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  2. Formate - Wikipedia

    en.wikipedia.org/wiki/Formate

    Hydrolysis of methyl formate gives formic acid and regenerates methanol: HCOOCH 3 → HCOOH + CH 3 OH. Formic acid is used for many applications in industry. Formate esters often are fragrant or have distinctive odors. Compared to the more common acetate esters, formate esters are less commonly used commercially because they are less stable. [5]

  3. Propyl group - Wikipedia

    en.wikipedia.org/wiki/Propyl_group

    In organic chemistry, a propyl group is a three-carbon alkyl substituent with chemical formula −CH 2 CH 2 CH 3 for the linear form. This substituent form is obtained by removing one hydrogen atom attached to the terminal carbon of propane . [ 1 ]

  4. Wikipedia:Molecular structure diagram - Wikipedia

    en.wikipedia.org/wiki/Wikipedia:Molecular...

    Some inorganic solids dissociate - or crack - into molecular species heating or upon dissolving, e.g. Aluminium chloride. In such cases it is helpful to depict both the molecular and the nonmolecular forms. Some important chemical species cannot be easily represented with simple pictures, e.g. hydrochloric acid and non-stoichiometric compounds.

  5. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).

  6. C4H8O2 - Wikipedia

    en.wikipedia.org/wiki/C4H8O2

    The molecular formula C 4 H 8 O 2 may refer to: Acetoin; cis-Butene-1,4-diol; ... Propyl formate; Isopropyl formate This page was last edited on 17 December 2021, at ...

  7. Isobutyl formate - Wikipedia

    en.wikipedia.org/wiki/Isobutyl_formate

    Isobutyl formate (2-methylpropyl methanoate) is an organic ester with the chemical formula C 5 H 10 O 2. It is formed by the Fischer esterification of isobutanol with formic acid, with the aid of an acid catalyst. It is used as a flavor and fragrance ingredient because of its odor which is sweet, ethereal, and slightly fruity. [2] [3]

  8. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Here is a sample molecule with the parent carbons numbered: For simplicity, here is an image of the same molecule, where the hydrogens in the parent chain are removed and the carbons are shown by their numbers: Now, following the above steps: The parent hydrocarbon chain has 23 carbons. It is called tricosa-.

  9. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Typically an alkyl is a part of a larger molecule. In structural formulae , the symbol R is used to designate a generic (unspecified) alkyl group. The smallest alkyl group is methyl , with the formula −CH 3 .