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In which delocalisation of positive char...

In which delocalisation of positive charge is possible?

A

B

C

D

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The correct Answer is:
To determine in which scenario the delocalization of positive charge is possible, we will analyze each option step by step. ### Step 1: Analyze Option A - **Structure**: A nitrogen (N) atom with three hydrogen (H) atoms and a positive charge. - **Delocalization Attempt**: If we try to delocalize the positive charge by turning a bond, we would end up with a structure where nitrogen has 10 electrons. - **Conclusion**: This is not possible because nitrogen can only accommodate a maximum of 8 electrons in its valence shell. Therefore, positive charge delocalization is not possible in option A. ### Step 2: Analyze Option B - **Structure**: A nitrogen atom with two hydrogen atoms and a double bond, along with a positive charge. - **Delocalization Attempt**: Trying to delocalize the positive charge by shifting a bond results in nitrogen again having 10 electrons. - **Conclusion**: This is also not possible, as nitrogen cannot exceed its octet. Thus, positive charge delocalization is not possible in option B. ### Step 3: Analyze Option C - **Structure**: A positively charged hydroxyl group (OH2+). - **Delocalization Attempt**: Attempting to delocalize the positive charge by breaking a bond leads to a situation where the oxygen would have more than 8 electrons. - **Conclusion**: This is not feasible since oxygen cannot accommodate more than 8 electrons. Hence, positive charge delocalization is not possible in option C. ### Step 4: Analyze Option D - **Structure**: A structure with multiple double bonds and a positive charge. - **Delocalization Attempt**: If we attempt to delocalize the positive charge by breaking a bond, we can create a double bond while maintaining the octet rule for the involved atoms. - **Conclusion**: In this case, the delocalization of positive charge is possible without violating the octet rule. Therefore, option D is the correct answer. ### Final Answer The delocalization of positive charge is possible in **Option D**. ---

To determine in which scenario the delocalization of positive charge is possible, we will analyze each option step by step. ### Step 1: Analyze Option A - **Structure**: A nitrogen (N) atom with three hydrogen (H) atoms and a positive charge. - **Delocalization Attempt**: If we try to delocalize the positive charge by turning a bond, we would end up with a structure where nitrogen has 10 electrons. - **Conclusion**: This is not possible because nitrogen can only accommodate a maximum of 8 electrons in its valence shell. Therefore, positive charge delocalization is not possible in option A. ### Step 2: Analyze Option B ...
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A2Z-SOME BASIC PRINCIPALS OF ORGANIC CHEMISTRY-Section D - Chapter End Test
  1. In which delocalisation of positive charge is possible?

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  2. Arrange the following comounds in increasing order of length of their ...

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  3. The order of heat of hydrogenation in following compounds is:

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  4. S(N)1 reaction is faster in

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  5. Which compound would be least soluble in water?

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  6. Among the following compound which can be dehydrated very easily is :

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  7. Which of the follwing is not the characteristic of the mechanism of fr...

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  8. Find the strongest acid among the following compound

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  9. Among the following the dissociation constant is highest

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  10. Which one of the following compounds is most acidic

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  11. The optically active tartaric acid is named as D-(+)- tartaric acid be...

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  12. Among the following compounds (I-II) the correct order of reaction wit...

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  13. The following reaction is described as

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  14. Which of the following is the most stable cation?

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  15. The observed dipole moment of nitromethane is highly than the dipole m...

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  16. Dehydrohalogenation in presence of OH^(-) is correct represented by

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  17. Among the following the aromatic compound is

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  18. Which of the following compounds are not arranged in order of decreasi...

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  19. Most stable carbonium ion is :

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  20. Which one of the following species is most stable

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  21. Which of the following gives most stable carbocation by dehydration

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