There are millions of possible objects that can be described in science, too many to create common
names for every one. As a response, a number of systems of
systematic names have been created.
These can be as simple as assigning a prefix and a number to each object (in which case they are a sort of catalog reference), or as complex as encoding the complete structure of the object in the name. Many systems combine some information about the named object with an extra sequence number to make it into a unique identifier[?].
Systematic names often co-exist with earlier common names assigned before the creation of any systematic naming system. For example, many common chemicals are still referred to by their common names, even by chemists.
To give an example of why this is so, consider this example. The names "caffeine" and "3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione" both describe the same chemical.
The systematic name encodes the structure and composition of the caffiene molecule in some detail, and provides an unambiguous reference to this compound, whereas the name "caffeine" just names it. These advantages make the systematic name far superior to the common name when absolute clarity and precision is required. However, even professional chemists will use the non-systematic name 99% of the time, because caffeine is a well-known common chemical with a unique structure.
- Single atom anions are named with an -ide prefix, for example H+ is hydride.
- Compounds with a positive ion (cation), the name of the compound is simply the element name, with an -ide ending. For example, NaCl is sodium chloride, and CaF2 is calcium fluoride.
- Cations able to take on more than one positive charge are labeled with Roman numerals in parenthesises. For example, Cu+ is copper (I), Cu2+ is copper (II). An older notation is to append -ous or -ic' to the root of the Latin name to name ions with a lesser or greater charge. Under this naming convention, Cu+ is cuprous and Cu2+ is cupric.
- Oxyanions (polyatomic anions containing oxygen) are named with -ite or -ate, for a lesser or greater quantity of oxygen. For example, NO2- is nitrite, while NO3- is nitrate. If four oxyanions are possible, the prefixes hypo- and per- are used.
- The prefix bi- is used to indicate the presense of a single hydrogen ion.
An ionic compound is named by its cation followed by its anion. See
polyatomic ions[?] for a list of possible ions. For cations that take on multiple charges, the charge is written in
Roman numerals - for example, Cu(NO
3)
2 is
copper(II) nitrate[?], because the charge of two
nitrate ions is 2*-1=-2, and since the net charge of the
ionic compound must be zero, the Cu ion has a 2+ charge. This compound is therefore copper(II) nitrate.
Hydrates are ionic compounds that have absorbed water. They are named as the ionic compound followed by a numerical prefix and
-hydrate. The prefixes used are listed below:
- 1 mono-
- 2 di-
- 3 tri-
- 4 tetra-
- 5 penta-
- 6 hexa-
- 7 hepta-
- 8 octa-
- 9 nona-
- 10 deca-
For example, CuSO
4*5H
2O is
copper sulfate pentahydrate because it has five water molecules.
Molecular compounds are named with a prefix (see list above) before each element. The more
electronegative element is written last and with an
-ide suffix. For example, CO
2 is
carbon dioxide, and CCl
4 is
carbon tetrachloride. There are some exceptions to the rule, however. Sometimes prefixes are shortened to make the name easier to say; for example, CO is
carbon monoxide (as opposed to
monooxide).
Acids are named by the anion they form when dissolved in water. If an acid forms an anion named
___ide, it is named
hydro___ic acid. For example,
hydrochlor
ic acid forms a chlor
ide anion. Secondly, anions with an
-ate suffix are formed from acids with an
-ic suffix are dissolved -- chlor
ic acid dissociates to chlor
ate anions in water. Thirdly, anions with an
-ite suffix are formed when acids with an
-ous suffix are dissolved in water; for example chlor
ous acid disassociates into chlor
ite anions.
See also:
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