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  2. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The Wittig reaction involves reaction of an aldehyde or ketone with a Wittig reagent (or phosphorane) of the type Ph 3 P=CHR to produce an alkene and Ph 3 P=O. The Wittig reagent is itself prepared easily from triphenylphosphine and an alkyl halide.

  3. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.

  4. Rearrangement reaction - Wikipedia

    en.wikipedia.org/wiki/Rearrangement_reaction

    In organic chemistry, a rearrangement reaction is a broad class of organic reactions where the carbon skeleton of a molecule is rearranged to give a structural isomer of the original molecule. [1] Often a substituent moves from one atom to another atom in the same molecule, hence these reactions are usually intramolecular. In the example below ...

  5. Evelyn effect - Wikipedia

    en.wikipedia.org/wiki/Evelyn_effect

    In general, if more than one alkene can be formed during dehalogenation by an elimination reaction, the more stable alkene is the major product. There are two types of elimination reactions, E1 and E2. An E2 reaction is a One step mechanism in which carbon-hydrogen and carbon-halogen bonds break to form a double bond. C=C Pi bond.

  6. 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.

  7. McMurry reaction - Wikipedia

    en.wikipedia.org/wiki/McMurry_reaction

    The McMurry reaction of benzophenone. The McMurry reaction is an organic reaction in which two ketone or aldehyde groups are coupled to form an alkene using a titanium chloride compound such as titanium(III) chloride and a reducing agent. The reaction is named after its co-discoverer, John E. McMurry.

  8. Propylene - Wikipedia

    en.wikipedia.org/wiki/Propylene

    Propylene resembles other alkenes in that it undergoes electrophilic addition reactions relatively easily at room temperature. The relative weakness of its double bond explains its tendency to react with substances that can achieve this transformation. Alkene reactions include: Polymerization and oligomerization; Oxidation; Halogenation ...

  9. 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).