Chapter 28: Question 28.13 (page 1106)
Question: Convert each aldohexose to the indicated anomer using a Haworth projection
Short Answer
Answer
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Chapter 28: Question 28.13 (page 1106)
Question: Convert each aldohexose to the indicated anomer using a Haworth projection
Answer
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Question: Draw two possible epimers of D-erythrose. Name each of these compounds using Figure 28.4.
Identify the compounds A-D. A D-aldopentose A is oxidized with to an optically inactive aldaric acid. B. A undergoes the Kiliani-Fischer synthesis to yield C and D. C is oxidized to an optically active aldaric acid. D is oxidized to an optically inactive aldaric acid.
The following isomerization reaction, drawn using D-glucose as starting material, occurs with all aldohexoses in the presence of base. Draw a stepwise mechanism that illustrates how each compound is formed.

Question: Convert the ball-and-stick model to a Fischer projection.

Consider the following six compounds (A-F).

How are the two compounds in each pair related? Choose from enantiomers, epimers, diastereomers but not epimers, constitutional isomers, and identical compounds.
A and B
A and C
B and C
A and D
E and F
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