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1. Which of the following is known as Baker-Nathan 8. The correct order for the stability of given
effect? carbocation is
(1) Mesomeric effect
(2) Inductive effect
(3) Hyperconjugation
(4) Electromeric effect
5. Larger the number of hyperconjugation structures, 11. Hyperconjugation is most useful for stabilizing
the stability of free carbocation will __________ which of the following carbocations?
(1) Increase (1) Neo-pentyl (2) tert-Butyl
(2) Decrease (3) Iso-propyl (4) Ethyl
(3) Remains same
(4) None of the mentioned 12. The hyperconjugative stabilities of tert-butyl cation
and 2-butene, respectively, are due to
6. The most stable carbocation is
(1) → (empty) and → * electron
(1) (CH3)3C (2) (CH3)2C delocalisations
(3) CH3CH2 (4) CH3 (2) → * and → electron delocalisations
(3) → (filled) and → electron delocalisations
7. The correct order for the stability of given alkenes (4) (filled) → * and → * electron
is delocalisations
14. The stability of 2, 3-dimethyl but-2-ene is more than 17. Hyperconjugation involves delocalization of
2-butene. This can be explained in terms of (1) -electron
(1) Resonance
(2) -electron
(2) Hyperconjugation
(3) Electromeric effect (3) Both and -electron
(4) Inductive effect (4) Proton
15. Who pointed out the concept of hyperconjugation? 18. Hyperconjugation is also known as
(1) Nathan & Baker (2) Mulliken (1) Baker-Nathan effect
(3) Kekule (4) Kolbe (2) No bond resonance
(3) Anchimeric effect
16. Hyperconjugation is (4) All of these
(1) - conjugation
(2)Delocalization of and bonds
(3) No bond resonance
(4) All of the above
3
Note: Kindly find the Video Solution of DPPs Questions in the DPPs Section.
Answer Key
1. (3) 10. (2)
2. (1) 11. (2)
3. (2) 12. (1)
4. (2) 13. (2)
5. (1) 14. (2)
6. (1) 15. (1)
7. (3) 16. (4)
8. (2) 17. (1)
9. (4) 18. (1)
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