Organic Chemistry

(Dana P.) #1

030 CHAPTER 26 Lipids



  1. Nutmeg contains a simple, fully saturated triacylglycerol with a molecular weight of 722. Draw its structure.

  2. Give the product that would be obtained from the reaction of cholesterol with each of the following reagents: (Hint:Because of
    steric hindrance from the angular methyl groups, the is more susceptible to attack by reagents than the .)
    a.
    b. in THF, followed by
    c. Pd C
    d.
    e. peroxyacetic acid
    f. the product of part

  3. Dr. Cole S. Terol synthesized the following samples of mevalonic acid and fed them to a group of lemon trees:


Which carbons in citronellal, which is isolated from lemon oil, will be labeled in trees that were fed the following?
a. sample A b. sample B c. sample C


  1. An optically active monoterpene (compound A) with molecular formula undergoes catalytic hydrogenation to form an
    optically inactive compound with molecular formula (compound B). When compound B is heated with acid, followed by
    reaction with and workup under reducing conditions one of the products obtained is 4-methylcyclohexanone. Give
    possible structures for compound A.

  2. If junipers were allowed to grow in a medium containing acetate in which the methyl carbon was labeled with which carbons
    in would be labeled?

  3. a. Propose a mechanism for the following reaction:


b. To what class of terpene does the starting material belong? Mark off the isoprene units in the starting material.


  1. 5-Androstene-3,17-dione is isomerized to 4-androstene-3,17-dione by hydroxide ion. Propose a mechanism for this reaction.


5-androstene-3,17-dione

H 3 C

H 3 C

O

HO−
H 2 O

O

4-androstene-3,17-dione

H 3 C

H 3 C

O

O

CH 3

CH 3

CH 3 CH 3

H 3 C

H 3 C

HO

H+

CH 3

CH 3 H 3 C CH 3

H 3 C CH 3

CH + H^3 O+
3

H 3 C CH 3

CH 3

a-terpineol

14 C,

O 3 , 1 Zn, H 2 O 2 ,

C 10 H 20 O

C 10 H 18 O

CH 2 CO−

CH 3 CCH 2 CH 2 OH

OH

O
sample A

CH 2 CO−

CH 3 CCH 2 CH 2 OH

OH

O
sample B

CH 2 CO−

CH 3 CCH 2 CH 2 OH

OH

O
sample C

14

14 14

cholesterol

H 3 C H

H H

H 3 C

HO

e+CH 3 O-

Br 2 +H 2 O

H 2 , >

BH 3 H 2 O 2 +HO-

H 2 O, H+

a-face b-face
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