Chapter 31: Question 31.17 (page 1256)
Locate the isoprene units in each compound.
a.
b.
Short Answer
Answer
a.
b.
Chapter 31: Question 31.17 (page 1256)
Locate the isoprene units in each compound.
a.
b.
Answer
a.
b.
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Get started for freeDraw all possible constitutional isomers of a triacylglycerol formed from one mole each of palmitic, oleic, and linoleic acids. Locate the tetrahedral stereogenic centers in each constitutional isomer.
One component of lanolin, the wax that coats sheep’s wool, is derived from cholesterol and stearic acid. Draw its structure, including the correct stereochemistry of all stereogenic centers.
Question: An isoprene unit can be thought of as having a head and a tail. The “head” of the isoprene unit is located at the end of the chain nearest the branch point, and the “tail” is located at the end of the carbon chain farthest from the branch point. Most isoprene units are connected together in a “head-to-tail” fashion, as illustrated. For both lycopene (Problem 31.26), and squalene (Figure 31.9), decide which isoprene units are connected in a head-to-tail fashion and which are not.
Locate the isoprene units in each compound.
a.
b.
c.
d.
Draw the products formed when triacylglycerol A is treated with each reagent. Rank compounds A, B and C in order of increasing melting point.
a.,
b. (excess),
c.(1 equiv),
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