JAMB 2019 Chemistry · Question 54
The hybridization in the compound is
Options
- A.sp and sp
- B.sp
- C.sp
- D.sp and sp
Answer: A. sp and sp
Explanation written with AI and checked against the answer key
To solve this problem, we need to look at the bonding around each carbon atom in the molecule.
Note: There appears to be a slight typo in your question. The structure is chemically impossible because carbon must form four bonds. The correct structure for this series is (butyne).
1. Analyze the concept: Hybridization
Hybridization is determined by the number of sigma () bonds and lone pairs around a central atom:
- hybridization: Occurs when a carbon atom is bonded to 4 other atoms (single bonds only).
- hybridization: Occurs when a carbon atom is bonded to 3 other atoms (one double bond).
- hybridization: Occurs when a carbon atom is bonded to 2 other atoms (one triple bond or two double bonds).
2. Step-by-step breakdown
Let's analyze the structure :
- Carbon 1 (): This carbon is bonded to 3 hydrogens and 1 carbon (all single bonds). Since it has 4 sigma bonds, it is hybridized.
- Carbon 2 (): This carbon is bonded to 2 hydrogens and 2 carbons (all single bonds). Since it has 4 sigma bonds, it is hybridized.
- Carbon 3 (): This carbon is bonded to one carbon on the left and one carbon on the right via a triple bond. It is bonded to only 2 atoms. Therefore, it is hybridized.
- Carbon 4 (): This carbon is bonded to one carbon and one hydrogen. It is bonded to only 2 atoms. Therefore, it is hybridized.
3. Conclusion
The molecule contains carbon atoms that are either hybridized or hybridized. Looking at the options provided, the combination present in the chain is and .
Option A is the best fit among the choices provided.
Exam Tip: Always count the number of atoms attached to the carbon. If it's 4 atoms, it's ; if it's 3, it's ; if it's 2, it's . Ignore the pi bonds (the second and third lines in double/triple bonds) when counting for hybridization!
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