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  2. 2-Pentyne - Wikipedia

    en.wikipedia.org/wiki/2-Pentyne

    Names Preferred IUPAC name. ... Chemical formula. C 5 H 8 Molar mass: 68.12 ... an organic compound with the formula CH 3 CH 2 C≡CCH 3 and is an internal alkyne.

  3. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    The general structure of an ether. R and R' represent most organyl substituents.. In organic chemistry, ethers are a class of compounds that contain an ether group—a single oxygen atom bonded to two separate carbon atoms, each part of an organyl group (e.g., alkyl or aryl).

  4. 3-Pentanone - Wikipedia

    en.wikipedia.org/wiki/3-Pentanone

    It can also be prepared by combining ethylene, CO, and H 2. [4] When the reaction is catalyzed by dicobalt octacarbonyl, water can be used as a source of hydrogen.A proposed intermediate is the ethylene-propionyl species [CH 3 C(O)Co(CO) 3 (ethylene)] which undergoes a migratory insertion to form [CH 3 COCH 2 CH 2 Co(CO) 3].

  5. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    Numerous organic compounds have other common names, often originating in historical source material thereof. 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.

  6. Methoxyethane - Wikipedia

    en.wikipedia.org/wiki/Methoxyethane

    Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula CH 3 OCH 2 CH 3. Unlike the related dimethyl ether and diethyl ether, which are widely used and studied, this mixed alkyl ether has no current applications. It is a structural isomer of isopropyl alcohol.

  7. Chemical nomenclature - Wikipedia

    en.wikipedia.org/wiki/Chemical_nomenclature

    The main purpose of chemical nomenclature is to disambiguate the spoken or written names of chemical compounds: each name should refer to one compound. Secondarily, each compound should have only one name, although in some cases some alternative names are accepted. Preferably, the name should also represent the structure or chemistry of a compound.

  8. Butanone - Wikipedia

    en.wikipedia.org/wiki/Butanone

    Butanone is the precursor to methyl ethyl ketone peroxide, which is a catalyst for some polymerization reactions such as crosslinking of unsaturated polyester resins. Dimethylglyoxime can be prepared from butanone first by reaction with ethyl nitrite to give diacetyl monoxime followed by conversion to the dioxime: [15]

  9. 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.