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Nomenclature of organic compounds: IUPAC: International Union of Pure and Applied Chemistry Structure of IUPAC name: Seconary prefix Substituents Primary prefix Primary suffix Aliphatic/cyclic Stem (a) Primary suffix: Root word for the main carbon chain Number of carbon Root word atoms 1 Meth2 Eth3 Prop4 But(a)5 Pent(a)6 Hex(a)7 Hept(a)- Secondary suffix the most important functional group Number of carbon atoms 8 9 10 11 12 15 16 Root word Oct(a)Non(a)Dec(a)Undec(a)Dodec(a)Pentadec(a) Hexadec(a)- Types of hydrocarbon Alkane -an(e) Alkene -en(e) Alkyne -yn(e) (b) Primary prefix: (Space) Cyclo aliphatic cyclic compound (Space) aliphatic Cyclo cyclic compound Example: H H H HH Multiplying prefix: Number of the same group 2 3 4 5 ethyne C2 | alkyne Multiplying prefix diTriTetr(a)Pent(a)- H H H H H pentane C5 | alkane H H cyclohexene cyclic | C6 | alkene Number of the same group 6 7 8 9 Multiplying prefix Hex(a)Hept(a)Oct(a)Non(a)- Classwork: IUPAC name / page 1 Functional groups: Functional group *Cations Structure N Carboxylic acid Suffix Ammonium ion Prefix + -oic acid O OH SO3H *sulphonic acid Ester -sulphonic acid -oate O R R' O Acyl halide -oyl halide O X Amide -amide O NH2 Aldehyde O -al Oxo- -one Keto- -nitrile Cyano- -ol -amine halide HydroxyAminoHaloNitro- H Ketone O R R' Nitrile R N OH NH2 X NO2 Alcohol Amine halide Nitro compound (c) Secondary suffix: Determine which one is the most important functional group. Label the carbon atom(s) by means of lowest position series method. OH 1 Example: 6 OH 4 3 2 HO 1 2 2 3 5 3 4 4 1 butan-2-ol cyclohex-3-en-1-ol 4-methylphenol Classwork: OH O OH OH OH HO O IUPAC name / page 2 (d) Secondary prefix: Some common substitutents: RalkylCH3methylCH3CH2ethylFfluoroClchloroBrbromoIiodoOthers Refer to functional group table. IUPAC name / page 3