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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

Which of the following compounds are aldol condensation products? What is the aldehyde or ketone precursor of each?

(a) 2-Hydroxy-2-methylpentanal (b) 5-Ethyl-4-methyl-4-hepten-3-one

Predict the product(s) and provide the mechanism for each reaction below.

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

Based on your answers to Problem 23-27, predict the dehydration product for each reaction and provide the mechanism.

How would you prepare the following compounds from cyclohexanone?
See all solutions

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