a) Acetoacetic ester can be prepared from Claisen self-condensation reaction of ethyl acetate. You are given ethanol as the only starting material. Using all the available reagents in the organic chemistry lab, illustrate how acetoacetic ester can be synthesised. Show all reagents and structures for all the intermediates. b) Provide the synthons and synthetic equivalents for the following compounds. i) Synthons: Synthetic equivalents: ii) Synthons: OH Synthetic equivalents:
a) Acetoacetic ester can be prepared from Claisen self-condensation reaction of ethyl acetate. You are given ethanol as the only starting material. Using all the available reagents in the organic chemistry lab, illustrate how acetoacetic ester can be synthesised. Show all reagents and structures for all the intermediates. b) Provide the synthons and synthetic equivalents for the following compounds. i) Synthons: Synthetic equivalents: ii) Synthons: OH Synthetic equivalents:
Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Solve (a) and (b)
![a) Acetoacetic ester can be prepared from Claisen self-condensation reaction of
ethyl acetate. You are given ethanol as the only starting material. Using all the
available reagents in the organic chemistry lab, illustrate how acetoacetic ester can
be synthesised. Show all reagents and structures for all the intermediates.
b) Provide the synthons and synthetic equivalents for the following compounds.
i)
Synthons:
Synthetic equivalents:
ii)
Synthons:
OH
Synthetic equivalents:](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F474f3f02-112a-4977-a49d-b18399a58460%2F1dd6e5cc-414d-44b2-8bf1-959053e72696%2Fvqvta3l_processed.png&w=3840&q=75)
Transcribed Image Text:a) Acetoacetic ester can be prepared from Claisen self-condensation reaction of
ethyl acetate. You are given ethanol as the only starting material. Using all the
available reagents in the organic chemistry lab, illustrate how acetoacetic ester can
be synthesised. Show all reagents and structures for all the intermediates.
b) Provide the synthons and synthetic equivalents for the following compounds.
i)
Synthons:
Synthetic equivalents:
ii)
Synthons:
OH
Synthetic equivalents:
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