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  2. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  3. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula CH 3 (whereas normal methane has the formula CH 4). In formulas, the group is often abbreviated as Me. This hydrocarbon group occurs in many organic compounds. It is a very stable group in ...

  4. Triatomic hydrogen - Wikipedia

    en.wikipedia.org/wiki/Triatomic_hydrogen

    Triatomic hydrogen or H 3 is an unstable triatomic molecule containing only hydrogen.Since this molecule contains only three atoms of hydrogen it is the simplest triatomic molecule [1] and it is relatively simple to numerically solve the quantum mechanics description of the particles.

  5. Conjugate (acid-base theory) - Wikipedia

    en.wikipedia.org/wiki/Conjugate_(acid-base_theory)

    If a chemical is a strong acid, its conjugate base will be weak. [3] An example of this case would be the splitting of hydrochloric acid HCl in water. Since HCl is a strong acid (it splits up to a large extent), its conjugate base (Cl −) will be weak. Therefore, in this system, most H + will be hydronium ions H 3 O +

  6. Homologation reaction - Wikipedia

    en.wikipedia.org/wiki/Homologation_reaction

    In organic chemistry, a homologation reaction, also known as homologization, is any chemical reaction that converts the reactant into the next member of the homologous series. A homologous series is a group of compounds that differ by a constant unit, generally a methylene ( −CH 2 − ) group.

  7. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    A typical example of a Lewis acid in action is in the Friedel–Crafts alkylation reaction. [5] The key step is the acceptance by AlCl 3 of a chloride ion lone-pair, forming AlCl − 4 and creating the strongly acidic, that is, electrophilic, carbonium ion. RCl +AlCl 3 → R + + AlCl − 4

  8. Acetoacetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetoacetic_acid

    Acetoacetic esters are used for the acetoacetylation reaction, which is widely used in the production of arylide yellows and diarylide dyes. [3] Although the esters can be used in this reaction, diketene also reacts with alcohols and amines to the corresponding acetoacetic acid derivatives in a process called acetoacetylation .

  9. Trihydrogen cation - Wikipedia

    en.wikipedia.org/wiki/Trihydrogen_cation

    The role that H + 3 plays in the gas-phase chemistry of the ISM is unparalleled by any other polyatomic ion. The trihydrogen cation is the simplest triatomic molecule, because its two electrons are the only valence electrons in the system. It is also the simplest example of a three-center two-electron bond system.