i need the answer quickly How can 2-(3-oxobutyl)cyclohexanone be prepared from cyclohexanone inthree steps? Select the appropriate reagents A, B and C for each step of thesynthesis in the correct order.ABзя0:46:52ABCPyrrolidine with trace acidDilute HCI with waterAcetic acidPropyl bromideMethyl vinyl ketoneFormaldehydeSodium hypochloriteMg in etherEthyl bromide

In Micheal's addition reaction a nucleophilic addition reaction takes place at the carbon-carbon…

Answered: How can 2-(3-oxobutyl)cyclohexanone be…

How can 2-(3-oxobutyl)cyclohexanone be prepared from cyclohexanone in three steps? Select the appropriate reagents A, B and C for each step of the synthesis in the correct order. 0:46:52

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Concept explainers

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.

Question

i need the answer quickly

How can 2-(3-oxobutyl)cyclohexanone be prepared from cyclohexanone in
three steps? Select the appropriate reagents A, B and C for each step of the
synthesis in the correct order.
A
B
зя
0:46:52
A
B
C
Pyrrolidine with trace acid
Dilute HCI with water
Acetic acid
Propyl bromide
Methyl vinyl ketone
Formaldehyde
Sodium hypochlorite
Mg in ether
Ethyl bromide

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Step 1: Micheal's addition reaction

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