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Isopropyl benzene can be obtained by :...

Isopropyl benzene can be obtained by :

A

B

C

D

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The correct Answer is:
To determine how isopropyl benzene can be obtained, we need to analyze the given options and the reactions involved. Isopropyl benzene, also known as cumene, can be synthesized through electrophilic substitution reactions involving benzene and appropriate alkyl halides. Here’s a step-by-step breakdown of the process: ### Step 1: Identify the reactants We start with benzene (C6H6) as the primary reactant. Benzene is known for its high electron density due to the delocalized π electrons, making it a good substrate for electrophilic substitution reactions. ### Step 2: Understand the electrophilic substitution mechanism In the presence of a Lewis acid catalyst like aluminum trichloride (AlCl3), an alkyl halide can react to form a carbocation, which acts as the electrophile. The general mechanism involves: 1. Formation of the electrophile from the alkyl halide. 2. Electrophilic attack on the benzene ring. 3. Restoration of aromaticity. ### Step 3: Analyze the options 1. **Option A**: Benzene + Propene in the presence of AlCl3 - Propene can form a secondary carbocation (isopropyl cation) when reacted with AlCl3, which can then react with benzene to form isopropyl benzene. 2. **Option B**: Benzene + Propyl chloride (C3H7Cl) in the presence of AlCl3 - Propyl chloride can also form a primary carbocation, but through a hydride shift, it can rearrange to a more stable secondary carbocation (isopropyl cation) that can react with benzene to form isopropyl benzene. 3. **Option C**: Benzene + Isopropyl chloride (C3H7Cl) in the presence of AlCl3 - Isopropyl chloride directly provides the isopropyl cation, which can react with benzene to yield isopropyl benzene. 4. **Option D**: Benzene + Ethyl phenyl ether - Ethyl phenyl ether does not generate a suitable electrophile for this reaction, as it does not lead to the formation of an isopropyl cation. ### Step 4: Conclusion Based on the analysis: - **Options A, B, and C** can yield isopropyl benzene. - **Option D** cannot yield isopropyl benzene. ### Final Answer: Isopropyl benzene can be obtained by options **A, B, and C**. ---
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HIMANSHU PANDEY-AROMATIC HYDROCARBONS-More Than One Correct (Q.1 To Q.25)
  1. Choose the compounds below that are antiaromatic :

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  2. Which of the following will undergo Friedel-Crafts alkylation reaction...

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  3. Which pairs are not required for a nucleophilic aromatic substitution ...

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  4. Halogens are deactivating yet ortho,para directing in electrophilic ...

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  5. Which of the following are deactivating but orth, para

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  6. Choose the correct statements :

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  7. Identify the compounds that will undergo nucleophilic aromatic substit...

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  8. Find out correct statement regarding nucleophilic aromatic substitutio...

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  9. The reaction produces:

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  10. Which of the following reactions

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  11. The following conversion reaction can be carried out by using re...

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  12. Iodobenzene can be obtained by :

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  13. Complete the following reaction

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  14. Which of the following are deacitvating group ?

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  15. Which of the following are more reactive than diphenyl in electrophi...

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  16. Diople moment of which compound is not zero ?

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  17. Which of the following can be perpared by Remimer- Tiemann reaction di...

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  18. Isopropyl benzene can be obtained by :

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  19. Which of the following are pairs of antiaromatic species ?

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  20. Which of the following compounds are aromatic ?

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