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Friedel-Craft’s reaction using MeCl and anhydrous AlCl3 will take place most efficiently with
  • a)
     Benzene
  • b)
    Nitrobenzene
  • c)
    Acetophenone
  • d)
    Toluene
Correct answer is option 'D'. Can you explain this answer?
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Explanation:

Friedel-Craft's acylation is a type of electrophilic aromatic substitution reaction in which an acyl group is introduced onto an aromatic ring. In this reaction, anhydrous aluminum chloride (AlCl3) acts as a Lewis acid catalyst, facilitating the formation of the acylium ion, which then reacts with the aromatic compound.

Efficiency of Friedel-Craft's reaction:

The efficiency of the Friedel-Craft's reaction using MeCl (methyl chloride) and anhydrous AlCl3 depends on the reactivity of the aromatic compound. Toluene is more reactive towards Friedel-Craft's acylation compared to benzene, nitrobenzene, or acetophenone due to its higher electron density.

Reason for choosing toluene:

- Toluene has a methyl group which is an activating group, increasing the electron density on the aromatic ring.
- The increased electron density makes toluene more susceptible to electrophilic attack, leading to a more efficient Friedel-Craft's acylation reaction.
- Benzene, nitrobenzene, and acetophenone are less reactive due to the presence of deactivating groups or lack of activating groups.

Therefore, the Friedel-Craft's reaction using MeCl and anhydrous AlCl3 will take place most efficiently with toluene among the given options.
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Friedel-Craft’s reaction using MeCl and anhydrous AlCl3 will take place most efficiently witha)Benzeneb)Nitrobenzenec)Acetophenoned)TolueneCorrect answer is option 'D'. Can you explain this answer?
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