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IUPAC naming conventions can be used to produce a systematic name. The key steps in the naming of more complicated branched alkanes are as follows: [9] Identify the longest continuous chain of carbon atoms; Name this longest root chain using standard naming rules; Name each side chain by changing the suffix of the name of the alkane from "-ane ...
For example, the simplest alkane is CH 4 methane, and the nine-carbon alkane CH 3 (CH 2) 7 CH 3 is named nonane. The names of the first four alkanes were derived from methanol, ether, propionic acid and butyric acid, respectively.
The following is a list of straight-chain alkanes, the total number of isomers of each (including branched chains), and their common names, sorted by number of carbon atoms. [ 1 ] [ 2 ] Number of C atoms
The rotation has the same magnitude but opposite senses for the two isomers, and can be a useful way of distinguishing and measuring their concentration in a solution. For this reason, enantiomers were formerly called "optical isomers". [8] [9] However, this term is ambiguous and is discouraged by the IUPAC. [10] [11]
Functional isomers are structural isomers which have different functional groups, resulting in significantly different chemical and physical properties. [ 11 ] An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3 : the first has a –C(=O)H functional group, which makes it an aldehyde , whereas the second has ...
Here are the lists of the isomers of alkanes. Pages in category "Lists of isomers of alkanes" The following 6 pages are in this category, out of 6 total.
Very often, cis–trans stereoisomers contain double bonds or ring structures. In both cases the rotation of bonds is restricted or prevented. [4] When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas when the substituents are oriented in opposing directions, the diastereomer is referred to as trans.
The compound with the formula (C 5 H 5) 2 Fe 2 (CO) 4 exists as three isomers in solution. In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of ...