-oate
The suffix -oate is the IUPAC nomenclature used in organic chemistry to form names of compounds formed from carboxylic acids. They are of two types:
- Formed by replacing the hydrogen atom in the –COOH by some other radical, usually an alkyl or aryl radical forming an ester. For example, methyl benzoate is a molecular compound with the structure C6H5–CO–O–CH3, and its condensed structural formula usually written as C6H5COOCH3.
- Formed by removing the hydrogen atom in the –COOH, producing an anion, which joins with a cation forming a salt. For example, the sodium benzoate is an ionic compound with the structure C6H5–CO–O− Na+, and its condensed structural formula usually written as C6H5CO2Na.
The suffix is derived from "-oic acid".
The most common examples of compounds named with the "oate" suffix are esters, like ethyl acetate, CH
3COOCH
2CH
3.
References
- International Union of Pure and Applied Chemistry Organic Chemistry Division Commission on Nomenclature of Organic Chemistry (1995). Panico, Robert; Powell, Warren H.; Richer, Jean-Claude (eds.). A Guide to IUPAC Nomenclature of Organic Compounds: Recommendations 1993 (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of Organic Chemistry) (2nd ed.). Oxford: Blackwell Scientific Publications. ISBN 9780632034888.
- International Union of Pure and Applied Chemistry Division of Chemical Nomenclature and Structure Representation (2014). Favre, Henri A.; Powell, Warren H. (eds.). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. Cambridge: Royal Society of Chemistry. doi:10.1039/9781849733069. ISBN 978-1-84973-306-9.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.