enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Propiolaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propiolaldehyde

    0.9152 g/cm 3: Boiling point: 54–57 °C (129–135 °F; 327–330 K) ... Its acetal can be prepared from acrolein. [2] Occurrence in interstellar medium

  3. Propionitrile - Wikipedia

    en.wikipedia.org/wiki/Propionitrile

    ch 3 ch 2 ch 2 oh + o 2 + nh 3 → ch 3 ch 2 c≡n + 3 h 2 o Propionitrile is a byproduct of the electrodimerisation of acrylonitrile to adiponitrile . In the laboratory propanenitrile can also be produced by the dehydration of propionamide , by catalytic reduction of acrylonitrile , or by distilling ethyl sulfate and potassium cyanide .

  4. 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.

  5. Propionaldehyde - Wikipedia

    en.wikipedia.org/wiki/Propionaldehyde

    The reflux condenser contains water heated at 60 °C, which condenses unreacted propanol, but allows propionaldehyde to pass. The propionaldehyde vapor is immediately condensed into a suitable receiver. In this arrangement, any propionaldehyde formed is immediately removed from the reactor, thus it does not get over-oxidized to propionic acid. [3]

  6. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    Alkyl hydrazones are 10 2 - to 10 3-fold more sensitive to hydrolysis than analogous oximes. [10] When derived from hydrazine itself, hydrazones condense with a second equivalent of a carbonyl to give azines: [11] R 2 C=N−NH 2 + R 2 C=O → R 2 C=N−N=CR 2 + H 2 O. Hydrazones are intermediates in the Wolff–Kishner reduction.

  7. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    The product, CH 3 CH(OCH 2 CH 3) 2, is formally named 1,1-diethoxyethane but is commonly referred to as "acetal". [39] This can cause confusion as "acetal" is more commonly used to describe compounds with the functional groups RCH(OR') 2 or RR'C(OR'') 2 rather than referring to this specific compound — in fact, 1,1-diethoxyethane is also ...

  8. 1,1-Diethoxyethane - Wikipedia

    en.wikipedia.org/wiki/1,1-Diethoxyethane

    1,1-Diethoxyethane (acetaldehyde diethyl acetal) is a major flavoring component of distilled beverages, especially malt whisky [3] and sherry. [4] Although it is just one of many compounds containing an acetal functional group, this specific chemical is sometimes called simply acetal .

  9. Knoevenagel condensation - Wikipedia

    en.wikipedia.org/wiki/Knoevenagel_condensation

    The active hydrogen component has the forms: [3] Z−CH 2 −Z or Z−CHR−Z for instance diethyl malonate, Meldrum's acid, ethyl acetoacetate or malonic acid, or cyanoacetic acid. [1] Z−CHRR', for instance nitromethane. where Z is an electron withdrawing group. Z must be powerful enough to facilitate deprotonation to the enolate ion even ...