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Iso -butylene can be converted into tert...

Iso -butylene can be converted into tert -butyl bromide by its reaction with

A

HBr

B

`Br_(2)`

C

HBr in the presence of peroxides

D

HOBr

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The correct Answer is:
To convert isobutylene into tert-butyl bromide, we need to follow these steps: ### Step-by-Step Solution: 1. **Identify the Structure of Isobutylene**: - Isobutylene (also known as 2-methylpropene) has the structure: \[ \text{CH}_2=C(\text{CH}_3)\text{CH}_3 \] - This structure indicates that isobutylene has a double bond between the first carbon (CH2) and the second carbon (C) which is attached to two methyl groups (CH3). 2. **Identify the Desired Product**: - The target product is tert-butyl bromide, which has the structure: \[ \text{(CH}_3)_3\text{CBr} \] - This indicates that the bromine atom is attached to a tertiary carbon that is bonded to three other carbon atoms. 3. **Analyze the Reaction Conditions**: - We have four options for reagents: A) HBr, B) Br2, C) HBr in the presence of peroxides, D) HOBr. - We need to determine which of these will lead to the formation of tert-butyl bromide. 4. **Evaluate Each Reagent**: - **Option A: HBr**: - When isobutylene reacts with HBr, it dissociates into H+ and Br-. - According to Markovnikov's rule, the H+ will add to the carbon with more hydrogen atoms, leading to the formation of a tertiary carbocation. - The Br- will then attack this tertiary carbocation, resulting in tert-butyl bromide. - **Conclusion**: This option is correct. - **Option B: Br2**: - The reaction with Br2 would lead to the formation of a dibromo compound, where bromine atoms would add across the double bond. - **Conclusion**: This option is incorrect. - **Option C: HBr in the presence of peroxides**: - In the presence of peroxides, the reaction follows a radical mechanism, leading to anti-Markovnikov addition. - This would result in the bromine attaching to the primary carbon instead of the tertiary carbon. - **Conclusion**: This option is incorrect. - **Option D: HOBr**: - HOBr would not lead to the formation of tert-butyl bromide due to the presence of oxygen, which complicates the reaction and does not favor the formation of the desired product. - **Conclusion**: This option is incorrect. 5. **Final Answer**: - The correct reagent for converting isobutylene into tert-butyl bromide is **A) HBr**.
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AAKASH INSTITUTE ENGLISH-HALOALKANES AND HALOARENES -EXERCISE
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  2. The best reagent for converting an alcohol into the corrosponding chlo...

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  3. Iso -butylene can be converted into tert -butyl bromide by its reactio...

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  4. The number of isomers possible for the molecular formula C(2) FCIBrl i...

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  5. Which of the following will react most readily with HI ?

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  7. Which of the following is most reactive towards electrophillic aromat...

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  8. Amongst the C-X bond the correct bond energy order is

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  9. Which of the following has highest boilling point ?

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  10. Out of the following compounds which one will have zero dipole moment ...

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  11. Treatment of ammonia with excess of ethyl chloride will yield

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  12. Identity Z in the following sequence

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  13. Most reactive halide towards S(N^(1)) reactions is

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  14. Which of the following is the most reactive towards nucleophilic subst...

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  16. For the reaction C(2)H(5) OH + HX to C2 H(5) X + H(2)O , the order of ...

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  17. Which of the following is not true for S(N^(1)) reaction ?

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  18. 2-Chloro-2-methylpropane on reaction with alc. KOH gives X as the prod...

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