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Sodium naphthalene is an organic salt with the chemical formula Na + [C 10 H 8] −. In the research laboratory, it is used as a reductant in the synthesis of organic, organometallic, and inorganic chemistry. It is usually generated in situ. When isolated, it invariably crystallizes as a solvate with ligands bound to Na +. [1]
Vinyl monomers have the formula CH 2 =CHR, the most important are styrene (R = C 6 H 5), butadiene (R = CH=CH 2), and isoprene (R = C(Me)=CH 2). A second major class of monomers are acrylate esters, such as acrylonitrile, methacrylate, cyanoacrylate, and acrolein. Other vinyl monomers include vinylpyridine, vinyl sulfone, vinyl sulfoxide, vinyl ...
With alkali metals, naphthalene forms the dark blue-green radical anion salts such as sodium naphthalene, Na + C 10 H − 8. The naphthalene anions are strong reducing agents. Naphthalene can be hydrogenated under high pressure in the presence of metal catalysts to give 1,2,3,4-tetrahydronaphthalene(C 10 H 12), also known as tetralin.
Lab notebook with the complete record of the experiments underlying a published paper. [1] Chemistry stencils that used to be used for drawing equipment in lab notebooks. A laboratory notebook ( colloq. lab notebook or lab book ) is a primary record of research .
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An Orsat gas analyser or Orsat apparatus is a piece of laboratory equipment used to analyse a gas sample (typically fossil fuel flue gas) for its oxygen, carbon monoxide and carbon dioxide content. Although largely replaced by instrumental techniques, the Orsat remains a reliable method of measurement and is relatively simple to use. [1]
Sodium atoms have 11 electrons, one more than the stable configuration of the noble gas neon. As a result, sodium usually forms ionic compounds involving the Na + cation. [1] Sodium is a reactive alkali metal and is much more stable in ionic compounds. It can also form intermetallic compounds and organosodium compounds.
The fluorine-to-carbon atomic ratio (F/C ratio) is reduced from PTFE's theoretical ratio of 2.0 to 0.2 or less, after exposure to sodium naphthalene for 1 minute. [ 6 ] [ 7 ] [ 8 ] The fluorine atoms are replaced with hydroxyl, carbonyl, and other functional groups which can form hydrogen bonds.