Chapter 12: Q62E (page 354)
How would you prepare the following substances from 2-cyclohexenone? More than one step may be needed.
a.

b.

c.

d.

Short Answer
a.

b.

c.

d.

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Chapter 12: Q62E (page 354)
How would you prepare the following substances from 2-cyclohexenone? More than one step may be needed.
a.

b.

c.

d.

a.

b.

c.

d.

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Predict the products for the reactions in Problem 8-26 if each were run in DMSO with water. Show the complete mechanism including appropriate regiochemistry and stereochemistry.
Carvone is an unsaturated ketone responsible for the odour of spearmint. If carvone hasin its mass spectrum and contains three double bonds and one ring, what is its molecular formula?
Phenol,, is a stronger acid than methanol, , even though both contain an OH bond. Draw the structures of the anions resulting from loss of from phenol and methanol, and use resonance structures to explain the difference in acidity.

Using curved arrows to indicate the electron flow in each step, show how the base-catalyzed retro-aldol reaction of 4-hydroxy-4-methyl-2-pentanone takes place to yield 2 equivalents of acetone.

Draw structures corresponding to the following IUPAC names:
a)cis-1,2-Cyclohexanedicarboxylic acid
b) Hepatanedioic acid
c) 2-Hexen-4-ynoic acid
d) 4-Ethyl-2-propyloctanoic acid
e) 3-chlorophthalic acid
f) Triphenylacetic acid
g) 2-Cyclobutenecarbonitrile
h) m-Benzoylbenzonitrile
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