1 / 16

Configurational Isomers

Configurational Isomers. Constitutional Isomer. Different compounds with the same molecular formula (we’ve done this one!) Examples C 6 H 10. Stereoisomers. Differ only in the spatial orientation of atoms. Enantiomers.

rayya
Download Presentation

Configurational Isomers

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Configurational Isomers

  2. Constitutional Isomer • Different compounds with the same molecular formula (we’ve done this one!) • Examples C6H10

  3. Stereoisomers • Differ only in the spatial orientation of atoms

  4. Enantiomers • is one of two stereoisomers that are non-superposable complete mirror images of each other, much as one's left and right hands are "the same" but opposite.

  5. Diastereomers • Are stereoisomers that are not enantiomers • In another definition diastereomers are pairs of isomers that have opposite configurations at one or more of the chiral centers but are not mirror images of each other

  6. Diastereomers

  7. Chirality • Chiral – have one carbon with four different groups bonded to it. (optically active) • Possess “handedness” – mirror images which are not superimposave

  8. Achiral • Have no plane of symmetry, they are not mirror images which are superimposable

  9. How do we decide? • R/S System • E/Z System We must learn a system to assign priorities to the atoms or groups of atoms attached to the carbon atom

  10. Cahn, Ingold and Prelog Priority • Assign sequence priorities to the four substituents by looking at the atoms attached directly to the chiral center. • 1.  The higher the atomic number of the immediate substituent atom, the higher the priority. For example, H–  <  C–  <  N–  <  O–  <  Cl–. (Different isotopes of the same element are assigned a priority according to their atomic mass.)2.  If two substituents have the same immediate substituent atom, evaluate atoms progressively further away from the chiral center until a difference is found.For example, CH3–  <  C2H5–  <  ClCH2–  <  BrCH2–  <  CH3O–. 3.  If double or triple bonded groups are encountered as substituents, they are treated as an equivalent set of single-bonded atoms.For example, C2H5–  <  CH2=CH–  <  HC≡C–

  11. R/S Once the attached groups are arranged by priority we point the one with the least (4) priority away from you and then decide if the orientation of 123 is clockwise (R) or counterclockwise (S) .

  12. R/S Convention

  13. Fischer Projections

  14. E/Z • Orientation across a double bond • Better than cis/trans

  15. Fischer Projections

  16. Exchange Method

More Related