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.
Table of contents |
1.1 Naming Ionic Compounds
2 External Links1.2 Naming Hydrates 1.3 Naming Molecular Compounds 1.4 Naming Organic Compounds 1.5 Naming Acids |
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.
1. Single atom anions are named with an -ide prefix, for example H- is hydride.
2. Compounds with a positive ion (cation), the name of the compound is simply the kation's name (usually the same as the element's), followed by the anion. For example, NaCl is sodium chloride, and CaF2 is calcium fluoride.
3. 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.
4. 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: Hypochlorite is ClO-, Perchlorate is ClO4-,
5. The prefix bi- is used to indicate the presense of a single hydrogen ion, as in sodium bicarbonate
See also:
Chemical Names
Naming Ionic Compounds
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(NO3)2 is copper(II) nitrate, because the charge of two nitrate ions is 2 x -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.
Naming Hydrates
Hydrates are ionic compounds that have absorbed water. They are named as the ionic compound followed by a numerical prefix and -hydrate. The numerical prefixes used are listed below:
For example, CuSO4*5H2O is 'copper sulfate pentahydrate because it has five water molecules.Naming Molecular Compounds
Inorganic 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, CO2 is carbon dioxide, and CCl4 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).Naming Organic Compounds
The naming sceme for organic compounds is complex and still developing, as is knowledge of the compounds themselves. Where the parent structure is an alkane, a comprehensive system of names exists.Naming Acids
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, hydrochloric acid forms a chloride anion. Secondly, anions with an -ate suffix are formed from acids with an -ic suffix are dissolved -- chloric acid dissociates to chlorate anions in water. Thirdly, anions with an -ite suffix are formed when acids with an -ous suffix are dissolved in water; for example chlorous acid disassociates into chlorite anions.External Links