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  2. Aluminium chloride - Wikipedia

    en.wikipedia.org/wiki/Aluminium_chloride

    Aluminium chloride finds a wide variety of other applications in organic chemistry. [20] For example, it can catalyse the ene reaction, such as the addition of 3-buten-2-one (methyl vinyl ketone) to carvone: [21] It is used to induce a variety of hydrocarbon couplings and rearrangements. [22] [23]

  3. Metal halides - Wikipedia

    en.wikipedia.org/wiki/Metal_halides

    The halides are usually good σ- and good π-donors. These ligands are usually terminal, but they might act as bridging ligands as well. For example, the chloride ligands of aluminium chloride bridge two aluminium centers, thus the compound with the empirical formula AlCl 3 actually has the molecular formula of Al 2 Cl 6 under

  4. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    Also, there are no carbocation rearrangements, as the acylium ion is stabilized by a resonance structure in which the positive charge is on the oxygen. The viability of the Friedel–Crafts acylation depends on the stability of the acyl chloride reagent. Formyl chloride, for example, is too unstable to be isolated.

  5. Lewis acid catalysis - Wikipedia

    en.wikipedia.org/wiki/Lewis_Acid_Catalysis

    Two common modes of Lewis acid catalysis in reactions with polar mechanisms. In reactions with polar mechanisms, Lewis acid catalysis often involves binding of the catalyst to Lewis basic heteroatoms and withdrawing electron density, which in turn facilitates heterolytic bond cleavage (in the case of Friedel-Crafts reaction) or directly activates the substrate toward nucleophilic attack (in ...

  6. Arrow pushing - Wikipedia

    en.wikipedia.org/wiki/Arrow_pushing

    Arrow pushing or electron pushing is a technique used to describe the progression of organic chemistry reaction mechanisms. [1] It was first developed by Sir Robert Robinson.In using arrow pushing, "curved arrows" or "curly arrows" are drawn on the structural formulae of reactants in a chemical equation to show the reaction mechanism.

  7. Inner sphere electron transfer - Wikipedia

    en.wikipedia.org/wiki/Inner_sphere_electron_transfer

    Inner sphere electron transfer (IS ET) or bonded electron transfer [1] is a redox chemical reaction that proceeds via a covalent linkage—a strong electronic interaction—between the oxidant and the reductant reactants.

  8. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    The bromide ion acquires a positive formal charge. At this moment the halogen ion is called a " bromonium ion " or "chloronium ion", respectively. When the first bromine atom attacks the carbon–carbon π-bond, it leaves behind one of its electrons with the other bromine that it was bonded to in Br 2 .

  9. Chloride - Wikipedia

    en.wikipedia.org/wiki/Chloride

    A chloride ion is a structural component of some proteins; for example, it is present in the amylase enzyme. For these roles, chloride is one of the essential dietary mineral (listed by its element name chlorine). Serum chloride levels are mainly regulated by the kidneys through a variety of transporters that are present along the nephron. [19]