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  2. Pinnick oxidation - Wikipedia

    en.wikipedia.org/wiki/Pinnick_Oxidation

    For example, HOCl can react with double bonds in the organic reactant or product via a halohydrin formation reaction. To prevent interference from HOCl, a scavenger is usually added to the reaction to consume the HOCl as it is formed. For example, one can take advantage of the propensity of HOCl to undergo this addition reaction by adding a ...

  3. Hypochlorous acid - Wikipedia

    en.wikipedia.org/wiki/Hypochlorous_acid

    Hypochlorous acid is an inorganic compound with the chemical formula Cl O H, also written as HClO, HOCl, or ClHO. [2] [3] Its structure is H−O−Cl.It is an acid that forms when chlorine dissolves in water, and itself partially dissociates, forming a hypochlorite anion, ClO −.

  4. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    In certain kinds of alkene polymerization reactions, chain walking is an isomerization process that introduces branches into growing polymers. [citation needed] The trans isomer of resveratrol can be converted to the cis isomer in a photochemical reaction. [6] Thermal rearrangement of azulene to naphthalene has been observed. [7]

  5. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    The same is true when an alkene reacts with water in an additional reaction to form an alcohol that involves carbocation formation. The hydroxyl group (OH) bonds to the carbon that has the greater number of carbon-carbon bonds, while the hydrogen bonds to the carbon on the other end of the double bond, that has more carbon–hydrogen bonds.

  6. Addition reaction - Wikipedia

    en.wikipedia.org/wiki/Addition_reaction

    In organic chemistry, an addition reaction is an organic reaction in which two or more molecules combine to form a larger molecule called the adduct. [1] [2] An addition reaction is limited to chemical compounds that have multiple bonds. Examples include a molecule with a carbon–carbon double bond (an alkene) or a triple bond (an alkyne).

  7. Click chemistry - Wikipedia

    en.wikipedia.org/wiki/Click_chemistry

    These reaction partners can interact specifically with the strained alkene, staying bioorthogonal to endogenous alkenes found in lipids, fatty acids, cofactors and other natural products. [ 38 ] Alkene and azide [3+2] cycloaddition

  8. Polymerization - Wikipedia

    en.wikipedia.org/wiki/Polymerization

    As alkenes can polymerize in somewhat straightforward radical reactions, they form useful compounds such as polyethylene and polyvinyl chloride (PVC), [3] which are produced in high tonnages each year [3] due to their usefulness in manufacturing processes of commercial products, such as piping, insulation and packaging.

  9. Hydrolysis - Wikipedia

    en.wikipedia.org/wiki/Hydrolysis

    When a carbohydrate is broken into its component sugar molecules by hydrolysis (e.g., sucrose being broken down into glucose and fructose), this is recognized as saccharification. [2] Hydrolysis reactions can be the reverse of a condensation reaction in which two molecules join into a larger one and eject a water molecule. Thus hydrolysis adds ...