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The rate of elimination is fastest in...

The rate of elimination is fastest in

A

`Ph-CH_2-CH_2-F`

B

`Ph-undersetunderset(O)(||)C-CH_2-CH_2-F`

C

`Ph-O-CH_2-CH_2-F`

D

`CH_3-CH_2-CH_2-F`

Text Solution

AI Generated Solution

The correct Answer is:
To determine which compound has the fastest rate of elimination, we need to analyze the stability of the carbon ion intermediate formed during the elimination reaction. The stability of this carbon ion is influenced by the presence of electron-withdrawing or electron-donating groups. ### Step-by-Step Solution: 1. **Identify the Compounds**: The question provides four options, each containing a fluoride group. We need to analyze each compound to determine the effect of substituents on the rate of elimination. 2. **Understanding Elimination Mechanism**: In alkyl fluorides, elimination reactions typically proceed through a carbon ion intermediate. The stability of this carbon ion is crucial for the rate of elimination. 3. **Evaluate Each Compound**: - **Compound A**: pH CH2 CH2F - The beta carbon has a phenyl group (pH) which is not an electron-withdrawing group. This does not significantly enhance the rate of elimination. - **Compound B**: pH C(=O) CH2 CH2F - The beta carbon has a carbonyl group (C=O), which is a strong electron-withdrawing group. This enhances the stability of the carbon ion, thus increasing the rate of elimination. - **Compound C**: pH O CH2 CH2F - The beta carbon has an -O (phenolic) group which is an electron-donating group. This decreases the stability of the carbon ion, leading to a slower rate of elimination. - **Compound D**: CH3 CH2 CH2F - The beta carbon has a methyl group (CH3) which is also an electron-donating group. This further decreases the stability of the carbon ion, resulting in a slower rate of elimination. 4. **Conclusion**: Among the four compounds, Compound B (pH C(=O) CH2 CH2F) has the strongest electron-withdrawing group, which stabilizes the carbon ion intermediate the most. Therefore, it has the fastest rate of elimination. ### Final Answer: The rate of elimination is fastest in **Compound B (pH C(=O) CH2 CH2F)**. ---
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RESONANCE ENGLISH-ORGANIC REACTION MECHANISMS-IV-APSP PART-1
  1. The most probable product in the following reaction is :

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  2. Complete the following reaction

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  3. Which statement is false for elimination reaction .

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  4. Which of the following statement is correct regarding following reacti...

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  5. Substrate that show E1 reaction

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  6. Which of the following compound will give three alkenes after dehydroh...

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  7. PhSO2CH2-CH2-OMeunderset(EtOD) overset(EtO^(theta))to"product"+underse...

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  8. Complete the following reaction

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  9. Typical features of E2 involve :

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  10. An alkyl chloride produces a single alkene on reaction with sodium eth...

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  11. The relative ease of dehydration of alcohols follows following order :

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  12. Which of the following is the correct major product for given reaction...

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  13. Which of the following is a beta-elimination reaction ?

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  14. Correct order of E2//SN2 ratio is :

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  15. The product C of the following sequence is :

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  16. The major product of the following reaction is

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  17. What is the correct sequence of reagents for the following conversion ...

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  18. In which of the following reaction the single product formed is not th...

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  19. In the following reaction the correct order of percentage of products ...

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  20. The rate of elimination is fastest in

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