Header image- Friedel-Crafts alkylation quiz

Friedel-Crafts alkylation quiz

Answer all the questions below then hit the check answer button and scroll down to get your score.

1. What type of mechanism is involved in a Friedel-Crafts alkylation reaction?

Nucleophilic substitution


2. What type of reagent is AlCl3 in a Friedel-Crafts alkylation reaction?




3. Which of the following molecules will fail to undergo a Friedel-Crafts alkylation reaction?




4. During a Friedel-Crafts alkylation reaction the halogen atom present on the halogenalkane donates a lone pair of electrons to the Lewis acid and is therefore acting as a base.

Image explains what an activating group when attached to an aromatic ring.

5. Which of the following groups will activate a benzene ring towards further electrophilic substitution?



A methyl group (-CH3)

6. A Lewis acid is an electron pair while a Lewis base is an electron pair .

7. Which type of carbocation is the most stable when formed during a Friedel-Crafts alkylation reaction?

Primary
Methyl

8. One reason why aryl halides do not undergo a Friedel-Crafts alkylation reaction is that the C-X bond is too .

9. What happens to the delocalised pi electron system in a benzene ring during electrophilic substitution reactions?




Cartoon style to show limitation of Friedel-Crafts alkylation reactions due to polyalkylation.

10. What intermediate is formed during the reaction between 2-chloropropane and AlCl3?




11. Which of the following is not a common Lewis acid used in a Friedel-Crafts alkylation reaction?




12. One of the major limitations of Friedel-Crafts alkylation reactions is that they often under reactions, this is where alkyl groups are added onto an aromatic ring.

13. Which of the following species is likely to remove a proton (H+) in a Friedel-Crafts alkylation reaction?




14. Which of the following can act as a Lewis base in a Friedel-Crafts alkylation reaction?