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  2. 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.

  3. C3H6O - Wikipedia

    en.wikipedia.org/wiki/C3H6O

    The molecular formula C 3 H 6 O may refer to: . Chemistry portal; Alcohols. Allyl alcohol or 2-propen-1-ol, CH 2 =CH-CH 2 OH, CAS number 107-18-6; cyclopropanol or cyclopropyl alcohol, cyclo (-CH 2-CH 2-HOHC-), CAS number 16545-68-9

  4. Acetylacetone - Wikipedia

    en.wikipedia.org/wiki/Acetylacetone

    The equilibrium constant tends to be high in nonpolar solvents; when K keto→enol is equal or greater than 1, the enol form is favoured. The keto form becomes more favourable in polar, hydrogen-bonding solvents, such as water. [7] The enol form is a vinylogous analogue of a carboxylic acid. [citation needed]

  5. Propylene oxide - Wikipedia

    en.wikipedia.org/wiki/Propylene_oxide

    Propylene oxide is an extremely flammable liquid, and its vapors can form explosive mixtures with air at concentrations as low as 2.3% (Lower Explosive Limit). [25] Propylene oxide vapor is twice as dense as air.

  6. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    In the presence of suitable catalysts, two acetone molecules also combine to form the compound diacetone alcohol (CH 3)C=O(CH 2)C(OH)(CH 3) 2, which on dehydration gives mesityl oxide (CH 3)C=O(CH)=C(CH 3) 2. This product can further combine with another acetone molecule, with loss of another molecule of water, yielding phorone and other ...

  7. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    Functional isomers are structural isomers which have different functional groups, resulting in significantly different chemical and physical properties. [ 11 ] An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3 : the first has a –C(=O)H functional group, which makes it an aldehyde , whereas the second has ...

  8. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    Isomers do not necessarily share similar chemical or physical properties. Two main forms of isomerism are structural (or constitutional) isomerism, in which bonds between the atoms differ; and stereoisomerism (or spatial isomerism), in which the bonds are the same but the relative positions of the atoms differ. Isomeric relationships form a ...

  9. File:C3H6O isomers.svg - Wikipedia

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

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