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Q 103

Page 1256

Consider separate 1.0-L samples of O2(g) and He(g), both at 25oC and the same pressure. Compare the change in momentum per impact and the number of impacts per second in the two samples.

Q.26.

Page 1231

Question: Locate the isoprene units in each compound.

Q.29.

Page 1231

Question: An isoprene unit can be thought of as having a head and a tail. The 鈥渉ead鈥 of the isoprene unit is located at the end of the chain nearest the branch point, and the 鈥渢ail鈥 is located at the end of the carbon chain farthest from the branch point. Most isoprene units are connected together in a 鈥渉ead-to-tail鈥 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.

Q.30.

Page 1231

Question: Draw a stepwise mechanism for the conversion of neryl diphosphate to -pinene, -pineneis a component of pine oil and rosemary oil.

Q 31.10

Page 1246

Locate the isoprene units in each compound.

a.

b.

c.

d.

Question 31.10

Page 1246

Locate the isoprene units in each compound.

a.

b.

c.

d.

Question 31.15

Page 1253

Draw the enantiomer and any two diastereomers of cholesterol. Does the OH group of cholesterol occupy an axial or equatorial position?

Question 31.16

Page 1253

Treatment of cholesterol with mCPBA results in formation of a single epoxide A, with the stereochemistry drawn. Why isn鈥檛 the isomeric epoxide B formed to any extent?

Question 31.3

Page 1237

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.H2O,H+

b. H2(excess), Pd.CB

c.H2(1 equiv), Pd.CC

Question 31.38

Page 1256

Draw the products formed when cholesterol is treated with each reagent. Indicate the stereochemistry around any stereogenic centers in the product.

  1. CH3COCl
  2. H2,Pd-C
  3. PCC
  4. oleicacid,H+
  5. [1]BH3THF;[2]H2O2,-OH

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