key term - Stereoisomers

Definition

Stereoisomers are molecules that have the same molecular formula and connectivity, but differ in the three-dimensional arrangement of their atoms in space. This spatial arrangement of atoms leads to different physical and chemical properties, even though the atoms are connected in the same way.

5 Must Know Facts For Your Next Test

1. Stereoisomers arise due to the tetrahedral arrangement of atoms around a carbon center, which can lead to different spatial orientations of substituents.
2. Chirality, the property of a molecule to be non-superimposable on its mirror image, is the underlying cause of stereoisomerism.
3. Optical activity, the ability of a molecule to rotate the plane of polarized light, is a consequence of stereoisomerism and is used to distinguish enantiomers.
4. Pasteur's discovery of enantiomers in tartaric acid was a significant milestone in the understanding of stereoisomerism.
5. The Cahn-Ingold-Prelog sequence rules are used to specify the configuration of stereoisomers, allowing for unambiguous identification.

Review Questions

• Explain how the tetrahedral arrangement of atoms around a carbon center leads to the formation of stereoisomers.
  • The tetrahedral arrangement of atoms around a carbon center, with four different substituents, results in the possibility of multiple spatial orientations of these substituents. This leads to the formation of stereoisomers, which are molecules that have the same molecular formula and connectivity but differ in the three-dimensional arrangement of their atoms. The tetrahedral geometry allows for the creation of non-superimposable mirror images, known as enantiomers, as well as other types of stereoisomers, such as diastereomers and meso compounds.
• Describe the concept of chirality and its relationship to the optical activity of stereoisomers.
  • Chirality is the property of a molecule to be non-superimposable on its mirror image. Chiral molecules, such as enantiomers, have the ability to rotate the plane of polarized light, a phenomenon known as optical activity. This optical activity arises from the different spatial arrangements of the atoms in the chiral molecules, which interact with light in a unique way. The ability to rotate the plane of polarized light is a key characteristic used to distinguish enantiomers and understand the stereochemistry of molecules.
• Discuss the significance of Pasteur's discovery of enantiomers in tartaric acid and how it contributed to the understanding of stereoisomerism.
  • Pasteur's discovery of enantiomers in tartaric acid was a groundbreaking moment in the understanding of stereoisomerism. By physically separating the two forms of tartaric acid and observing their opposite optical activities, Pasteur demonstrated the existence of non-superimposable mirror images of the same molecule. This discovery challenged the prevailing belief that all molecules had a single, unique structure and paved the way for the concept of stereoisomerism. Pasteur's work highlighted the importance of the spatial arrangement of atoms and its impact on the physical and chemical properties of molecules, laying the foundation for the field of stereochemistry.

Related terms

Enantiomers:

Enantiomers are a type of stereoisomers that are non-superimposable mirror images of each other, possessing the same connectivity but differing in their spatial arrangement.

Diastereomers:

Diastereomers are stereoisomers that are not mirror images of each other, and they can have different physical and chemical properties.

Meso Compounds:

Meso compounds are a special type of stereoisomer that have a plane of symmetry, making them optically inactive despite containing chiral centers.