Chapter 31: Q18P. (page 1256)
Convert each ball-and-stick model to a skeletal structure that clearly shows the stereochemistry at the ring fusion of these decalin derivatives.
A.
B.
Short Answer
A.
B.
Chapter 31: Q18P. (page 1256)
Convert each ball-and-stick model to a skeletal structure that clearly shows the stereochemistry at the ring fusion of these decalin derivatives.
A.
B.
A.
B.
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Get started for free(a) Draw a skeletal structure of the anabolic steroid 4-androstene-3, 17-dione, also called โandro,โ from the following description. Andro contains the tetracyclic steroid with carbonyl groups at C3 and C17, a double bond between C4 and C5, and methyl groups bonded to C10 and C13.
(b) Add wedges and dashed wedges for all stereogenic centers with the following information: the configuration at C10 is R, the configuration at C13 is S, and all substituents at ring fusions are trans to each other.
Why are phospholipids, but not triacylglycerols, found in cell membranes?
How would you expect the melting point of eicosapentaenoic acid to compare with the melting points of the fatty acids listed in Table 31.2?
A difficult problem in the synthesis of PGFis the introduction of the OH group at C15 in the desired configuration.
A well known synthesis of PGFinvolves reaction of A with (a metal hydride reagent similar in reactivity to, to form two isomeric products, B and C. Draw their structures and indicate their stereochemical relationship.
Suggest a reagent to convert A to the single stereoisomer X.
Draw three-dimensional structures for each alcohol. Label the OH groups as occupying axial or equatorial positions.
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b.
c.
d.
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