My professor posted this question as practice in naming compounds and provided the answer. I have stared at this for 30 minutes and cannot seem to figure out how he got this name out of it... Can someone please explain.
closed as off-topic by NotEvans., Todd Minehardt, Jan, Klaus-Dieter Warzecha, paracetamol Feb 5 '17 at 4:58
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The names that are proposed in the question are in accordance with obsolete IUPAC recommendations:
- 2-ethyl-5,5-dimethyl-1-hexene (1979 recommendations)
- 2-ethyl-5,5-dimethylhex-1-ene (1993 recommendations)
The corresponding rule in the 1979 recommendations is Rule A-3.4:
3.4 – Unsaturated branched acyclic hydrocarbons are named as derivatives of the unbranched hydrocarbons which contain the maximum number of double and triple bonds. If there are two or more chains competing for selection as the chain with the maximum number of unsaturated bonds, then the choice goes to (1) that one with the greatest number of carbon atoms; (2) the number of carbon atoms being equal, that one containing the maximum number of double bonds. In other respects, the same principles apply as for naming saturated branched acyclic hydrocarbons. The chain is so numbered as to give the lowest possible numbers to double and triple bonds in accordance with Rule A-3.3.
Therefore, the parent structure is the unbranched chain that contains the maximum number of double and triple bonds (here: one double bond). Since there is still a choice, the parent structure is the longest chain that contains the double bond, i.e. hexene. Numbering starts at the end of the chain that gives the lowest numbers to the double bond, i.e. 1-hexene. The 1-hexene is substituted using the usual principles of substitutive nomenclature, which yields 2-ethyl-5,5-dimethyl-1-hexene.
According to the 1993 recommendations, locants are placed immediately before the part of the name to which they relate. Therefore, the name 2-ethyl-5,5-dimethyl-1-hexene is changed to 2-ethyl-5,5-dimethylhex-1-ene.
The current version of Nomenclature of Organic Chemistry – IUPAC Recommendations and Preferred Names 2013 (Blue Book) incorporates a major change from earlier recommendations given in 1979 and 1993.
In acyclic parent structures the order of seniority between unsaturation and length of chain given in earlier recommendations is reversed. Thus, the first criterion to be considered in choosing a preferred parent acyclic chain is the length of the chain; unsaturation is now the second.
Therefore, the parent structure of the compound that is given in the question is now the longest chain, i.e. heptane. The heptane is substituted using the usual principles of substitutive nomenclature; i.e. the prefixes (here: ‘methyl’ and ‘methylidene’) are considered together in a series of increasing numerical order. This yields the preferred IUPAC name 2,2-dimethyl-5-methylideneheptane rather than 6,6-dimethyl-3-methyleneheptane since the locant set ‘2,2,5’ is lower than ‘3,6,6’.