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In which of the following all electronic...

In which of the following all electronic effects namely inductive, mesomeric and hyperconjugative effects are present?

A

B

C

D

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The correct Answer is:
To determine which of the given options contains all three electronic effects—inductive, mesomeric, and hyperconjugative effects—let's analyze each option step by step. ### Step 1: Understand the Electronic Effects 1. **Inductive Effect (−I or +I)**: This is the permanent effect due to the electronegativity difference between atoms. Electronegative atoms withdraw electrons (−I effect), while alkyl groups donate electrons (+I effect). 2. **Mesomeric Effect (Resonance)**: This effect arises from the delocalization of π electrons across adjacent atoms or groups, leading to resonance structures. 3. **Hyperconjugative Effect**: This involves the interaction of σ bonds (usually C-H) with adjacent empty or partially filled p-orbitals or π bonds, leading to stabilization. ### Step 2: Analyze Each Option - **Option A**: - No delocalization of electrons is possible. - No mesomeric effect. - No hyperconjugation (no α-hydrogens). - No inductive effect (no electronegative atoms). - **Conclusion**: Does not exhibit any of the three effects. - **Option B**: - No delocalization of electrons is possible. - No mesomeric effect. - No hyperconjugation (no α-hydrogens). - Inductive effect present due to the presence of electronegative oxygen (−I effect) and CH₃ groups (+I effect). - **Conclusion**: Lacks mesomeric and hyperconjugative effects. - **Option C**: - No delocalization of electrons is possible. - No mesomeric effect. - No hyperconjugation (no α-hydrogens). - Inductive effect present due to the presence of electronegative oxygen (−I effect). - **Conclusion**: Lacks mesomeric and hyperconjugative effects. - **Option D**: - Hyperconjugation is possible due to the presence of α-hydrogens adjacent to a double bond. - Mesomeric effect is present as electrons can delocalize across the structure. - Inductive effect is present due to the presence of CH₃ groups (which are +I) and any electronegative atoms. - **Conclusion**: Exhibits all three effects. ### Final Answer The correct answer is **Option D**, as it contains all three electronic effects: inductive, mesomeric, and hyperconjugative.
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AAKASH INSTITUTE ENGLISH-ORGANIC CHEMISTRY: SOME BASIC PRINCIPLE AND TECHNIQUES-SECTION-B OBJECTIVE TYPE QUESTION (ONE OPTION IS CORRECT)
  1. Which of the following will have weakest indicated C-H bond?

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  2. Which of the following compounds will not dissolve in aqueous NaOH?

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  3. In which of the following all electronic effects namely inductive, mes...

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  4. Most acidic species among the following is

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  5. What is the index of hydrogen deficiencyd in the molecule C(12)H(17)NO...

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  6. Which of the following reactions will not generate a carbonion?

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  7. Which will have highest melting point?

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  8. Which of the following is the strongest base in water?

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  9. Which of the following is most acidic?

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  10. Isomers which can be interconverted through rotation around a single b...

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  11. In the given anion,-ve charge is delocalized on

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  12. The compounds are

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  13. Least stable carbocation among the following is

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  14. Which of the following compound will give blood red colour while doing...

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  15. The most stable free radical is

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  16. Which of the following group will have strongest electron donating mes...

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  17. Among the following the most stable carbocation

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  18. Most acidic species among the following is

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  19. Which of the following double bond in the given molecule is most react...

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  20. Which of the following hydrocarbon is most stable ?

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