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When cis-but-2-ene is treated with Br(2)...

When cis-but-2-ene is treated with `Br_(2)` in `"CCl"_(4)` medium the product formed will be

A

(2R, 3S) dibromobutane

B

(2R, 3R) dibromobutane

C

(2S, 3S) dibromobutane

D

Mixture of (2R, 3R) and (2S, 3S) dibromobutane

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The correct Answer is:
To solve the question regarding the reaction of cis-but-2-ene with Br₂ in CCl₄ medium, we will follow these steps: ### Step 1: Identify the Reactant The reactant given is cis-but-2-ene. The structure of cis-but-2-ene can be represented as follows: ``` CH3 | CH3-C=C-CH2 | H ``` ### Step 2: Understand the Reaction Conditions The reaction is carried out in the presence of Br₂ and CCl₄. CCl₄ is a non-polar solvent, which facilitates the reaction by allowing the bromine molecule to remain intact and not dissociate prematurely. ### Step 3: Mechanism of Bromination When cis-but-2-ene reacts with Br₂, the following mechanism occurs: 1. **Formation of Bromonium Ion**: The double bond of cis-but-2-ene attacks one of the bromine atoms, leading to the formation of a bromonium ion. This step involves the formation of a cyclic structure where one bromine atom is temporarily bonded to both carbon atoms of the double bond. 2. **Nucleophilic Attack**: The other bromine atom (Br⁻) acts as a nucleophile and attacks the more substituted carbon of the bromonium ion. This can occur from either the front or the back side of the bromonium ion. ### Step 4: Determine the Products Since the attack can occur from either side, we will have two stereoisomers: 1. **Front Side Attack**: This will lead to one stereoisomer where the bromine atoms are on the same side (cis configuration). 2. **Back Side Attack**: This will lead to another stereoisomer where the bromine atoms are on opposite sides (trans configuration). ### Step 5: Identify the Final Products The final products of the reaction will be: - 2R,3R-Dibromobutane (from front side attack) - 2S,3S-Dibromobutane (from back side attack) ### Step 6: Conclusion Since both products are formed, the correct answer to the question is that the product formed will be a mixture of 2R,3R-Dibromobutane and 2S,3S-Dibromobutane. Thus, the answer is: **A mixture of 2R,3R-Dibromobutane and 2S,3S-Dibromobutane.** ---
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