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  2. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    In organic chemistry, an alkyl group is an alkane missing one hydrogen. [1] The term alkyl is intentionally unspecific to include many possible substitutions. An acyclic alkyl has the general formula of −CnH2n+1. A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula −CnH2n−1 ...

  3. List of chemistry mnemonics - Wikipedia

    en.wikipedia.org/wiki/List_of_chemistry_mnemonics

    Cations are positively (+) charged ions while anions are negatively (−) charged. This can be remembered with the help of the following mnemonics. Cats have paws ⇔ Cations are pawsitive. [23] Ca+ion: The letter t in cation looks like a + (plus) sign. [24] An anion is a negative ion. (An egative ionAnion). [25]

  4. Alkylation - Wikipedia

    en.wikipedia.org/wiki/Alkylation

    Alkylation. Alkylation is a chemical reaction that entails transfer of an alkyl group. The alkyl group may be transferred as an alkyl carbocation, a free radical, a carbanion, or a carbene (or their equivalents). [1] Alkylating agents are reagents for effecting alkylation. Alkyl groups can also be removed in a process known as dealkylation.

  5. Quaternary ammonium cation - Wikipedia

    en.wikipedia.org/wiki/Quaternary_ammonium_cation

    Quaternary ammonium cation. The R groups may be the same or different alkyl or aryl groups. Also, the R groups may be connected. In organic chemistry, quaternary ammonium cations, also known as quats, are positively-charged polyatomic ions of the structure [NR 4] +, where R is an alkyl group, an aryl group [1] or organyl group.

  6. Wolff–Kishner reduction - Wikipedia

    en.wikipedia.org/wiki/Wolff–Kishner_reduction

    The final step of the Wolff–Kishner reduction is the collapse of the diimide anion 2 in the presence of a proton source to give the hydrocarbon via loss of dinitrogen to afford an alkyl anion 3, which undergoes rapid and irreversible acid-base reaction with solvent to give the alkane. Evidence for this high-energy intermediate was obtained by ...

  7. Anionic addition polymerization - Wikipedia

    en.wikipedia.org/wiki/Anionic_addition...

    anionic polymerization: An ionic polymerization in which the kinetic-chain carriers are anions. [1] In polymer chemistry, anionic addition polymerization is a form of chain-growth polymerization or addition polymerization that involves the polymerization of monomers initiated with anions. The type of reaction has many manifestations, but ...

  8. Cationic polymerization - Wikipedia

    en.wikipedia.org/wiki/Cationic_polymerization

    The association is strongest as a covalent bond and weakest when the pair exists as free ions. [6] In cationic polymerization, the ions tend to be in equilibrium between an ion pair (either tight or solvent-separated) and free ions. [2] The more polar the solvent used in the reaction, the better the solvation and separation of the ions.

  9. Ammonium lauryl sulfate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_lauryl_sulfate

    Ammonium lauryl sulfate (ALS) is the common name for ammonium dodecyl sulfate (CH 3 (CH 2) 10 CH 2 OSO 3 NH 4). The anion consists of a nonpolar hydrocarbon chain and a polar sulfate end group. The combination of nonpolar and polar groups confers surfactant properties to the anion: it facilitates dissolution of both polar and non-polar materials.