Isomers: Geometric and Diastereometric Isomers

  • Thread starter Thread starter Stevo1925
  • Start date Start date
  • Tags Tags
    Geometric Isomers
Click For Summary
SUMMARY

The discussion clarifies the distinction between diastereomers and geometric isomers, specifically addressing the confusion surrounding these terms. Geometric isomers, such as Cis-2-Butene and Trans-2-Butene, have the same atoms arranged differently, while diastereomers involve molecules with multiple chirality centers, such as (R,R) and (R,S). Diastereomers differ from enantiomers, which are mirror images of each other, as diastereomers possess different chemical and physical properties. This understanding is crucial for anyone studying stereochemistry.

PREREQUISITES
  • Understanding of chirality and stereochemistry
  • Familiarity with geometric isomers and their examples
  • Knowledge of optical activity and enantiomers
  • Basic concepts of molecular structure and isomerism
NEXT STEPS
  • Study the properties and examples of geometric isomers in organic chemistry
  • Learn about stereochemical nomenclature, including R/S and E/Z designations
  • Explore the differences between diastereomers and enantiomers in detail
  • Investigate the impact of chirality on chemical reactivity and physical properties
USEFUL FOR

Chemistry students, organic chemists, and researchers focusing on stereochemistry and molecular structure will benefit from this discussion.

Stevo1925
Messages
1
Reaction score
0
What is the difference between Diastereomers and Geometric Stereomers?

Im a little confused on this one as I thought they were the same thing?

Stevo1925
 
Physics news on Phys.org
I assume by Geometric Stereomers, you mean Geometric Isomers. Correct me if I'm wrong.

Geometric Isomers usually have the same atoms hooked to the other same atoms, but in a different way. Cis-2-Butene and Trans-2-Butene are examples.

Diastereomers have to do with chirality, and are currently hazy in my head right now, but I think that it's when a molecule has two chirality centers, You have (R,R), (R,S), (S,R), (S,S). (R,R) and (R,S) are diastereomers (as are (S,R) and (S,S)), while (R,R) and (S,S) are stereoisomers.
 
Char. Limit said:
Diastereomers have to do with chirality, and are currently hazy in my head right now, but I think that it's when a molecule has two chirality centers, You have (R,R), (R,S), (S,R), (S,S). (R,R) and (R,S) are diastereomers (as are (S,R) and (S,S)), while (R,R) and (S,S) are stereoisomers.

Diastereomers and enatiomers are both stereoisomers (isomers that have to do with chirality). Diastereomers are stereoiosmers that aren't enatiomers. Enatiomers are exact mirror images of one another- that is all chiral centers have opposite optical configurations. So in your example of two chiral centers RR and SS form one enatiomeric pair and SR and RS form another pair. Any other two pairs would be diastereomers (RR and SR, SS and RS). Note that diastereomers can also refer to molecules with greater than 2 chiral centers (eg. RSRR and RRRS). Enatiomers are identical except for the fact that they rotate plane polarized light in opposite directions. Diasteromers, on the other hand, have different chemical and physical properties (melting point, solubility, etc.)
 

Similar threads

  • · Replies 2 ·
Replies
2
Views
2K
  • · Replies 2 ·
Replies
2
Views
3K
  • · Replies 3 ·
Replies
3
Views
4K
Replies
2
Views
4K
  • · Replies 3 ·
Replies
3
Views
4K
  • · Replies 4 ·
Replies
4
Views
2K
  • · Replies 8 ·
Replies
8
Views
3K
  • · Replies 1 ·
Replies
1
Views
4K
  • · Replies 4 ·
Replies
4
Views
16K
Replies
5
Views
3K