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Which of the following is the most stabl...

Which of the following is the most stable?

A

`PH_(3)C^(+)`

B

`Ph_(2)overset(+)CH`

C

`Phoverset(+)CH_(2)`

D

Tropylium cation

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The correct Answer is:
To determine which of the given compounds is the most stable carbocation, we will analyze the stability of each carbocation based on their structure and the concept of aromaticity and conjugation. ### Step-by-Step Solution: 1. **Identify the Compounds**: We have four compounds to analyze for carbocation stability. Let's denote them as Compound A, Compound B, Compound C, and Compound D. 2. **Recall the Order of Carbocation Stability**: The stability of carbocations generally follows this order: - Aromatic carbocations > Conjugated carbocations > Tertiary (3°) carbocations > Secondary (2°) carbocations > Primary (1°) carbocations. 3. **Analyze Compound A**: - Structure: C, Ph, Ph, Ph (where Ph represents a phenyl group). - This compound has three phenyl groups attached to the carbocation center, allowing for significant resonance stabilization through conjugation. - Stability: This is a conjugated carbocation with 3 phenyl groups, making it relatively stable. 4. **Analyze Compound B**: - Structure: Ph, C, H (with a carbocation). - This compound has two phenyl groups attached to the carbocation. - Stability: It has less resonance stabilization compared to Compound A. 5. **Analyze Compound C**: - Structure: Ph, C, H2+ (with a carbocation). - This compound has only one phenyl group attached to the carbocation. - Stability: It has the least resonance stabilization among the first three compounds. 6. **Analyze Compound D (Propellium Ion)**: - Structure: A seven-carbon structure with a carbocation. - This compound is planar and has alternating double bonds, allowing for extensive resonance and satisfying Huckel's rule (4n + 2 π electrons). - Stability: This compound is aromatic, which makes it the most stable due to the aromaticity of the carbocation. 7. **Conclusion**: Based on the analysis, the most stable carbocation is the one that is aromatic. Therefore, Compound D (Propellium Ion) is the most stable carbocation. ### Final Answer: The most stable carbocation is **Compound D (Propellium Ion)**. ---

To determine which of the given compounds is the most stable carbocation, we will analyze the stability of each carbocation based on their structure and the concept of aromaticity and conjugation. ### Step-by-Step Solution: 1. **Identify the Compounds**: We have four compounds to analyze for carbocation stability. Let's denote them as Compound A, Compound B, Compound C, and Compound D. 2. **Recall the Order of Carbocation Stability**: The stability of carbocations generally follows this order: - Aromatic carbocations > Conjugated carbocations > Tertiary (3°) carbocations > Secondary (2°) carbocations > Primary (1°) carbocations. ...
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