CHM210 Class 10/08
Introduction to Organic Chemistry Nomenclature
Basic Focus: Introduction to basic organic chemistry, specifically how to name alkanes and alkenes. Discussion to include key reactions with plans to carry the topics over multiple classes.
Nomenclature Rules for Alkanes and Alkenes
Rules for naming alkanes:
Identify the parent chain (the longest continuous chain of carbon atoms).
Indicate the position of the main functional group on the parent chain.
Start numbering the carbon chain to identify the substituents present.
Example:
When discussing alkenes, the parent chain must contain the double bond.
For example, pentane is transformed into pentene by dropping the 'a' in 'pentane' and adding 'ene', indicating double bond presence.
A five-carbon chain is designated as pentene.
Numbering of alkenes:
Number the chain from the end nearest to the first carbon with the double bond:
For example, numbering from carbon 1, we receive 1, 2, 3, 4, 5 for pentene, allowing you to determine the specific structure.
Resulting structure: When the double bond is between carbons 2 and 3, two-pentene is the correct nomenclature.
Alternative naming suggested: pent-2-ene (more fluidity suggested in pronunciation).
Substituent Groups:
Focus on methyl groups located at specific carbons:
If two methyl groups are on carbons 2 and 3, this is named 2,3-dimethyl-2-pentene.
Important to follow specific punctuation: commas between numbers and dashes between numbers and letters.
Cycloalkenes and Naming Convention
Special consideration for cycloalkenes (like cyclooctanes):
For cycloalkenes, the carbons participating in the double bond are always numbered 1 and 2.
The numbering around the ring should provide the lowest possible number for the substituents (first substituent gets the lowest number).
Example structure: cycl