Chapter 23: Q14 P (page 1085)
Short Answer
- From pyruvate:
- From oxaloacetate
Chapter 23: Q14 P (page 1085)
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Instead of adding to the 4a position and protonating N-5, the thiolate ion could have added to the 10a position and protonated N-1. (The numbering system is on page 1071.) Why is addition to the 4a position favored? (Hint:Which nitrogen is a stronger base?)
Explain why the hydrogens of the C-8 methyl group are more acidic than those of the C-7 methyl group.
Question: Do all triacylglycerols have the same number of asymmetric centers?
How many conjugated double bonds are there in
a. FAD?
b. FADH2
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