Hybridization And Geometry
Hybridization of carbon in benzene is:
Select the correct option:
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More basic organic principles Practice Questions
In p-nitrophenol, nitro group reduces phenolic acidity via resonance or inductive effect?
In p-nitrophenol, nitro group reduces phenolic acidity via resonance or inductive effect?
Correct order of carbocation stability:
Correct order of carbocation stability:
Which order correctly represents decreasing +I (electron donating) inductive effect?
Which order correctly represents decreasing +I (electron donating) inductive effect?
A compound is aromatic if it is cyclic, planar, fully conjugated and contains:
A compound is aromatic if it is cyclic, planar, fully conjugated and contains:
Keto-enol tautomerism involves migration of:
Keto-enol tautomerism involves migration of:
Correct decreasing basicity order in aqueous solution:
Correct decreasing basicity order in aqueous solution:
Hyperconjugation is best described as:
Hyperconjugation is best described as:
Resonance stabilization is highest in:
Resonance stabilization is highest in:
An electrophile is best defined as species that:
An electrophile is best defined as species that:
Steric hindrance most reduces rate of which mechanism?
Steric hindrance most reduces rate of which mechanism?
Order of decreasing −I effect: NO2 > F > CH3 > H is:
Order of decreasing −I effect: NO2 > F > CH3 > H is:
Which is the correct acidity order (strongest acid first)?
Which is the correct acidity order (strongest acid first)?
About This Question
- Subject
- chemistry
- Chapter
- basic organic principles
- Topic
- hybridization and geometry
- Difficulty
- Easy
- Year
- 2025
Solution
Correct Answer:
sp2
- Definition of sp2: A central atom bonded to three other atoms with no lone pairs (or total steric number 3).
- Benzene Structure: C6H6. Each carbon atom is bonded to two other carbon atoms and one hydrogen atom.
- Orbital Usage: Three sp2 hybrid orbitals form three σ bonds around each carbon atom.
- π System: One unhybridized p-orbital remains on each carbon, perpendicular to the ring plane. These six p-orbitals overlap to form a delocalized π-electron cloud.
- Geometry: The result is a hexagonal planar structure with bond angles of 120∘.
This easy difficulty chemistry question is from the chapter basic organic principles, covering the topic of hybridization and geometry. It appeared in the 2025 exam.
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