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Methods of Preparing Allicyclic Compounds Quiz

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Methods of Preparing Allicyclic Compounds Quiz

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Questions and Answers

What is the product formed when 1,3-dibromopropane is treated with sodium or zinc?

Cyclopropane (correct)

Cyclobutane

Cyclohexane

Cyclopentane

What is the product of the dry distillation of barium adipate?

Cyclohexanone

Cyclopentanone (correct)

Cycloheptanone

Cyclobutanone

What is the most satisfactory catalyst for the conversion of phenol to cyclohexanol?

$Na/C2H5OH H2SO4$

$Ni / 200° 3 H2$ (correct)

$Zn/Hg$

What is the product formed when alpha,w – dibromides condense with one molecule of malonic ester in the presence of two molecules of sodium ethoxide?

<p>Cycloalkane -1,1-dicarboxylic ester</p> Signup and view all the answers

What happens to dihalogen derivatives of paraffins in which the two halogen atoms are further apart than the 1,5-positions?

<p>Undergo the Wurtz reaction</p> Signup and view all the answers

Study Notes

Reactions and Products

1,3-Dibromopropane reacts with sodium or zinc to form cyclopropane.
Dry distillation of barium adipate produces cyclohexane.
The most effective catalyst for converting phenol to cyclohexanol is zinc chloride.
Alpha,w-dibromides react with malonic ester in the presence of sodium ethoxide to form cycloalkanecarboxylic acids.
Dihalogen derivatives of paraffins, where the two halogen atoms are farther apart than the 1,5-positions, undergo dehydrohalogenation to form alkenes.

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Description

Test your knowledge about the methods of preparing allicyclic compounds with this quiz. Learn about Freund reaction and other important processes for synthesizing cycloparaffins.