Podcast
Questions and Answers
What is the product formed when 1,3-dibromopropane is treated with sodium or zinc?
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?
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?
What is the most satisfactory catalyst for the conversion of phenol to cyclohexanol?
- $Na/C2H5OH H2SO4$
- $Na/C2H5OH H2SO4$
- $Ni / 200° 3 H2$ (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?
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?
What happens to dihalogen derivatives of paraffins in which the two halogen atoms are further apart than the 1,5-positions?
What happens to dihalogen derivatives of paraffins in which the two halogen atoms are further apart than the 1,5-positions?
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.