Chapter 28: Question 28.8 (page 1106)
Question: Draw two possible epimers of D-erythrose. Name each of these compounds using Figure 28.4.
Short Answer
Answer
D-threose
L-threose
Chapter 28: Question 28.8 (page 1106)
Question: Draw two possible epimers of D-erythrose. Name each of these compounds using Figure 28.4.
Answer
D-threose
L-threose
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Get started for freeA D-aldopentose A is reduced to an optically active alditol. Upon Kiliani-Fischer synthesis, A is converted to two D-aldohexoses, B and C. B is oxidized to an optically inactive aldaric acid. C is oxidized to an optically active aldaric acid. What are the structures of A-C?
Question:How many different aldoheptoses are there? How many are d-sugars? Draw all d-aldoheptoses having the Rconfiguration at C2 and C3.
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: Label each stereogenic center as RorS.
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