When CH₃Cl and AlCl₃ are used in Friedel-Crafts reaction,
the electrophile is
(a) Cl⁺ (b) AlCl₄⁻
(c) CH₃⁺ (d) AlCl₂⁺
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Explanation:
the electrophile is Cl⁺ in the given reaction
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When CH₃Cl and AlCl₃ are used in Friedel-Crafts reaction, the electrophile is Cl⁺.
Explanation:
Friedel-Crafts Alkylation
- It is an organic coupling reaction which involves an electrophilic in aromatic substitutions. The reactions involves in both acylation and alkylation.
- An alkyl group will replace an aromatic proton. It is done by an electrophile which attacks the aromatic ring using carbocation.
- Alkyl benzene is the method generated from Friedel-Crafts alkylation reaction as the reactants as alkyl halides.
- or are employed as Lewis acid catalyst for this reaction to form carbocation and remove halides.
- In chlorine atom, accept the chloride ion and pair of electron from the S-Cl bond, so covalent bond cannot be formed. It is either nucleophile or electrophile.
To learn more;
- https://brainly.in/question/5913150
- https://brainly.in/question/8882256
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