Methods of Preparing Allicyclic Compounds Quiz

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5 Questions

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

Cyclopropane

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

Cyclopentanone

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

$Ni / 200° 3 H2$

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?

Cycloalkane -1,1-dicarboxylic ester

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

Undergo the Wurtz reaction

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.

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

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