Benzene to ethylbenzene
1 step: Friedel-Crafts alkylation
BenzeneC₆H₆Arene - Step 1
CH₃CH₂Cl, anhydrous AlCl₃
EthylbenzeneC₆H₅CH₂CH₃Arene
Exam answer
- Step 1: Benzene to ethylbenzene: CH₃CH₂Cl, anhydrous AlCl₃.
Alternative routes (1)
- Benzene → Acetophenone → Ethylbenzene
- Benzene to acetophenone: CH₃COCl, anhydrous AlCl₃.
- Acetophenone to ethylbenzene: Zn-Hg, conc. HCl.
Reagent and reason, step by step
- Step 1: Benzene to ethylbenzene: CH₃CH₂Cl, anhydrous AlCl₃ Friedel-Crafts alkylation with a primary halide.
Benzene to ethylbenzene: quick answers
How many steps does it take to convert benzene to ethylbenzene?
1 step: Benzene, then ethylbenzene.
Which named reaction is used to convert benzene to ethylbenzene?
Friedel-Crafts alkylation. Benzene reacts with an alkyl halide in the presence of anhydrous AlCl3 to give an alkylbenzene.
What is the reagent for step 1 of benzene to ethylbenzene?
Benzene to ethylbenzene: CH₃CH₂Cl, anhydrous AlCl₃. Friedel-Crafts alkylation with a primary halide.