Friedel-Crafts Reactions and Mechanisms

Friedel-Crafts Reactions and Mechanisms

Assessment

Interactive Video

Science

8th Grade

Hard

Created by

Wayground Resource Sheets

FREE Resource

8 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the basic building block used to create polystyrene?

Toluene

Styrene

Cumene

Phenol

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

From what natural resource is benzene primarily obtained?

Natural gas

Crude oil

Biomass

Coal

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What type of chemical reaction occurs when an alkene reacts with bromine?

Electrophilic substitution

Electrophilic addition

Dehydrogenation

Nitration

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the reaction where benzene reacts with bromine, what is the main purpose of adding a catalyst like FeBr3?

To make benzene more reactive

To make bromine a stronger electron-seeking molecule

To remove hydrogen from the benzene ring

To slow down the reaction

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the positively charged ion that acts as an electrophile in the nitration of benzene?

Sulfate ion (SO4^2-)

Nitronium ion (NO2^+)

Hydroxyl ion (OH^-)

Hydrogen ion (H^+)

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the nitration of benzene, what is the role of sulfuric acid?

It is a reactant that gets used up in the process.

It helps dissolve the other chemicals.

It speeds up the reaction without being consumed.

It is the main product formed.

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

When 1-chloro-2-methylpropane reacts with benzene in a Friedel-Crafts alkylation, which product is mainly formed due to a rearrangement?

2-methylpropylbenzene

tert-butylbenzene

Isopropylbenzene

Chlorobenzene

8.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a key difference in the intermediate formed during Friedel-Crafts acylation compared to alkylation?

Acylation forms a carbocation that is less stable than in alkylation.

Acylation forms an acylium ion that is stabilized by resonance and does not rearrange.

Alkylation forms an acylium ion, while acylation forms a carbocation.

Acylation reactions do not require a Lewis acid catalyst.