1 / 44

Stereoisomers

Stereoisomers. All molecules have a mirror image – but for most molecules it is the same molecule. For some molecules the mirror image is a different molecule (the mirror image is non-superimposable). Left and right hands are an example of non-superimposable mirror images.

Download Presentation

Stereoisomers

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. Stereoisomers Dr Seemal Jelani Chem-261

  2. All molecules have a mirror image – but for most molecules it is the same molecule. Dr Seemal Jelani Chem-261

  3. For some molecules the mirror image is a different molecule (the mirror image is non-superimposable). Dr Seemal Jelani Chem-261

  4. Dr Seemal Jelani Chem-261

  5. Left and right hands are an example of non-superimposable mirror images. Dr Seemal Jelani Chem-261

  6. This usually happens when a molecule contains a C atom with four different groups attached (chiral / asymmetricC). • Such molecules are said to be chiral or optically active. Dr Seemal Jelani Chem-261

  7. The optical isomers are called enantiomers. • These are distinguished by +/-, D/L or more correctly R/S. • A 50/50 mixture of the two enantiomers is called a racemic mixture or a racemate. Dr Seemal Jelani Chem-261

  8. TASKWhich of the following molecules are optically active? • propan-2-ol • 2-chlorobutane • 1-chlorobutane • 3-methylhexane • butanone • 2-methylbutanoic acid • butan-2-ol • 1-chloro-3-methylpentane Dr Seemal Jelani Chem-261

  9. propan-2-ol NOT OPTICALLY ACTIVE Dr Seemal Jelani Chem-261

  10. 2-chlorobutane Dr Seemal Jelani Chem-261 OPTICALLY ACTIVE

  11. 1-chlorobutane NOT OPTICALLY ACTIVE Dr Seemal Jelani Chem-261

  12. 3-methylhexane Dr Seemal Jelani Chem-261 OPTICALLY ACTIVE

  13. butanone NOT OPTICALLY ACTIVE Dr Seemal Jelani Chem-261

  14. propan-2-ol NOT OPTICALLY ACTIVE Dr Seemal Jelani Chem-261

  15. 2-methylbutanoic acid Dr Seemal Jelani Chem-261 OPTICALLY ACTIVE

  16. butan-2-ol Dr Seemal Jelani Chem-261 OPTICALLY ACTIVE

  17. 1-chloro-3-methylpentane Dr Seemal Jelani Chem-261 OPTICALLY ACTIVE

  18. Molecules that are optical isomers are called enantiomers. • Enantiomers have identical chemical and physical properties, except: • Their effect on plane polarised light • Their reaction with other chiral molecules Dr Seemal Jelani Chem-261

  19. 2-Chlorobutane Dr Seemal Jelani Chem-261

  20. 3-Chlorocyclohexene Dr Seemal Jelani Chem-261

  21. Formula to calculate stereoisomers • For a molecule with 1 chiral center, 2x1 = 2 stereoisomers are possible • For a molecule with 2 chiral centers, a maximum of 2x2 = 4 stereoisomers are possible • For a molecule with n chiral centers, a maximum of 2n stereoisomers are possible Dr Seemal Jelani Chem-261

  22. Stereoisomers with tow chiral carbon atoms • Molecules with two similar chiral center gives • Enantiomers • Diastereomers and Meso compounds Dr Seemal Jelani Chem-261

  23. 2,3,4-Trihydroxybutanal • R S S R • two chiral centers • 22 = 4 stereoisomers exist; two pairs of enantiomers R (a) S (b) R (c) S (d) Dr Seemal Jelani Chem-261

  24. Maximum stereoisomers= 22 =4 • (a ) and (b) are non superposable mirror images of each other therefore they are a “pair of enantiomers” Dr Seemal Jelani Chem-261

  25. 2,3,4-Trihydroxybutanol exists in 2 pairs of enantiomer (a,b) and (c,d) • (a) = (2R,3R) erythrose • (b) = (2S,3S) erythrose • (c) = (2R,3S) threose • (d) = (2S,3R) threose Dr Seemal Jelani Chem-261

  26. Both erythrose and threose belong to class carbohydrates • Erythrose is found in erythrocytes (RBC) Dr Seemal Jelani Chem-261

  27. Determine the relationship • Find the relationship between the following • (a) and (c) • (a) and (d) • (b) and (c) • (b) and (d) They are non-superposable, but are not mirror images so they are Diastereoisomers. Dr Seemal Jelani Chem-261

  28. DIASTEREOISOMER Dr Seemal Jelani Chem-261 2-Methylcyclopentanol

  29. Diastereomers: • Stereoisomers that are not mirror images • Refers to the relationship among two or more objects Dr Seemal Jelani Chem-261

  30. Dr Seemal Jelani Chem-261

  31. O H H O O H H O cis- 1,2-Cyclopentanediol (a meso compound) H O O H O H H O trans- 1,2-Cyclopentanediol (a pair of enantiomers) H H H H diastereomers 1,2-Cyclopentanediol Dr Seemal Jelani Chem-261 H H H H

  32. Practice • Four stereoisomers of 1,2,3-butanetriol • Write IUPAC names and show the R and S configuration of each stereocenter • Identify enantiomers • Identify diasteromers Dr Seemal Jelani Chem-261

  33. Dr Seemal Jelani Chem-261

  34. MESO COMPOUNDS Dr Seemal Jelani Chem-261 2,3-Dihydroxybutanedioic acid (tartaric acid)

  35. Multiple sterocenters • Special symmetry leads to reduce number of stereoisomers than expected by the 2n Rule • Example: 2,3-Dihydroxybutanedioic acid • Commonly called Tartaric acid Dr Seemal Jelani Chem-261

  36. TA is a colorless, crystalline compound. • During the fermentation of grape juice, potassium bitartrate (one carboxyl group is present as a potassium salt, -COO-K+), deposits as a crust on the sides of wine casks Dr Seemal Jelani Chem-261

  37. This is collected and purified and sold commercially as a cream of tartar Dr Seemal Jelani Chem-261

  38. (c) (d) (a) (b) 1800 Dr Seemal Jelani Chem-261

  39. Carbon 2 and 3 are stereocenters 2n 2x2=4 stereoisomers or stereorepresentations (a) and (b) are • Non superposable mirror images • Therefore (a) and (b) are A pair of Enantiomer Dr Seemal Jelani Chem-261

  40. (c) and (d) are mirror images but they are superposable How? Imagine that you first rotate (d) by 1800 in the plane of the paper, cut and place it on (c) In doing so we found that (d) is superposable on (c) therefore we Dr Seemal Jelani Chem-261

  41. Say that (c) and (d) are not different molecules, they are the same molecules just oriented differently Because (c) and its mirror image are superposable so (c) is achiral Dr Seemal Jelani Chem-261

  42. Another way to determine that (c) is Achiral • We can see that it has plane of symmetry that bisect the molecule in such a way that the top half is the reflection of the bottom half • Thus even though ( c) has two sterocenters it is achiral Dr Seemal Jelani Chem-261

  43. conclusion • The stereoisomers of tartaric acid are represented ( c) or (d) is called MESO COMPOUND So meso compound is an achiral compound that contains two or more stereocenters Dr Seemal Jelani Chem-261

  44. Two chiral centers • 2n = 4, but only three stereoisomers exist Dr Seemal Jelani Chem-261

More Related