Exam 30: Lipids

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What happens to the melting point in fatty acids as the unsaturation increases?

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What is the correct classification of the following compound? CH3(CH2)15COOH

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How many isoprene units are contained in the following molecule? How many isoprene units are contained in the following molecule?

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Provide a definition of the term lipid.

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Which of the following classes of molecules is not a nonhydrolyzable lipid?

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What is the name of the reaction of triglycerides with a base?

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Which of the following compounds is a steroid? Which of the following compounds is a steroid?

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Which of the following are complex lipids?

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Which of the following fatty acids is not present in natural fats and oils?

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Sphingomyelins are a major component of the myelin sheath. Damage to the myelin sheath results in such diseases as multiple sclerosis. Which compound below corresponds to a sphingomyelin? Sphingomyelins are a major component of the myelin sheath. Damage to the myelin sheath results in such diseases as multiple sclerosis. Which compound below corresponds to a sphingomyelin?

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Eicosanoids are derived from what compound?

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Which of the following compounds is not a lipid? Which of the following compounds is not a lipid?

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Which of the following is not one of the three main categories of hydrolyzable lipids?

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What is the result of the oxidation of arachidonic acid with O2 by cyclooxygenase?

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Which of the following fatty acids has the highest melting point?

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Which structure represents the lowest energy conformation of a trans-decalin? Which structure represents the lowest energy conformation of a trans-decalin?

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Which of the following sequences shows a reasonable series of 1,2-rearrangements as might be found in the biosynthesis of a steroid? Which of the following sequences shows a reasonable series of 1,2-rearrangements as might be found in the biosynthesis of a steroid?

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Which of the following fatty acids has the lowest melting point?

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What chemical process causes an oil (such as soybean oil) to become rancid?

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The stereoselective introduction of the C15 OH group on the side chain of prostaglandins has presented a challenge for synthetic chemists. Recently, Mulzer and co-workers demonstrated a new route in which the side chain is synthesized independently and then attached to the bicyclic counterpart. What is the appropriate sequence of reagents for the following synthesis? The stereoselective introduction of the C15 OH group on the <font face=symbol></font> side chain of prostaglandins has presented a challenge for synthetic chemists. Recently, Mulzer and co-workers demonstrated a new route in which the <font face=symbol></font> side chain is synthesized independently and then attached to the bicyclic counterpart. What is the appropriate sequence of reagents for the following synthesis?

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