JEE Exam > JEE Videos > Chemistry for JEE Main & Advanced > Short Tricks: SN2, SN1, E1 & E2 Reactions
Short Tricks: SN2, SN1, E1 & E2 Reactions Video Lecture | Chemistry for JEE Main & Advanced
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FAQs on Short Tricks: SN2, SN1, E1 & E2 Reactions Video Lecture - Chemistry for JEE Main & Advanced
| 1. What is an SN2 reaction? |  |
Ans. An SN2 (substitution nucleophilic bimolecular) reaction is a type of reaction in organic chemistry where a nucleophile replaces a leaving group in a molecule. This reaction occurs in a single step, with the nucleophile attacking the substrate and the leaving group leaving simultaneously.
| 2. How does an SN1 reaction differ from an SN2 reaction? | |
Ans. An SN1 (substitution nucleophilic unimolecular) reaction is a type of reaction in organic chemistry where the reaction proceeds through a carbocation intermediate. Unlike the SN2 reaction, the SN1 reaction occurs in two steps, with the leaving group leaving first and then the nucleophile attacking the carbocation.
| 3. What is an E1 reaction? | |
Ans. An E1 (elimination unimolecular) reaction is a type of reaction in organic chemistry where a molecule undergoes elimination to form a double bond. This reaction occurs in two steps, with the leaving group leaving first and the base abstracting a proton to form the double bond.
| 4. How is an E2 reaction different from an E1 reaction? | |
Ans. An E2 (elimination bimolecular) reaction is a type of reaction in organic chemistry where a molecule undergoes elimination to form a double bond. Unlike the E1 reaction, the E2 reaction occurs in a single step, with the base abstracting a proton while the leaving group leaves, leading to the formation of the double bond.
| 5. What are some factors that influence the outcome of SN2, SN1, E1, and E2 reactions? | |
Ans. Several factors can influence the outcome of these reactions, including the nature of the nucleophile or base, the structure of the substrate, the solvent used, and the temperature. The strength of the nucleophile or base, the steric hindrance around the reaction site, the stability of the carbocation intermediate, and the polarity of the solvent can all affect whether an SN2, SN1, E1, or E2 reaction predominates.
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Dec 22, 2024 Last updated |
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