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  2. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    Demethylation (the transfer of the methyl group to another compound) is a common process, and reagents that undergo this reaction are called methylating agents. Common methylating agents are dimethyl sulfate, methyl iodide, and methyl triflate. Methanogenesis, the source of natural gas, arises via a demethylation reaction. [8]

  3. List of unsolved problems in chemistry - Wikipedia

    en.wikipedia.org/wiki/List_of_unsolved_problems...

    This is a list of unsolved problems in chemistry. Problems in chemistry are considered unsolved when an expert in the field considers it unsolved or when several experts in the field disagree about a solution to a problem.

  4. 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.

  5. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The conversion of ethanol to ethylene is a fundamental example: [3] [4] CH 3 CH 2 OH → H 2 C=CH 2 + H 2 O. The reaction is accelerated by acid catalysts such as sulfuric acid and certain zeolites. These reactions often proceed via carbocation intermediates as shown for the dehydration of cyclohexanol. [5] Some alcohols are prone to dehydration.

  6. 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.

  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. Crotonic acid - Wikipedia

    en.wikipedia.org/wiki/Crotonic_acid

    Crotonic acid ((2E)-but-2-enoic acid) is a short-chain unsaturated carboxylic acid described by the formula CH 3 CH=CHCO 2 H. The name crotonic acid was given because it was erroneously thought to be a saponification product of croton oil. [2]

  9. Hydroxamic acid - Wikipedia

    en.wikipedia.org/wiki/Hydroxamic_acid

    The general structure of a hydroxamic acid. In organic chemistry, hydroxamic acids are a class of organic compounds having a general formula R−C(=O)−N(−OH)−R' bearing the functional group −C(=O)−N(−OH)−, where R and R' are typically organyl groups (e.g., alkyl or aryl) or hydrogen.