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Isopropylbenzene can be prepared by :...

Isopropylbenzene can be prepared by :

A

Benzene `+CH_(3)CH=CH_(2)overset(H_(2)SO_(4))rarr`

B

Benzene `+CH_(3)-underset(Cl)underset(|)(CH)-CH_(3)overset(H_(2)SO_(4))rarr`

C

Benzene `+CH_(3)underset(Cl)underset(|)CH-CH_(3)overset(AlCl_(3))rarr`

D

Benzene `+CH_(3)CH_(2)CH_(2)Clunderset(Delta)overset(AlCl_(3))rarr`

Text Solution

AI Generated Solution

The correct Answer is:
To prepare isopropylbenzene (also known as cumene), we can use several methods. Below is a step-by-step text solution based on the provided information. ### Step-by-Step Solution: 1. **Understanding the Structure of Isopropylbenzene**: - Isopropylbenzene consists of a benzene ring attached to an isopropyl group (C3H7). The isopropyl group has the structure (CH(CH3)2), meaning it has a central carbon bonded to two methyl groups and one hydrogen. 2. **Method A - Protonation of Alkene**: - In this method, benzene reacts with an alkene in the presence of sulfuric acid (H2SO4). - The alkene gets protonated to form a carbocation. For isopropylbenzene, the carbocation formed would be the isopropyl carbocation (C3H7+). - This carbocation then attacks the benzene ring, leading to the formation of isopropylbenzene. 3. **Method B - Friedel-Crafts Alkylation**: - In this method, isopropyl chloride (C3H7Cl) reacts with benzene in the presence of a Lewis acid, such as aluminum chloride (AlCl3). - The Lewis acid helps to generate the isopropyl carbocation from isopropyl chloride. - The isopropyl carbocation then attacks the benzene ring, forming isopropylbenzene. 4. **Method C - Hydride Shift**: - In this method, a primary carbocation is formed first, which is less stable. - A hydride shift occurs, where a hydrogen atom moves from an adjacent carbon to stabilize the carbocation, forming a more stable secondary isopropyl carbocation. - This secondary carbocation then attacks the benzene ring to yield isopropylbenzene. 5. **Conclusion**: - Methods A, B, and C successfully yield isopropylbenzene, while other methods may not lead to the desired product. - Therefore, the correct methods to prepare isopropylbenzene are A, B, and C. ### Final Answer: Isopropylbenzene can be prepared by methods A, B, and C. ---
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ALLEN-ALKENE, ALKANE & ALKYNE -EXERCISE-2
  1. The major product formed in the reaction is :

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  2. When nitrobenzene is treated with Br(2) in presence of FeBr(3), the m...

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  3. Isopropylbenzene can be prepared by :

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  4. Which of the following statement is true about aromatic compound?

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  5. Which among the following is a meta directing group?

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  6. How many of the following groups are ortho,para directing and ring act...

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  7. Which of the following statements are correct :

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  8. The reaction of toluene with chlorine in presence of ferric chloride g...

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  9. Explain, why does benzene not undergo addition reactions easily?

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  10. Among following statements on the nitration of aromatic compoun...

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  11. Chlorination of benzene in the presence of halogen carrier is an examp...

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  12. Benzene reacts with CH(3)Cl in the presence of anhydrous AlCl(3) to ...

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  13. Select the incorrect statement among the following

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  14. Identify the correct order of reactivity in electrophilic substitution...

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  15. The structure of Wheland intermediate obtained after the attack of Br^...

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  16. Conjugation of electron withdrawing groups, e.e., -CHO, -overset(O)ove...

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  17. Which of the following sttements is//are true

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  19. Most stable frec ratical formed at the position

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  20. Consider the following reaction. (1R,3S)-cis-Bromo-3-methylcycloh...

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