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Topic: Generic radical nomeclature  (Read 1546 times)

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Offline mjpam

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Generic radical nomeclature
« on: September 16, 2013, 08:29:06 PM »
I can identify and name (with the correct priority) the fundamental organic functional groups. However, when it comes to specifying families of structures where the number of intervening carbons is not necessarily explicit, I get somewhat lost. I can recognize the constituent parts of the radical name, but am not at all clear how they are ordered with respect to the "nucleus".

For instance, when I want to reference a substituted naphthalene, I don't know whether
C12=CC=CC(C(=O)O[H])=C1C=CC=C2C(=O)[C*]N[C*]
is a carbonylalkylaminoalkylnapthalene carboxylic acid* or a alkylaminoalkylcarbonylnaphthalene carboxylix acid.

Is there a standard way of specifying genric structure (e.g., towards the "nucleus")?

*I know the IUPAC designated infix of a carbonyl is "oxo" but it is easily confused with the infix for ether "oxy", so I prefer "carbonyl" in this context.

Offline gianegizelle

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Re: Generic radical nomeclature
« Reply #1 on: September 18, 2013, 03:54:48 AM »
http://butane.chem.uiuc.edu/cyerkes/Chem104A_BFA05/Genchemref/nomenclature_rules.html


try this site a search maybe it can help you....its the IUPAC RULES

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