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    • https://espanol.libretexts.org/Quimica/Libro%3A_Qu%C3%ADmica_Org%C3%A1nica_con_%C3%A9nfasis_Biol%C3%B3gico_(Soderberg)/15%3A_Reacciones_electrofilicas/15.06%3A_Paralelo_sint%C3%A9tico_-_sustituci%C3%B3n_electrof%C3%ADlica_arom%C3%A1tica_en_el_laboratorio
      Because of the low reactivity of the aromatic π bond nucleophile, however, the acyl chloride electrophile in a Friedel-Crafts acylation must be further activated with a Lewis acid reagent such as alum...Because of the low reactivity of the aromatic π bond nucleophile, however, the acyl chloride electrophile in a Friedel-Crafts acylation must be further activated with a Lewis acid reagent such as aluminum trichloride, which again serves to polarize the carbon-chlorine bond and increase the electrophilicity of the acyl carbon.

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