Chapter 31: Question 31.6 (page 1239)
Draw the structure of a lecithin containing oleic acid and palmitic acid as the fatty acid side chains.
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Chapter 31: Question 31.6 (page 1239)
Draw the structure of a lecithin containing oleic acid and palmitic acid as the fatty acid side chains.
Answer

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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?
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.

What is the structure of an optically inactive triacylglycerol that yields two moles of oleic acid and one mole of palmitic acid when hydrolyzed in aqueous acid?
(a) Draw a skeletal structure of the anabolic steroid 4-androstene-3, 17-dione, also called 鈥渁ndro,鈥 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.
The main fatty acid component of the triacylglycerols in coconut oil is lauric acid, . Explain why coconut oil is a liquid at room temperature even though it contains a large fraction of this saturated fatty acid.
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