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Hyperconjugation observed in...

Hyperconjugation observed in

A

B

`overset(.)CPh_(3)`

C

D

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To determine which molecules exhibit hyperconjugation, we need to understand the concept of hyperconjugation and identify the presence of alpha hydrogen atoms in the given options. Here is a step-by-step solution: ### Step 1: Understand Hyperconjugation Hyperconjugation is the interaction between the electrons in a sigma bond (usually C-H or C-C) and an adjacent empty or partially filled p-orbital or pi-orbital. This interaction leads to the stabilization of the molecule. **Hint:** Remember that hyperconjugation involves sigma bonds and adjacent empty or partially filled orbitals. ### Step 2: Identify Alpha Hydrogen Atoms For hyperconjugation to occur, the molecule must have alpha hydrogen atoms. Alpha hydrogens are those hydrogen atoms that are attached to the carbon atom adjacent to a double bond, positive charge, free radical, or negative charge. **Hint:** Look for hydrogen atoms attached to carbons next to double bonds or charged species. ### Step 3: Analyze Each Option Now, we will analyze each option to see if it contains alpha hydrogen atoms. 1. **Option 1:** The molecule has no alpha hydrogens because all hydrogens are replaced by methyl groups. Thus, it cannot exhibit hyperconjugation. **Hint:** Check for the presence of hydrogen atoms on the carbon adjacent to the reactive site. 2. **Option 2:** This molecule has a free radical. The adjacent carbon has one hydrogen atom, which is an alpha hydrogen. Therefore, this molecule can exhibit hyperconjugation. **Hint:** Identify the free radical and check the adjacent carbon for hydrogen atoms. 3. **Option 3:** Similar to option 2, this molecule has a free radical with one hydrogen atom on the adjacent carbon. Hence, it can exhibit hyperconjugation. **Hint:** Look for the free radical and count the hydrogen atoms on adjacent carbons. 4. **Option 4:** This molecule has no alpha hydrogens as all valencies of the carbon are satisfied with other groups. Thus, it cannot exhibit hyperconjugation. **Hint:** Ensure that the carbon adjacent to the reactive site has available hydrogen atoms. ### Conclusion Based on the analysis: - **Option 2 and Option 3** show hyperconjugation due to the presence of alpha hydrogen atoms. - **Option 1 and Option 4** do not show hyperconjugation as they lack alpha hydrogen atoms. **Final Answer:** Hyperconjugation is observed in Option 2 and Option 3.
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Hyperconjugation is defined as No bond resonance. The concept of hyperconjugation arose from the discovery of electron releasing pattern for alkyl groups. It involves sigma electrons of C-H bond. Greater the number of C-H bond ( alpha -hydrogen atom w.r.t. double bond) more will be hyperconjugative structures, more will be stability Heat of hydrogenation of alkene are affected by hyperconjugative effects. Which of the following is incorrect hyperconjugative structure?

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RESONANCE ENGLISH-GENERAL ORGANIC CHEMISTRY-I-PRACTICE TEST-1
  1. The minimum magnitude of heat of hydrogenation per mole of molecule is...

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  2. The decreasing order of electron density on the ring is :

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  3. Hyperconjugation observed in

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  4. The number of hyperconjugable hydrogen atoms of following species are...

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  5. In the following sets of resonating structure, lable the major contrib...

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  6. In which of the following C=C bond length is minimum?

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  7. Which of the following compounds is not aromatic ?

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  8. Which compound has least e^(-) density in benzene ring

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  9. The order of heat of hydrogenation in following compounds is:

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  10. Resonance stabilized cation is:

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  11. In HCOO^(-) , the two carbon- oxygen bonds to be of equal length. What...

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  12. Compare C-N bond length in the following :

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  13. Which of the following is false for order of -l effect :

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  14. underset("x")(H-N=C=O)harrunderset("y")(H-overset(o+)N-=C-overset(Thet...

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  15. would be :

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  16. Number of delocalized e^(-) pairs in squaric acid and dianion of squar...

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  17. Which of the following benzene ring has greater electron density than ...

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  18. Which of the following has the miximum number of resonating structure ...

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  19. Among the following the aromatic compound is

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  20. overset(Theta)overset(..)CH(2)-underset(O)underset(||)C-CH(3) and CH(2...

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