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Select the most stable carbonium ion fro...

Select the most stable carbonium ion from amongst the following

A

B

C

D

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The correct Answer is:
To determine the most stable carbonium ion from the given options, we need to analyze the structure of each carbonium ion and the substituents attached to the positively charged carbon atom. The stability of carbonium ions (also known as carbocations) is influenced by the number and type of substituents attached to the positively charged carbon. Here’s a step-by-step solution: ### Step 1: Identify the Carbonium Ions First, we need to identify the structures of the carbonium ions provided in the options. Each carbonium ion has a positive charge on a carbon atom. ### Step 2: Understand the Stability Factors The stability of carbonium ions is primarily influenced by: - **Alkyl Substitution**: More alkyl groups attached to the positively charged carbon increase stability due to the +I (inductive) effect. - **Electron Donating Effects**: Groups that can donate electron density (like alkyl groups) stabilize the positive charge. ### Step 3: Analyze Each Option Let’s analyze the options based on the number of alkyl groups attached to the positively charged carbon: 1. **Option A**: Has one alkyl group attached. 2. **Option B**: Has three alkyl groups attached. 3. **Option C**: Has two alkyl groups attached. 4. **Option D**: Has one alkyl group attached. ### Step 4: Count the +I Effects - **Option A**: 1 +I effect from one alkyl group. - **Option B**: 3 +I effects from three alkyl groups. - **Option C**: 2 +I effects from two alkyl groups. - **Option D**: 1 +I effect from one alkyl group. ### Step 5: Determine the Most Stable Carbonium Ion From the analysis: - **Option B** has the highest number of +I effects (3), which means it has the most electron-donating groups stabilizing the positive charge. Therefore, it is the most stable carbonium ion. ### Conclusion The most stable carbonium ion among the options is **Option B**. ---
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RESONANCE ENGLISH-GENERAL ORGANIC CHEMISTRY-I-PART-2(NSEC)
  1. Which of the following is true about the cycloheptatrienyl free radica...

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  2. Select the most stable carbonium ion from amongst the following

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  3. Which of the following pairs represents resonating structures ?

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  4. The aromatic compound would be

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  5. Inductive effect is a polarisation of a

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  6. Match the resonance energies 67, 88 and 121 kJ "mol"^(-1) for the foll...

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  7. The pair of resonanating structures among the following is

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  8. Identity the aromatic compound from the following.

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  9. Which of the following species is aromatic?

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  10. The number of pi electrons required for a planar cyclic conjugated sys...

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  11. Following is an example of CH(2)=CH-overset(O)overset(||)CHharrover...

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  12. The relative stabilites of the following carbocations is : H(2)"CO C...

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  13. Identify the odd species out (which of the species among the following...

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  14. Which of the following represents the true order of bond dissociation ...

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  15. The correct order of dipole moment for the following molecules is

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  16. The order of decreasing stability is :

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  17. The most Carbocations, carbanions, free radicals and radical cation ar...

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  18. The electronegativities of acetylene, ethylene and ethane are in the o...

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  19. Which of the following structure is aromatic ?

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  20. Which of the following is most stable?

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