
Friedel Crafts Reactions and Directing Effects

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Chemistry
•
11th - 12th Grade
•
Hard

Jackson Turner
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9 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the main chemical process discussed for generating the compound from benzene?
Electrophilic aromatic substitution
Radical substitution
Elimination reaction
Nucleophilic substitution
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which reaction is used to attach an alkyl group to a benzene ring?
Nitration
Friedel Crafts alkylation
Friedel Crafts acylation
Sulfonation
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the role of the Friedel Crafts alkylation in this process?
To add an alkyl group to the benzene ring
To oxidize the benzene ring
To change the benzene ring to a cyclohexane
To remove the nitro group
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What type of director is an alkyl group in electrophilic aromatic substitution?
Meta director
Ortho/para director
Para director only
Ortho director only
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is the spatial relationship between substituents important in this reaction?
It determines the reaction speed.
It affects the solubility of the compound.
It dictates the order of reactions to achieve the desired product.
It changes the color of the compound.
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the directing effect of a nitro group in electrophilic aromatic substitution?
Ortho director only
Para director only
Meta director
Ortho/para director
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What would happen if nitration was performed before alkylation?
The alkyl group would not attach to the benzene ring.
The nitro group would direct the alkyl group to the meta position.
The reaction would not proceed.
The nitro group would direct the alkyl group to the ortho position.
8.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which group is responsible for directing the nitro group to the ortho position?
Nitro group
Alkyl group
Carboxyl group
Hydroxyl group
9.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the final step to obtain the target molecule after the reactions?
Separating the ortho and para products
Heating the mixture
Performing a second nitration
Adding a catalyst
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