Home
Class 11
CHEMISTRY
Electrophilic aromatic substitution can ...

Electrophilic aromatic substitution can be seen in which of the following cases ?

A

B

C

D

Text Solution

AI Generated Solution

The correct Answer is:
To determine in which cases electrophilic aromatic substitution occurs, we will analyze each of the provided options step by step. ### Step 1: Understanding Electrophilic Aromatic Substitution Electrophilic aromatic substitution (EAS) is a reaction where an electrophile replaces a hydrogen atom on an aromatic ring. This type of reaction typically requires the presence of an electrophile and a catalyst, often a Lewis acid. ### Step 2: Analyzing the Options 1. **Option A**: Friedel-Crafts Alkylation - In this reaction, a benzene ring reacts with an alkyl halide in the presence of a Lewis acid (like AlCl₃). The alkyl group replaces a hydrogen atom on the benzene ring, forming a new alkyl-substituted aromatic compound. - **Conclusion**: This is an example of electrophilic aromatic substitution. 2. **Option B**: Friedel-Crafts Acylation - Similar to alkylation, this reaction involves the acylation of a benzene ring using an acyl halide and a Lewis acid. The acyl group replaces a hydrogen atom on the aromatic ring. - **Conclusion**: This is also an example of electrophilic aromatic substitution. 3. **Option C**: Bromination of Aromatic Compounds - In this case, an aromatic compound reacts with bromine (Br₂) in the presence of a halogen carrier (like FeBr₃). The bromine acts as an electrophile and substitutes a hydrogen atom on the aromatic ring. - **Conclusion**: This is another example of electrophilic aromatic substitution. 4. **Option D**: Aliphatic Halogenation - This reaction involves the substitution of hydrogen in an aliphatic compound (not aromatic) with bromine in the presence of light. This is a free radical mechanism and does not involve an aromatic ring. - **Conclusion**: This is not an example of electrophilic aromatic substitution. ### Final Conclusion Electrophilic aromatic substitution can be observed in **Options A, B, and C**. Option D does not involve aromatic compounds and is therefore excluded. ### Summary of the Solution - **Options A, B, and C** are examples of electrophilic aromatic substitution. - **Option D** is not an example of electrophilic aromatic substitution.
Doubtnut Promotions Banner Mobile Dark
|

Topper's Solved these Questions

  • ORGANIC REACTION MECHANISMS - II

    RESONANCE ENGLISH|Exercise Exercise-2 Part-4|5 Videos
  • ORGANIC REACTION MECHANISMS - II

    RESONANCE ENGLISH|Exercise Exercise-3 Part-1|20 Videos
  • ORGANIC REACTION MECHANISMS - II

    RESONANCE ENGLISH|Exercise Exercise-2 Part-2|8 Videos
  • MOLE CONCEPT

    RESONANCE ENGLISH|Exercise ORGANIC CHEMISTRY(BASIC CONCEPTS)|27 Videos
  • ORGANIC REACTION MECHANISMS-IV

    RESONANCE ENGLISH|Exercise APSP PART-3|22 Videos

Similar Questions

Explore conceptually related problems

Electrophilic aromatic substitution is difficult in

Identify the position where electrophillic aromatic substitution (EAS) is most faourable .

Knowledge Check

  • above reaction is an example of Nucleophilic aromatic substitution. Which of the following halide (-X) is most readily replaced.

    A
    `_F`
    B
    `-Cl`
    C
    `-Br`
    D
    `-I`
  • The electrophilic aromatic substitution proceeds through a :

    A
    free radical
    B
    sigma complex
    C
    benzyne
    D
    carbene
  • Halogens are deactivating yet ortho,para directing in electrophilic aromatic substitution. Which statements do not explain this ?

    A
    A combination of inductive electron withdrawal and resonance electron release.
    B
    Inductive electron withdrawal with no resonance effect.
    C
    A combination of inductive electron release and resonance electron withdrawal.
    D
    A combination of inductive electron release and resonance electron release.
  • Similar Questions

    Explore conceptually related problems

    Sulfonation differs from most of electrophilic aromatic substitution reactions with the fact that the reaction-

    In which of the following , replum can be seen ?

    Althrough chlorine is an electron withdrawing group, yet it is ortho-para-directing in electrophilic aromatic substitution reactions. Explain why it is so ?

    Reimer-Tiemann reaction introduces an aldehyde group on to the aromatic ring of phenol, ortho to the hydroxyl group. This reacrtion involves electrophilic aromatic subsititution. It is a general method for the synthesis of subsituted salicyladehydes as depiced below: The electrophile in this reaction is:

    In which of the following compound electrophilic aromatic substitution take place in phenyl ring present in left hand side ?