Intro to Electrophilic Aromatic Substitution: Crash Course Organic Chemistry

Intro to Electrophilic Aromatic Substitution: Crash Course Organic Chemistry

Assessment

Interactive Video

Chemistry, Science

11th Grade - University

Hard

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Quizizz Content

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The video explores the chemistry of benzene, focusing on electrophilic aromatic substitution reactions. It compares alkene addition with benzene reactions, highlighting the need for catalysts. The video covers nitration, sulfonation, and Friedel-Crafts reactions, explaining their mechanisms and industrial applications. Safety considerations for handling chemicals like nitrobenzene are also discussed.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary source of benzene used in the chemical industry?

Natural gas

Crude oil

Coal

Wood

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why does benzene require a catalyst for electrophilic aromatic substitution?

Benzene lacks true double bonds

Benzene has a high boiling point

Benzene is too reactive on its own

Benzene is a strong nucleophile

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What role does ferric bromide play in the bromination of benzene?

It provides a source of bromine

It acts as a Lewis acid catalyst

It acts as a nucleophile

It stabilizes the benzene ring

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which compound is used to nitrate benzene?

Sulfuric acid and nitric acid

Hydrochloric acid and nitric acid

Nitric acid and acetic acid

Sulfuric acid and hydrochloric acid

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the electrophile in the nitration of benzene?

Sulfur trioxide (SO3)

Chlorine ion (Cl-)

Hydronium ion (H3O+)

Nitronium ion (NO2+)

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main product of Friedel-Crafts alkylation using isopropyl chloride?

Phenol

Benzaldehyde

Cumene

Tert-butylbenzene

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a potential issue with Friedel-Crafts alkylation reactions?

Formation of unstable carbocations

Excessive production of by-products

Rearrangement to more stable carbocations

Inability to form carbon-carbon bonds

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