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  2. Büchner funnel - Wikipedia

    en.wikipedia.org/wiki/Büchner_funnel

    It is commonly thought to be named after the Nobel Laureate Eduard Buchner (without umlaut), but it is actually named after the industrial chemist Ernst Büchner. [2] A Büchner funnel fitted with Sintered Disc made of Boro 3.3 Glass. Diagram of filtration set-up using a Büchner flask

  3. Büchner flask - Wikipedia

    en.wikipedia.org/wiki/Büchner_flask

    Büchner flask A Büchner funnel is attached to the flask via a black elastomer adapter. The hose barb is connected via vacuum hose to a vacuum source such as an aspirator. ...

  4. Buchner ring expansion - Wikipedia

    en.wikipedia.org/wiki/Buchner_ring_expansion

    The Buchner ring expansion is a two-step organic C-C bond forming reaction used to access 7-membered rings. The first step involves formation of a carbene from ethyl diazoacetate , which cyclopropanates an aromatic ring.

  5. Suction filtration - Wikipedia

    en.wikipedia.org/wiki/Suction_filtration

    Diagram of the vacuum filtration apparatus. By flowing through the aspirator, water will suck out the air contained in the vacuum flask and the Büchner flask.There is therefore a difference in pressure between the exterior and the interior of the flasks : the contents of the Büchner funnel are sucked towards the vacuum flask.

  6. Buchner ring enlargement - Wikipedia

    en.wikipedia.org/?title=Buchner_ring_enlargement&...

    move to sidebar hide. From Wikipedia, the free encyclopedia

  7. Berlese funnel - Wikipedia

    en.wikipedia.org/wiki/Berlese_funnel

    A funnel (E) contains a sample of soil or leaf litter (D), and a heat source (F), in this case an electric lamp (G), heats the sample. Animals escaping from the desiccation of the sample descend through a filter (C) into a preservative liquid (A) in a receptacle (B).

  8. Büchner–Curtius–Schlotterbeck reaction - Wikipedia

    en.wikipedia.org/wiki/Büchner–Curtius...

    The Buchner–Curtius–Schlotterbeck reaction is the reaction of aldehydes or ketones with aliphatic diazoalkanes to form homologated ketones. [1] It was first described by Eduard Buchner and Theodor Curtius in 1885 [ 2 ] and later by Fritz Schlotterbeck in 1907. [ 3 ]

  9. Ludwig Büchner - Wikipedia

    en.wikipedia.org/wiki/Ludwig_Büchner

    Büchner was born at Darmstadt on 29 March 1824. From 1842 to 1848 he studied physics, chemistry, botany, mineralogy, philosophy and medicine at the University of Giessen, where he graduated in 1848 with a dissertation entitled Beiträge zur Hall'schen Lehre von einem excitomotorischen Nervensystem (Contributions to the Hallerian Theory of an Excitomotor Nervous System).