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Draw the structure, and save it as a ChemDraw file. If you drew the structure before applying any settings, then you need to select the object, open the "Object" menu and choose "Apply document settings from → ACS Document 1996". Then save it as a PNG file, to be read by an image editor such as GIMP or IrfanView (see below for details).
The following other wikis use this file: Usage on ca.wikipedia.org Bioetanol; Usage on ckb.wikipedia.org سووتەمەنی ئیسانۆل; سوتەمەنی ئیسانۆل
Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula CH 3 CH 2 OH.It is an alcohol, with its formula also written as C 2 H 5 OH, C 2 H 6 O or EtOH, where Et stands for ethyl.
The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are connected to one another. [1] The chemical bonding within the molecule is also shown, either explicitly or implicitly.
Often, the main problem with drawing chemical structures in inkscape is that it does not have a hexagonal matrix built in. One can use the polygon/star tool (make sure that it's set to "polygon", checkbox at top, and that it's set to 6 corners). Hold down "ctrl" while drawing the first hexagon to get the angles straight.
In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom. [ 3 ] [ 4 ] Alcohols range from the simple, like methanol and ethanol , to complex, like sugar alcohols and cholesterol .
In chemistry, the Fischer projection, devised by Emil Fischer in 1891, is a two-dimensional representation of a three-dimensional organic molecule by projection. Fischer projections were originally proposed for the depiction of carbohydrates and used by chemists, particularly in organic chemistry and biochemistry. The use of Fischer projections ...
In organic chemistry, a hemiacetal is a functional group the general formula R 1 R 2 C(OH)OR, where R 1, R 2 is a hydrogen atom or an organic substituent. They generally result from the nucleophilic addition of an alcohol (a compound with at least one hydroxy group ) to an aldehyde ( R−CH=O ) or a ketone ( R 2 C=O ) under acidic conditions.