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- 1. A) Starting with the following line angle structure, convert the structure to a Fischer Projection. B) Determine the absolute configuration of the stereocenters as R or S. C) State whether the compound is chiral, achiral but not meso, achiral but meso. wwwwww H₂C H OH 1994. H CH3 OH #D) 12. Which of the following Newman Projections is the enantiomer to the molecule below H B) НО Н.С. HO H HO HC HO H Ф CH3 H Н CH₂ H CH₂ Hd
- Identify each pair as one of the following: (i) non-isomers, (ii) identical, (iii) configurational, (iv) conformational, (v) enantiomers, (vi) diastereomers. Please try to explain why if you can.Is cis-1,2-dibromocyclohexane a meso compound? In its planar structure, it has a line of symmetry but it has two chiral carbons. However, in its chair conformation, it does not look like it has a line of symmetry but it has two chiral carbons.An example of a chiral center is a carbon that bears 4 different groups, and therefore has no symmetry. Select ALL of the molecules that contain a chiral center. CI 요 Br 8 Br
- For the following molecule assign R or S to any chiral center if appropriate. Select the correct answer from the list below. cis CI trans OS this molecule is achiral so assigning R or S is not appropriate. RFor the following molecules, draw all possible stereoisomers using line-angle formulas with wedge/dash notation. Label the stereocenters as R or S. Indicate which ones are enantiomers and which ones are diastereomers. (Remember: there are 2 stereoisomers possible for a molecule with n chiral centers) (A) (B) (C) (1 chiral center) Br OH (2 chiral centers) CI OH CH3 (3 chiral centers)Iddentify the stereocenters on the given molecule.