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Which of the following show stable or ma...

Which of the following show stable or major form of tautomerism?

A

B

C

D

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The correct Answer is:
To determine which of the given compounds exhibit stable or major forms of tautomerism, we will analyze each compound step by step. ### Step 1: Analyze Compound A - **Structure**: Compound A does not have any alpha hydrogen atoms. - **Conclusion**: Tautomerism requires the presence of alpha hydrogen atoms for the hydrogen to shift and form a new isomer. Since there are no alpha hydrogens, tautomerism is not possible for Compound A. ### Step 2: Analyze Compound B - **Structure**: Compound B has alpha hydrogen atoms. - **Tautomerism Process**: The double bond will shift, and the alpha hydrogen will move to the oxygen atom, resulting in the formation of an alcohol. - **Conclusion**: The resulting compound is stable, indicating that tautomerism occurs here and is a major form. ### Step 3: Analyze Compound C - **Structure**: Compound C also has alpha hydrogen atoms. - **Tautomerism Process**: Similar to Compound B, the double bond shifts, and the alpha hydrogen moves to the oxygen. - **Stability Check**: However, the resulting compound does not follow Hückel's rule (4n + 2) and is classified as anti-aromatic, making it unstable. - **Conclusion**: Although tautomerism occurs, it leads to an unstable product. ### Step 4: Analyze Compound D - **Structure**: Compound D has multiple double bonds and alpha hydrogen atoms. - **Tautomerism Process**: The double bonds shift, and the hydrogen atoms move to the oxygen, resulting in a structure with a negative charge and an OH group. - **Stability Check**: The resulting compound exhibits extended conjugation, which is stable. - **Conclusion**: Tautomerism occurs here and is stable. ### Final Conclusion - The compounds that show stable or major forms of tautomerism are **Compound B** and **Compound D**. ### Summary of Results - **Stable Tautomerism**: - Compound B - Compound D - **Unstable Tautomerism**: - Compound A (no tautomerism) - Compound C (unstable due to anti-aromaticity)

To determine which of the given compounds exhibit stable or major forms of tautomerism, we will analyze each compound step by step. ### Step 1: Analyze Compound A - **Structure**: Compound A does not have any alpha hydrogen atoms. - **Conclusion**: Tautomerism requires the presence of alpha hydrogen atoms for the hydrogen to shift and form a new isomer. Since there are no alpha hydrogens, tautomerism is not possible for Compound A. ### Step 2: Analyze Compound B - **Structure**: Compound B has alpha hydrogen atoms. ...
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CENGAGE CHEMISTRY ENGLISH-ISOMERISM-Multiple choice questions (Exercise)
  1. Which of the following show stable or major form of tautomerism?

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  2. Keto enol tautomerism is not observed in:

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  3. Arrange the following in decreasing order of enol content: i. Diethy...

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  4. Which of the following will not show geometrical isomerism?

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  5. Which of the following will show geometrical isomerism ?

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  6. Which of the following are not resolvable?

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  7. Which of the following are resolvable ?

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  8. Which of the following is/are optically active?

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  9. The compounds are optically inactive because

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  10. The stable conformer (s) of trans-1-4- dimethyl] cyclohexane is/are:

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  11. The stable conformer (s) of cis-cyclohexane 1-3- diol is/are:

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  12. Which form (s) of cyclohexane is/are free from angle strain?

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  13. Which of the following statements is/are wrong, about the more stabili...

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  14. Which of the following methods are used for resolution ?

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  15. According to Baeyer's strain theory, which of the following is/are mos...

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  16. The angle strain in cyclohexane is :

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  17. Which of the following statements are correct?

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  18. Which of the following statement regarding 1,2- dimethylcyclopropane (...

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  19. Which of the following statements regarding 1,3- dimethyl cyclobutane ...

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  20. Which of the following statements regarding 1,3- dimethl cyclobutane i...

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