Chapter 22: 58E (page 752)
How would you synthesize the following compounds from cyclohexanone?
More than one step may be required.
Short Answer
a)
b)
c)
d)
e)
f)
Chapter 22: 58E (page 752)
How would you synthesize the following compounds from cyclohexanone?
More than one step may be required.
a)
b)
c)
d)
e)
f)
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How would you prepare the following ketones using an acetoacetic ester synthesis?
The two optically beta-keto acids below were decarboxylated using the conditions typically used for the acetoacetate synthesis. Will the ketone products also be optically active? Provide the complete mechanism to explain your answer.
Using curved arrows, propose a mechanism for the following reaction, one of the steps in the metabolism of the amino acid alanine.
Which of the following substances would undergo the haloform reaction?
(a)CH3COCH3 (b) Acetophenone (c) CH3CH2CHO
(d)CH3CO2H (e)
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