Would this be a picture of pentene?

  • Thread starter Thread starter Qube
  • Start date Start date
  • Tags Tags
    Picture
Click For Summary
SUMMARY

The discussion centers on the nomenclature of alkenes, specifically regarding the compound pentene. The location of the double bond is crucial for naming, as it affects the compound's classification as a substituted pentene or an isomer of hexene. The systematic name derived from the discussion is 4-methyl-2-pentene, following the established rules for numbering the carbon chain to ensure the double bond receives the lowest possible number. The participants confirm that proper nomenclature includes indicating the position of the double bond in the name.

PREREQUISITES
  • Understanding of organic chemistry nomenclature
  • Familiarity with alkenes and their structural characteristics
  • Knowledge of carbon chain identification and numbering
  • Basic grasp of isomerism in organic compounds
NEXT STEPS
  • Study the IUPAC nomenclature rules for organic compounds
  • Learn about the properties and reactions of alkenes
  • Explore the concept of isomerism, focusing on structural isomers
  • Research examples of substituted alkenes and their naming conventions
USEFUL FOR

Chemistry students, organic chemists, and educators seeking to deepen their understanding of alkene nomenclature and structural isomerism.

Qube
Gold Member
Messages
461
Reaction score
1

Homework Statement



Would this be a picture of pentene?

I'm unsure because of the location of the double bond - does the location of the double bond factor into naming alkenes?
 

Attachments

  • CropperCapture[13].png
    CropperCapture[13].png
    734 bytes · Views: 442
Physics news on Phys.org
Location of the double bond matters, just like the side chain matters. But yes, technically it is a substituted pentene. At the same time it is an isomer of hexene.
 
Borek said:
Location of the double bond matters, just like the side chain matters. But yes, technically it is a substituted pentene. At the same time it is an isomer of hexene.

Thank you! I looked up the nomenclature rules for alkenes and they are:

1) Find longest carbon chain. In this case that would be the 5-carbon chain (pentene).
2) Number longest carbon chain so that the double bonded carbons have the lowest numbers.
3) If the double-bonded carbons are equidistant from the ends, then number so that the first substituent has the lowest number.
4) Name substituents and and chain as appropriate (follow rules for alkanes now)
5) If more than one double bond is present, indicate positions using numbers and add appropriate suffixies (i.e. -diene). In this case there is only one double bond.

So would the systematic name be: 4-methyl-2-pentene? I numbered so that the double-bonded carbons get the lowest numbers. I also forgot to mention above that the position of the double bond must be mentioned in the systematic name.
 
Last edited:
Although you are right in nomenclature, I'd say in my personal opinion, you can put the number corresponding to the position of multiple bond after the root (chain length). This way, if there are both double and triple bond present, it looks tidy.

For eg. 4-methylpent-2-ene.
 

Similar threads

  • · Replies 3 ·
Replies
3
Views
4K
Replies
3
Views
4K
Replies
2
Views
2K
Replies
1
Views
10K
  • · Replies 1 ·
Replies
1
Views
2K
  • · Replies 1 ·
Replies
1
Views
3K
  • · Replies 2 ·
Replies
2
Views
2K
  • · Replies 4 ·
Replies
4
Views
5K
Replies
4
Views
2K
Replies
1
Views
5K