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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. C4H8O2 - Wikipedia

    en.wikipedia.org/wiki/C4H8O2

    Propyl formate; Isopropyl formate This page was last edited on 17 December 2021, at 09:53 (UTC). Text is available under the Creative Commons Attribution-ShareAlike ...

  4. 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 ]

  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. C5H10O2 - Wikipedia

    en.wikipedia.org/wiki/C5H10O2

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  7. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    The structure of 3-methylpentane is viewed as consisting of two parts. First, five atoms comprise the longest straight chain of carbon centers. The parent five-carbon compound is named pentane (highlighted blue). The methyl "substituent" or "group" is highlighted red.

  8. IUPAC nomenclature of organic chemistry - Wikipedia

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

    Cycloalkanes and aromatic compounds can be treated as the main parent chain of the compound, in which case the positions of substituents are numbered around the ring structure. For example, the three isomers of xylene CH 3 C 6 H 4 CH 3 , commonly the ortho- , meta- , and para- forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4 ...

  9. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    For example, butanol H 3 C−(CH 2) 3 −OH, methyl propyl ether H 3 C−(CH 2) 2 −O−CH 3, and diethyl ether (H 3 CCH 2 −) 2 O have the same molecular formula C 4 H 10 O but are three distinct structural isomers. The concept applies also to polyatomic ions with the same total charge. A classical example is the cyanate ion O=C=N − and ...