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Chapter 23: Q10P (page 764)

What product would you expect to obtain from the base treatment of 1,6-cyclo-decanedione?

Short Answer

Expert verified

It gives seven-member ring fused with the five-member ring.

Step by step solution

01

Intramolecular aldol condensation:


02

Removal of a water molecule on heating and formation of double bond:

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Most popular questions from this chapter

How would you prepare the following compound using a Robinson annulation reaction between a饾泝-diketone and an饾泜,饾泝 -unsaturated ketone? Draw the structures of both reactants and the intermediate Michael addition product

Which of the following compounds can probably be prepared by a mixed aldol reaction? Show the reactants you would use in each case.

Show the products you would expect to obtain by Claisen condensation of the following esters:(a) CH3CHCH2CO2Et (b) Ethyl phenylacetate (c) Ethyl cyclohexyl acetate

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The bicyclic ketone shown below does not undergo aldol self-condensation even though it has two hydrogen atoms. Explain.
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