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Secondary is a term used in organic chemistry to classify various types of compounds (e. g. alcohols, https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Supplemental_Modules_(Organic_Chemistry)/Alcohols/Nomenclature_of_Alcohols alkyl halides, amines) or reactive intermediates (e. g. alkyl radicals, carbocations). An atom is considered secondary if it has two 'R' Groups attached to it. [1] An 'R' group is a carbon containing group such as a methyl (CH3). A secondary compound is most often classified on an alpha carbon (middle carbon) or a nitrogen. The word secondary comes from the root word 'second' which means two.
| Red highlighted central atoms in various groups of chemical compounds. Secondary central atoms compared with primary, tertiary and quaternary central atoms. | ||||
| primary | secondary | tertiary | quaternary | |
| Carbon atom in an alkane | | | | |
This nomenclature can be used in many cases and further used to explain relative reactivity. The reactivity of molecules varies with respect to the attached atoms. Thus, a primary, secondary, tertiary and quaternary molecule of the same function group will have different reactivities.
Secondary alcohols have the formula RCH(OH)R' where R and R' are organyl. [2]
| Primary | Secondary | Tertiary | Quaternary | |
| Alcohol | | | | does not exist |
A secondary amine has the formula RR'NH where R and R' are organyl.
| Primary | Secondary | Tertiary | Quaternary | |
| Amine | | | | |
Secondary amides have the formula RC(O)NHR' where R can be H or organyl and R' is organyl.[ citation needed ] which is the loss of the single proton bonded to the middle nitrogen.
| Primary | Secondary | Tertiary | Quaternary | |
| Amide | | | | does not exist |
Secondary phosphines have two 'R' groups attached to a phosphorus atom and again, a P-H bond. [3]
| Primary | Secondary | Tertiary | Quaternary | |
| Phosphine | | | | |
"Secondary" is a general term used in chemistry that can be applied to many molecules, even more than the ones listed here; the principles seen in these examples can be further applied to other functional group containing molecules. The ones shown above are common molecules seen in many organic reactions. By classifying a molecule as secondary it then be compared with a molecule of primary or tertiary nature to determine the relative reactivity.