This document provides instructions for naming alkanes and alkenes according to IUPAC nomenclature rules. For alkanes, the parent chain is the longest continuous carbon chain, and substituents are designated by name and location. For alkenes, the parent chain contains the double bond, the suffix is changed to -ene, and the double bond location is indicated. Examples are given to demonstrate the nomenclature systems.
This document provides instructions for naming alkanes and alkenes according to IUPAC nomenclature rules. For alkanes, the parent chain is the longest continuous carbon chain, and substituents are designated by name and location. For alkenes, the parent chain contains the double bond, the suffix is changed to -ene, and the double bond location is indicated. Examples are given to demonstrate the nomenclature systems.
This document provides instructions for naming alkanes and alkenes according to IUPAC nomenclature rules. For alkanes, the parent chain is the longest continuous carbon chain, and substituents are designated by name and location. For alkenes, the parent chain contains the double bond, the suffix is changed to -ene, and the double bond location is indicated. Examples are given to demonstrate the nomenclature systems.
3) 3,5-DIMETHYLPENTANE NOT 4,6-DIMETHYLOCTANE 4) 2,2,4,5-TETRAMETHYLHEXANE NOT 2,3,5,5-TETRAMETHYLHEXANE 5) 4-ETHYL-4-METHYLOCTANE NOT 5-METHYL-5-METHYLOCTANE 6) 3-ETHYL-4-ISOPROPYL-5,7,9-TRIMETHYLDECANE Draw the Structure of the following compounds: A. 4-ETHYL-2-METHYLHEXANE a) PARENT: HEXANE 2 B. 2,2-DIMETHYLPENTANE A) 2,5-DIMETHYL-3-ETHYLOCTANE NOMENCLATURE (SYSTEM for NAMING) FOR ALKANES - For those alkanes w/c have branching determine the longest continuous chain of C atoms and the longest C chain. EX: The compound shown has a longest continuous chain of 7 C atoms and therefore, its parent name is heptane. In order to designate the position of the substituent (CH3), the longest chain is numbered as shown. The substituent is called methyl. The name being derived from the methane for the alkane CH4, where the ane ending is changed to yl. The name of the compound is 2- METHYLHEPTANE, the no. 2 designating the C atom on w/c the methyl group is attached. Always number the longest chain of C atoms in such a way that the substituents have the smallest numbers. The compound shown was numbered to give the methyl group position the smallest number. If the numbering has been right to left, the name would be 6- METHYLHEPTANE and is incorrect because the position of attachment for the methyl group is not the lowest no. possible. ALKENES/ OLEFINS: CnH2n - w/ double bonds C. Common System: named as derivatives of ethylene 3 Examples Common Name 1) CH2=CH2 ETHYLENE 2) 3) ETHYLETHYLENE 4) CH3CH=CHCH3 SYM-DIMETHYLETHYLENE 5) UNSYM-DIMETHYLETHYLENE 6) CH3CH2CH=CH2CH3 SYM-ETHYLMETHYLETHYLENE alphabetical 7) UNSYM-ETHYLMETHYLETHYLENE SYM- both are bonded to each C of same hybridization. UNSYM- different hybridization. D. IUPAC - select the longest HC chain containing the = bond - name as an alkane - change ane to ene - indicate position of double bond (=)