt_reaction

    Reaction mechanism for the amine formation from a carboxylic acid via Schmidt reaction. In the reaction mechanism for the Schmidt reaction of ketones, the carbonyl group is activated by protonation for nucleophilic addition by the azide, forming azidohydrin 3, which loses water in an elimination reaction to diazoiminium 5.

  8. 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 This reaction is the first step in the sulfur-iodine cycle to produce hydrogen .

  9. Carbon snake - Wikipedia

    en.wikipedia.org/wiki/Carbon_snake

    The carbon snake is a demonstration of the dehydration reaction of sugar by concentrated sulfuric acid. With concentrated sulfuric acid, granulated table sugar ( sucrose ) performs a degradation reaction which changes its form to a black solid-liquid mixture . [ 1 ]