The most stable carbocation among the following is :
- A
- B
- C
- D
Question types
8.4. Organic chemistry reaction mechanism question types
620 questions across 1 question group — pick any mix to generate a Chemistry paper with step-by-step answer keys.
620
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Sample Questions
8.4. Organic chemistry reaction mechanism questions
One sample from each question group in this chapter. Select any group above to see the full set with answer keys.
The major product formed in dehydrohalogenation reaction of $2 -$Bromo pentane is Pent$-2-$ene. This product formation is based on ?
- ✓Saytzeffs Rule
- BHund's Rule
- CHofmann Rule
- DHuckel's Rule
Answer: A.
View full solution →Which of the following compound is most reactive in electrophilic aromatic substitution?
- ✓
- B
- C
- D
Answer: A.
View full solution →A tertiary butyl carbocation is more stable than a secondary butyl carbocation because of which of the following$?$
- ✓Hyperconjugation
- B$- I$ effect of $- CH _{3}$ groups
- C$+ R$ effect of $- CH _{3}$ groups
- D$- R$ effect of $- CH _{3}$ groups
Answer: A.
View full solution →The compound that is most difficult to protonate is
- A$H-O-H$
- B$H_3C-O-H$
- C$H_3C-O-CH_3$
- ✓$Ph-O-H$
Answer: D.
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