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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.

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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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ICSE-ORGANIC CHEMISTRY : SOME BASIC PRINCIPLES AND TECHNIQUES -OBJECTIVE ( MULTIPLE CHOICE ) TYPE QUESTIONS
  1. The reaction, RX + OH^(-) to R-OH + X^(-), is

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  2. The reaction CH3 Br + OH^(-) → CH3 OH + Br^(-) follows

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  3. An S(N^2) reaction occurs through the formation of a

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  4. The reaction, CH4+Cl2 overset("hv") to , CH3 Cl+HCl, occurs through

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  5. Which of the following acts as a nucleophile?

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  6. Which of the following has the highest nucleophilicity ? F^(-) OH^...

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  7. The order of reactivities of the following alkyl halides for an S(N^2)...

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  8. Following reaction, (CH3)3 CBr +H2O to (CH3)3 COH +HBr is an ...

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  9. Due to the presence of an unpaired electron, free radicals are

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  10. The organic chloro compound, which shows complete stereochemical inve...

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  11. Which one is a nucleophilic substitution reaction among the following ...

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  12. The order of stability of the following carbocations CH2 = underset...

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  13. The correct statement regarding electrophile is

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  14. The most suitable method of separation of 1:1 mixture of ortho and par...

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  15. Identify A and predict the type of reaction

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  16. The IUPAC name of the compound

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  17. Which of the following is correct with respect to -|-effect of the sub...

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  18. Which of the following carbocations is expected to be most stable?

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  19. Which of the following compounds will be suitable for Kjeldahl's metho...

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  20. The number of sigma (sigma ) and pi (pi) bonds in pent-2-en-4-yne is :

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