Organic Chemistry, Books a la Carte Edition (9th Edition)
Organic Chemistry, Books a la Carte Edition (9th Edition)
9th Edition
ISBN: 9780134160382
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 5.10A, Problem 5.17P

Draw a Fischer projection for each compound. Remember that the cross represents an asymmetric carbon atom, and the carbon chain should be along the vertical, with the IUPAC numbering from top to bottom.

  1. a. (S)-propane-1,2-diol
  2. b. (R)-2-bromobutan 1-ol
  3. c. (S)-1,2-dibromobutane
  4. d. (R)-butan-2-ol

Chapter 5.10A, Problem 5.17P, Draw a Fischer projection for each compound. Remember that the cross represents an asymmetric carbon

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5. Draw the structure of (S)-1-bromo-1-chloropropane. Take care to indicate the three- dimensional stereochemistry properly. 6. How many chiral centers does the following compound contain? CH3 7. Label each chiral carbon in the molecule below as having R or S configuration. HO₂C H F. H3C H CH₂CH3
1. Draw the two conformations of trans-1-bromo-3-methylcyclohexane using both the Newman projection and the chair drawing. Calculate the energies of each. What ratio of the two conformers will be present at equilibrium? 2. Draw a structure of a chiral alcohol.
Glucose is a simple sugar with five substituents bonded to a sixmembered ring.a.Using a chair representation, draw the most stable arrangement of these substituents on the six-membered ring. b.Convert this representation to one that uses a hexagon with wedges and dashed wedges. c.Draw a constitutional isomer of glucose. d.Draw a stereoisomer that has an axial OH group on one carbon.
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