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  2. Skeletal formula - Wikipedia

    en.wikipedia.org/wiki/Skeletal_formula

    The skeletal formula of the antidepressant drug escitalopram, featuring skeletal representations of heteroatoms, a triple bond, phenyl groups and stereochemistry. The skeletal formula, line-angle formula, bond-line formula or shorthand formula of an organic compound is a type of molecular structural formula that serves as a shorthand representation of a molecule's bonding and some details of ...

  3. Chemical bonding of water - Wikipedia

    en.wikipedia.org/wiki/Chemical_bonding_of_water

    2 O is sp 3 hybridized in which the 2s atomic orbital and the three 2p orbitals of oxygen are hybridized to form four new hybridized orbitals which then participate in bonding by overlapping with the hydrogen 1s orbitals. As such, the predicted shape and bond angle of sp 3 hybridization is tetrahedral and 109.5°. This is in open agreement with ...

  4. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    It is a very stable group in most molecules. While the methyl group is usually part of a larger molecule, bonded to the rest of the molecule by a single covalent bond (−CH 3), it can be found on its own in any of three forms: methanide anion (CH − 3), methylium cation (CH + 3) or methyl radical (CH • 3).

  5. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    Each of the four bonds in the linkage has a bond order of about 1.5, and the two oxygen atoms equally share the negative charge. The acetylacetonate anion is a bidentate ligand . IUPAC recommended p K a values for this equilibrium in aqueous solution at 25 °C are 8.99 ± 0.04 ( I = 0), 8.83 ± 0.02 ( I = 0.1 M NaClO 4 ) and 9.00 ± 0.03 ( I ...

  6. 2-Butyne - Wikipedia

    en.wikipedia.org/wiki/2-butyne

    2-Butyne (dimethylacetylene, crotonylene or but-2-yne) is an alkyne with chemical formula CH 3 C≡CCH 3. Produced artificially, it is a colorless, volatile, pungent liquid at standard temperature and pressure .

  7. Grignard reagent - Wikipedia

    en.wikipedia.org/wiki/Grignard_reagent

    With easily deprotonated 1,3-diketones and related acidic substrates, the Grignard reagent RMgX functions merely as a base, giving the enolate anion and liberating the alkane RH. Grignard reagents also react with many "carbonyl-like" compounds and other electrophiles: Reactions of Grignard reagents with various electrophiles

  8. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3. It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium). In IUPAC nomenclature, an acetyl group is called an ethanoyl group.

  9. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    A hydroxyl group (OH −) attaches to one carbon of the double bond, and a proton (H +) adds to the other. The reaction is highly exothermic. In the first step, the alkene acts as a nucleophile and attacks the proton, following Markovnikov's rule. In the second step an H 2 O molecule bonds to the other, more