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An S(N^2) reaction occurs through the fo...

An `S_(N^2)` reaction occurs through the formation of a

A

carbocation

B

carbanion

C

free radical

D

transition state.

Text Solution

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The correct Answer is:
To solve the question regarding the mechanism of an SN2 reaction, we need to understand the characteristics of this type of reaction. Here’s a step-by-step breakdown: ### Step 1: Understand the SN2 Mechanism The SN2 (Substitution Nucleophilic Bimolecular) reaction is characterized by a single-step mechanism where the nucleophile attacks the substrate at the same time as the leaving group departs. **Hint:** Recall that SN2 reactions involve a nucleophile and a substrate, and they occur in one concerted step. ### Step 2: Identify the Transition State In an SN2 reaction, there is no formation of a stable intermediate like a carbocation. Instead, there is a transition state where the nucleophile is partially bonded to the substrate while the leaving group is partially leaving. **Hint:** Remember that the transition state is a high-energy state that cannot be isolated; it represents the point of maximum energy along the reaction pathway. ### Step 3: Recognize the Role of Bonds During the SN2 reaction, one bond is formed (between the nucleophile and the carbon) while another bond is broken (between the carbon and the leaving group). This simultaneous process is crucial to the mechanism. **Hint:** Focus on the concept of bond formation and bond breaking occurring at the same time in the reaction. ### Step 4: Conclusion Since the question asks about the formation during an SN2 reaction, the correct answer is that an SN2 reaction occurs through the formation of a transition state. **Final Answer:** The correct answer is "transition state."

To solve the question regarding the mechanism of an SN2 reaction, we need to understand the characteristics of this type of reaction. Here’s a step-by-step breakdown: ### Step 1: Understand the SN2 Mechanism The SN2 (Substitution Nucleophilic Bimolecular) reaction is characterized by a single-step mechanism where the nucleophile attacks the substrate at the same time as the leaving group departs. **Hint:** Recall that SN2 reactions involve a nucleophile and a substrate, and they occur in one concerted step. ### Step 2: Identify the Transition State ...
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Knowledge Check

  • Aliphatic nucleophilic substitution is mainly of two type S_(N)1 and S_(N)2.S_(N)2 reaction proceed with strong nucleophile in polar aprotic solvent. 3^(@) halides do not give S_(N)2 reaction. Inverted products are obtained in this reaction and mechanism of reaction occurs through the formation of transition state. S_(N)1 reaction proceed through the formation of carbocation in polar aprotic solvent. Solvent itself acts as nucleophile in this reaction. Racemization takes place in S_(N)1 reaction. Which one of the following will give S_(N)2 reaction ?

    A
    `H_3 C - underset(CH_3)underset(|)overset(CH_3)overset(|)C-Cl`
    B
    C
    D
    `H_2C = CH - Cl`
  • Aliphatic nucleophilic substitution is mainly of two type S_(N)1 and S_(N)2.S_(N)2 reaction proceed with strong nucleophile in polar aprotic solvent. 3^(@) halides do not give S_(N)2 reaction. Inverted products are obtained in this reaction and mechanism of reaction occurs through the formation of transition state. S_(N)1 reaction proceed through the formation of carbocation in polar aprotic solvent. Solvent itself acts as nucleophile in this reaction. Racemization takes place in S_(N)1 reaction. Which of the following compounds will give S_(N)1 reaction?

    A
    `Ph-underset(Cl)underset(|)overset(CH_3)overset(|) - CH_2CH_3`
    B
    `H_3C -Cl`
    C
    `H_3C - CH_2 - Br`
    D
  • Aliphatic nucleophilic substitution is mainly of two type S_(N)1 and S_(N)2.S_(N)2 reaction proceed with strong nucleophile in polar aprotic solvent. 3^(@) halides do not give S_(N)2 reaction. Inverted products are obtained in this reaction and mechanism of reaction occurs through the formation of transition state. S_(N)1 reaction proceed through the formation of carbocation in polar aprotic solvent. Solvent itself acts as nucleophile in this reaction. Racemization takes place in S_(N)1 reaction. Which one of the following will give racemised product in C_2H_5OH ?

    A
    `H_3 C- underset(CH_3)underset(|) CH - Br`
    B
    `Ph-underset(CH_3)underset(|) overset(CH_3)overset(|)C-Cl`
    C
    `Ph-underset(H)underset(|) overset(CH_3)overset(|) C -Cl`
    D
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