When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Acetone (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetone_(data_page)

    Download as PDF; Printable version; ... This page provides supplementary chemical data on acetone. Material Safety Data Sheet

  3. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone (>C=O).It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.

  4. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Download as PDF; Printable version; ... Data source; Aniline: 184.3 3.69 ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; ...

  5. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  6. Deuterated acetone - Wikipedia

    en.wikipedia.org/wiki/Deuterated_acetone

    Deuterated acetone is prepared by the reaction of acetone with heavy water, 2 H 2 O or D 2 O, in the presence of a base. In this case, the base used is deuterated lithium hydroxide : [ 1 ] In order to fully deuterate the acetone, the process is repeated several times, distilling off the acetone from the heavy water, and re-running the reaction ...

  7. Talk:Acetone (data page) - Wikipedia

    en.wikipedia.org/wiki/Talk:Acetone_(data_page)

    Talk: Acetone (data page) Add languages. ... Download QR code; Print/export Download as PDF; Printable version ...

  8. Acetonide - Wikipedia

    en.wikipedia.org/wiki/Acetonide

    General structure of a 1,2-acetonide. The diol is shown in blue, the acetone part in red. In organic chemistry, an acetonide is the functional group composed of the cyclic ketal of a diol with acetone. The more systematic name for this structure is an isopropylidene ketal. Acetonide is a common protecting group for 1,2- and 1,3-diols. [1]

  9. Iodoacetone - Wikipedia

    en.wikipedia.org/wiki/Iodoacetone

    The reaction of acetone and iodine produces iodoacetone. The reaction is typically acid catalysed and first order with respect to acetone and the acid catalyst: [3] [6] C 3 H 6 O + I 2 → HI + C 3 H 5 IO