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The most Carbocations, carbanions, free ...

The most Carbocations, carbanions, free radicals and radical cation are reactive carbon intermediates. Their hybrid orbitals respectively are

A

`sp^(2),sp^(2),sp^(3),sp`

B

`sp^(2),sp^(2),sp,sp^(3)`

C

`sp^(2),sp^(3),sp^(2),sp`

D

`sp^(3),sp^(2),sp,sp^(2)`

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The correct Answer is:
To determine the hybrid orbitals of carbocations, carbanions, free radicals, and radical cations, we can analyze each type of reactive carbon intermediate step by step. ### Step-by-Step Solution: 1. **Carbocations**: - **Definition**: Carbocations are positively charged carbon species. - **Hybridization**: In a carbocation, the carbon atom is bonded to three other atoms and has a positive charge. The geometry around the carbon is trigonal planar. - **Conclusion**: The hybridization of carbocations is **sp²**. 2. **Carbanions**: - **Definition**: Carbanions are negatively charged carbon species. - **Hybridization**: In a carbanion, the carbon atom is bonded to three other atoms and has a lone pair of electrons. The geometry around the carbon is tetrahedral. - **Conclusion**: The hybridization of carbanions is **sp³**. 3. **Free Radicals**: - **Definition**: Free radicals are neutral species with an unpaired electron. - **Hybridization**: In a free radical, the carbon atom is bonded to three other atoms and has one unpaired electron. The geometry around the carbon is trigonal planar. - **Conclusion**: The hybridization of free radicals is **sp²**. 4. **Radical Cations**: - **Definition**: Radical cations are positively charged carbon species with an unpaired electron. - **Hybridization**: In a radical cation, the carbon atom is bonded to three other atoms and has a positive charge along with an unpaired electron. The geometry around the carbon is linear. - **Conclusion**: The hybridization of radical cations is **sp**. ### Summary of Hybridizations: - Carbocations: **sp²** - Carbanions: **sp³** - Free Radicals: **sp²** - Radical Cations: **sp** ### Final Answer: The hybrid orbitals of carbocations, carbanions, free radicals, and radical cations are respectively: **sp², sp³, sp², sp**.
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RESONANCE ENGLISH-GENERAL ORGANIC CHEMISTRY-I-PART-2(NSEC)
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  3. The pair of resonanating structures among the following is

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  4. Identity the aromatic compound from the following.

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  5. Which of the following species is aromatic?

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

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

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

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

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

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

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  12. The order of decreasing stability is :

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

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

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  15. Which of the following structure is aromatic ?

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  16. Which of the following is most stable?

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  17. How many hperconjugative structures are possible in the following carb...

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  18. Which of the following is not a resonating structure for the phenoxide...

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  19. Among the following, the compound that is both paramagnetic and colour...

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

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