If you like us, please share us on social media, tell your friends, tell your professor or consider building or adopting a Wikitext for your course.

ChemWiki: The Dynamic Chemistry Hypertext > Core > Organic Chemistry > Fundamentals > Nomenclature > Omitting numbers in Nomenclature

Omitting numbers in Nomenclature

In naming organic chemicals, the nomenclature must specify the location of all special features. This is commonly done using "locants" such as numbers, as in 2-bromobutane. There are some cases where the number is omitted. However, students are sometimes confused about when they can omit a number. This page summarizes the cases where the number, most often a 1, can be omitted, and discusses a common misconception about when it can be omitted.


The general rule is that the locant (number) can be omitted when there is no ambiguity; that is, when only one location is possible. It cannot be omitted by making any assumption that a certain location is more likely.

The examples below are presented without showing the structures. All are simple compounds, and you should be able to draw them. In fact, this page will probably work best if you draw the structures for yourself as you go, so you can think about whether or not a number is required.

The cases where the number can be omitted can be considered in three classes:

  • Certain functional groups can only occur at a particular position, so simply stating the group defines the position unambiguously. The most common examples are the aldehyde and carboxylic acid groups, which can only be at the terminal C.
  • With (mono)-cyclic compounds carrying a single substituent, all positions are equivalent. The position of the substituent is defined as the 1-position, and is omitted from the name.
  • Some special cases with small molecules. These are actually special examples of one of the underlying ideas in the previous two cases, but are not as obvious.

Functional groups that define the position

The aldehyde and carboxylic acid functional groups can occur only at the end of a chain. When one of these is the main functional group, its position is defined as "1". Thus butanal (aldehyde) and butanoic acid (carboxylic acid) have the indicated functional group at the 1-position.

Similarly, butanedial and butanedioic acid have one functional group at each end; there is no other possibility, and the numbers are omitted.

Cyclic compounds with one substituent

All positions on a ring are equivalent. If there is one substituent, that substituent defines the "1" position. Thus bromocyclobutane and bromobenzene do not need numbers. There is only one possible compound of each name, and the bromo position is defined as "1".

This applies to single ring compounds, where all positions on the ring are equivalent.

Special cases

There are several chemicals, generally small ones, where the number for a substituent is commonly omitted, even though they do not quite fit one of the specific exceptions discussed above. However, they do fit the general criterion that the number is not needed, because there is no other choice. A list of some of those special cases follows. I encourage you to draw the structures, and be sure you agree that only one structure is possible in each case:

  • Methanol. Alcohols usually need a number, but there is only one C here, so no number is needed.
  • Ethanol. There are 2 C, but they are equivalent. There is only one alcohol possible based on ethane.
  • Ethene and propene. Double bonds usually need a number. But these cases are unambiguous simply because the molecule is small, and there is only one possible structure.
  • Propanone and butanone. Normally one would need to give a number for a ketone group. However, these two ketones are so small that they have only one possible ketone; the number is usually omitted. Note that with butanone, there are 4 C. However, two are terminal, so cannot be ketone C, and the other two are equivalent.
  • Methylpropane. Draw propane and then put on a methyl group. The only possible position is at 2, so the number in 2-methylpropane is often omitted. (If you added the methyl group at a terminal C, the compound would be butane, not methylpropane.)
  • Octachloropropane. There are only eight positions possible on propane, and "octachloro" means that all of them are Cl. One might write 1,1,1,2,2,3,3,3-octachloropropane, but the numbers are quite unnecessary, and usually omitted.


Sometimes people think that the 1 is a "default" number. That is, they think that the number 1 is implied if no number is given. Using this logic, they might give octanol or octene as (incorrect) names for 1-octanol or 1-octene. As you read the cases above where the number is omitted, it is important to realize that it is omitted because there is no other possibility, not because there is a default number. That is, one never "assumes" that a group is at "1".


A chemical name conveys information about the structure of the chemical; a name can be thought of as an "instruction manual" for how to draw the structure. When we first started discussing the nomenclature of organic compounds, we made the point that there are two types of wrong names. One type of incorrect name fails to provide the correct information. Another type of incorrect name may provide the information, but not follow the official (IUPAC) "rules" for doing so.

As an example, consider the simple chemical 1-chloropropane. If someone names this chloropropane, they have failed to communicate what compound they mean (since the chloro could be at either the 1-position or the 2-position). If someone names it 3-chloropropane, it is quite clear what they mean, even though they have violated the naming rules (give the substituent the lowest possible number).

The first type of error is much more important, as it means the primary goal of naming -- communication of the structure -- has failed.

How is this relevant to the discussion of omitting numbers? Well, you can do more harm by omitting a number that is needed than by giving one that is not needed. If it doubt, include the number. Omit the number only when it is perfectly clear what the meaning is.


You must to post a comment.
Last modified
17:52, 10 Nov 2013


This page has no custom tags.


(not set)
Lower Divisional






This material is based upon work supported by the National Science Foundation under Grant Numbers 1246120, 1525057, and 1413739.

Creative Commons License Unless otherwise noted, content in the UC Davis ChemWiki is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 United States License. Permissions beyond the scope of this license may be available at copyright@ucdavis.edu. Questions and concerns can be directed toward Prof. Delmar Larsen (dlarsen@ucdavis.edu), Founder and Director. Terms of Use