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- Q86421 subject Q8692179.
- Q86421 abstract "A Newman projection, useful in alkane stereochemistry, visualizes chemical conformations of a carbon-carbon chemical bond from front to back, with the front carbon represented by a dot and the back carbon as a circle (see below). The front carbon atom is called proximal, while the back atom is called distal. This type of representation is useful for assessing the torsional angle between bonds.A Sawhorse representation, on the other hand, views a carbon-carbon bond from an oblique angle. This type of representation makes it easy to visualize the molecule as a whole in 3-D.Other methods for depicting molecules are the Fischer projection, the Haworth projection and the Natta projection.This projection is named after Melvin Spencer Newman, an American chemist of The Ohio State University who introduced it in 1952.".
- Q86421 thumbnail Sawhorse_projection_butane_-sc.png?width=300.
- Q86421 wikiPageWikiLink Q1128023.
- Q86421 wikiPageWikiLink Q134192.
- Q86421 wikiPageWikiLink Q17011927.
- Q86421 wikiPageWikiLink Q309331.
- Q86421 wikiPageWikiLink Q44424.
- Q86421 wikiPageWikiLink Q749328.
- Q86421 wikiPageWikiLink Q830859.
- Q86421 wikiPageWikiLink Q846171.
- Q86421 wikiPageWikiLink Q8692179.
- Q86421 wikiPageWikiLink Q926930.
- Q86421 comment "A Newman projection, useful in alkane stereochemistry, visualizes chemical conformations of a carbon-carbon chemical bond from front to back, with the front carbon represented by a dot and the back carbon as a circle (see below). The front carbon atom is called proximal, while the back atom is called distal. This type of representation is useful for assessing the torsional angle between bonds.A Sawhorse representation, on the other hand, views a carbon-carbon bond from an oblique angle.".
- Q86421 label "Newman projection".
- Q86421 depiction Sawhorse_projection_butane_-sc.png.