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Cyclohexene reacts with limited amount o...

Cyclohexene reacts with limited amount of bromine in the presence of light to form product X `(C_6H_9Br)`
The statement correct about X is :

A

It is racemate

B

It is a product of an addition reaction

C

It is formed through a cationic intermediate

D

It is optically active

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The correct Answer is:
To solve the question regarding the reaction of cyclohexene with bromine in the presence of light to form product X (C₆H₉Br), we will analyze the reaction step by step. ### Step-by-Step Solution: 1. **Identify the Reactants**: - The reactant is cyclohexene (C₆H₁₄), which is an alkene. 2. **Understand the Reaction Conditions**: - The reaction occurs in the presence of limited bromine and light. The presence of light suggests that a free radical mechanism is involved. 3. **Mechanism of Reaction**: - The reaction proceeds via a free radical mechanism, which involves the homolytic cleavage of the Br-Br bond due to the energy provided by light. This generates bromine radicals. 4. **Formation of the Free Radical**: - The bromine radical can then abstract a hydrogen atom from the allylic position of cyclohexene, forming an allylic radical. 5. **Bromination of the Radical**: - The allylic radical can react with another bromine molecule, leading to the substitution of a bromine atom at the allylic position. This can occur from either the front or the back side of the radical, resulting in two different stereoisomers. 6. **Formation of Product X**: - The product formed (C₆H₉Br) is a mixture of two stereoisomers due to the two possible approaches of the bromine radical. This mixture is known as a racemic mixture. 7. **Optical Activity**: - Since the product is a racemic mixture, it is optically inactive because the two enantiomers will cancel each other's optical activity. 8. **Conclusion**: - The correct statement about product X is that it is a racemic mixture. It is not a product of an addition reaction, it is formed through a cationic intermediate, and it is not optically active. ### Final Answer: The correct statement about product X (C₆H₉Br) is that it is a racemic mixture. ---
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RESONANCE ENGLISH-ORGANIC REACTION MECHANISMS - II-APSP Part - 2
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  2. The compound X in the reaction.

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  3. Cyclohexene reacts with limited amount of bromine in the presence of l...

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  5. The compound which does not react with bromine easily at room temperat...

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  6. Major product of mononitration of the following compound is :

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  7. The product obtained from the following sequence of reactions is H(3...

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  8. The product (P) of the following reaction is:

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  9. Which isomer of xylene can give three different monochloroderivatives ...

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  10. The 'product' in the above reaction is :

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  11. (I) The rate of o-nitration of the above compounds, (I) toluene, (II...

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  12. The correct name of the product obtained is

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  13. Which of the following statements is correct ?

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  14. The major product of the following reaction is

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  15. The product 'N' of the following reaction is

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  16. The best sequence of reactions for the following conversion is

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