Separating Components of a Mixture by Extraction

Separating Components of a Mixture by Extraction

Assessment

Interactive Video

Chemistry, Science

11th Grade - University

Hard

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The video tutorial explains the process of extraction, a technique used to separate components of a mixture based on their physical and chemical properties. It begins with a simple example of separating sodium chloride and cholesterol using their differing solubilities. The tutorial then progresses to a more complex example involving 4-chloroaniline, benzoic acid, and dibromobenzene, demonstrating the use of acid-base reactions to achieve separation. The video concludes by highlighting the importance of extraction in organic chemistry labs and encourages familiarity with the separatory funnel.

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7 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What physical property is used to separate sodium chloride and cholesterol in the example provided?

Solubility

Magnetism

Boiling point

Density

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the complex example, which compound reacts with hydrochloric acid due to its basic nature?

Benzoic acid

Sodium chloride

1,4-dibromobenzene

4-chloroaniline

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the role of sodium bicarbonate in the separation process?

To protonate aniline

To evaporate ether

To react with benzoic acid

To dissolve 1,4-dibromobenzene

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How is dibromobenzene recovered from the ether solution?

By adding a strong acid

By adding sodium hydroxide

By evaporating the ether

By using a vacuum pump

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the purpose of using a Buchner funnel in the recovery process?

To mix the solutions

To measure the pH

To evaporate solvents

To filter and dry the precipitate

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which compound requires a strong base for deprotonation during recovery?

Cholesterol

Benzoic acid

4-chloroaniline

1,4-dibromobenzene

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the final pH range indicating the completion of the deprotonation of the aniline salt?

Around 2

Around 7

Around 5

Around 11 or 12