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  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  3. Butyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Butyraldehyde

    Butyraldehyde, also known as butanal, is an organic compound with the formula CH 3 (CH 2) 2 CHO. This compound is the aldehyde derivative of butane. It is a colorless flammable liquid with an unpleasant smell. It is miscible with most organic solvents.

  4. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    In a Lewis adduct, the Lewis acid and base share an electron pair furnished by the Lewis base, forming a dative bond. [1] In the context of a specific chemical reaction between NH 3 and Me 3 B, a lone pair from NH 3 will form a dative bond with the empty orbital of Me 3 B to form an adduct NH 3 •BMe 3.

  5. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O. Commonly abbreviated Ac 2 O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with ...

  6. Methyl radical - Wikipedia

    en.wikipedia.org/wiki/Methyl_radical

    It can also be produced by the reaction of methane with the hydroxyl radical: OH • + CH 4 → CH • 3 + H 2 O. This process begins the major removal mechanism of methane from the atmosphere. The reaction occurs in the troposphere or stratosphere. In addition to being the largest known sink for atmospheric methane, this reaction is one of the ...

  7. Arsenic triiodide - Wikipedia

    en.wikipedia.org/wiki/Arsenic_triiodide

    Hydrolysis occurs only slowly in water forming arsenic trioxide and hydroiodic acid. The reaction proceeds via formation of arsenous acid which exists in equilibrium with hydroiodic acid. The aqueous solution is highly acidic, pH of 0.1N solution is 1.1. It decomposes to arsenic trioxide, elemental arsenic and iodine when heated in air at 200 °C.

  8. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    The keto and enol tautomers of acetylacetone coexist in solution. The enol form has C 2v symmetry, meaning the hydrogen atom is shared equally between the two oxygen atoms. [4] In the gas phase, the equilibrium constant, K keto→enol, is 11.7, favoring the enol form.

  9. 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 ...