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Which of the following has the highest p...

Which of the following has the highest potential energy for pentane?

A

anti conformation

B

eclipsed conformation

C

gauche conformation

D

all have same potential energy

Text Solution

AI Generated Solution

The correct Answer is:
To determine which conformation of pentane has the highest potential energy, we need to analyze the three types of conformations: anti, gauche, and eclipsed. ### Step-by-Step Solution: 1. **Understanding Pentane Structure**: Pentane (C5H12) is a straight-chain alkane with five carbon atoms. Its molecular structure can be represented as CH3-CH2-CH2-CH2-CH3. 2. **Conformations of Pentane**: The three main conformations of pentane are: - **Eclipsed Conformation**: In this conformation, the hydrogen atoms on adjacent carbon atoms are aligned with each other. This results in maximum steric hindrance and torsional strain. - **Gauche Conformation**: In this staggered conformation, the hydrogen atoms on adjacent carbons are positioned at a 60-degree angle to each other. This conformation has less steric hindrance than the eclipsed conformation. - **Anti Conformation**: This is also a staggered conformation where the hydrogen atoms on adjacent carbons are positioned 180 degrees apart. This arrangement minimizes steric hindrance and is the most stable conformation. 3. **Potential Energy Analysis**: - The **Eclipsed Conformation** has the highest potential energy due to the close proximity of hydrogen atoms, leading to increased repulsion and torsional strain. - The **Gauche Conformation** has lower potential energy than the eclipsed conformation but higher than the anti conformation. - The **Anti Conformation** has the lowest potential energy as it minimizes steric interactions. 4. **Conclusion**: Therefore, among the three conformations of pentane, the **Eclipsed Conformation** has the highest potential energy. ### Final Answer: The eclipsed conformation of pentane has the highest potential energy. ---
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RESONANCE ENGLISH-STEREOISOMERISM-EXERCISE (PART II : NATIONAL STANDARD EXAMINATION IN CHEMISTRY (NSEC) STAGE-1)
  1. Which of the following is a chiral molecule?

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  2. Which of the following has the highest potential energy for pentane?

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  3. Which of the following does not exist as geometric isomers ?

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  4. Which of the following is an E isomer ?

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  5. Which of the following best describes the stability of the cis and tra...

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  6. Which of the following has the greatest angle strain ?

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  7. Which would be the most stable conformation of trans-1-ethyl-3-methylc...

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  8. The positions of the object O (real or virtual) and the image 1 (real ...

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  9. Three dimensional arrangements which ca be interconverted into one ano...

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  10. Which of the following will have the least hindered rotation about car...

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  11. Cis-trans isomerism is shown by:

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  12. The number of optical isomers for a compound having two similar asymm...

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  13. Cytoplasmic male steritiy in maize is due to defective

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  14. The above pair represents

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  15. The following stereoisomers are

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  16. The compound that has the highest dipole moment is

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  17. How many optically active stereoisomers are possible for butane -2,3-d...

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  18. The number of theoretically possible stereoisomers in the following st...

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  19. The diastereomeric pair in the following four paris of compounds is

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  20. The compound used in the treatment of lead poisoning is :

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