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  2. C3H6O - Wikipedia

    en.wikipedia.org/wiki/C3H6O

    1,2-epoxy-propane or Propylene oxide or methyl oxirane, cyclo(-C*H(CH 3)-CH 2-O-), C* chiral, CAS number: 75-56-9 (R)-(+)-methyl oxirane, CAS number 15448-47-2

  3. Oxetane - Wikipedia

    en.wikipedia.org/wiki/Oxetane

    A typical well-known method of preparation is the reaction of potassium hydroxide with 3-chloropropyl acetate at 150 °C: [2]. Yield of oxetane made this way is c. 40%, as the synthesis can lead to a variety of by-products including water, potassium chloride, and potassium acetate.

  4. Cyclopropanol - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanol

    Cyclopropanol is an organic compound with the chemical formula C 3 H 6 O. It contains a cyclopropyl group with a hydroxyl group attached to it. The compound is highly unstable due to the three-membered ring, and is susceptible to reactions that open the ring.

  5. Propylene oxide - Wikipedia

    en.wikipedia.org/wiki/Propylene_oxide

    Propylene oxide is an acutely toxic and carcinogenic organic compound with the molecular formula C 3 H 6 O. This colourless volatile liquid with an odour similar to ether, is produced on a large scale industrially.

  6. Metamerism (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Metamerism_(Chemistry)

    The isomers which have been cited as examples of metamers in chemical literature consist primarily of ethers; [3] but this could by the same reasoning be extended to thioethers, secondary as well as tertiary amines, esters, secondary as well as tertiary amides, (mixed) acid anhydrides etc. Metamers in organic chemistry

  7. File:C3H6O isomers.svg - Wikipedia

    en.wikipedia.org/wiki/File:C3H6O_isomers.svg

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  8. Tolyl group - Wikipedia

    en.wikipedia.org/wiki/Tolyl_group

    Structures of the three isomers of tolyl group. In organic chemistry, tolyl groups are functional groups related to toluene. [1] They have the general formula CH 3 C 6 H 4 −R, the change of the relative position of the methyl and the R substituent on the aromatic ring can generate three possible structural isomers 1,2 (ortho), 1,3 (meta), and 1,4 (para).

  9. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.