Search results
Results From The WOW.Com Content Network
Download as PDF; Printable version; In other projects ... move to sidebar hide. 2,3-Dimethylhexane Skeletal formula of 2,3-Dimethylhexane: Ball and stick model of 2,3 ...
In organic chemistry, hexene is a hydrocarbon with the chemical formula C 6 H 12. The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the " -ene " suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond .
For octahedral complexes of formula MX 4 Y 2, two isomers also exist. (Here M is a metal atom, and X and Y are two different types of ligands.) In the cis isomer, the two Y ligands are adjacent to each other at 90°, as is true for the two chlorine atoms shown in green in cis-[Co(NH 3) 4 Cl 2] +, at left.
2,3-Dimethyl-1-butene is an organic compound with the formula CH 2 =C(CH 3)CH(CH 3) 2. Like the other isomers of dimethylbutene, it is a colorless liquid. Together with 2,3-dimethyl-2-butene it can be produced by dimerization of propylene. It is a precursor to the commercial fragrance tonalide. [1]
3,3-Dimethylhexane is a colourless, odourless liquid, chemical compound in the family of hydrocarbons which has a formula of C 8 H 18. It is an isomer of octane , where two methylene hydrogens at the third position in a hexane molecule have been replaced with two methyl groups.
3,4-Dimethylhexane [Wikidata Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.
Download as PDF; Printable version; ... Skeletal formula of 2,3,4-trimethylpentane with some implicit hydrogens added: ... 2,3,4-Trimethylpentane is a branched alkane.
3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane. The enantiomers are (R)-3-methylhexane [3] and (S)-3-methylhexane. [4]