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OP TANDON-BASIC PRINCIPLES OF ORGANIC COMPOUNDS (MECHANISM OF ORGANIC REACTIONS)-OBJECTIVE QUESTIONS (Level-A)
- The hydrolysis of 2-bromo-3-methylbutane by S(N^(1)) mechanism gives m...
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- The electrophile, E^((o+)) attacks the benzene ring to generate the in...
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- Which one of the following carbanions is the least stable?
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- CH(3)CH(2)Cl undergoes homolytic fission produces:
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- Tertiary butyl chloride preferably undergo hydrolysis by:
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- In a S(N^(2)) substitution reaction of the type R-Br+Cl^(-)overset("...
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- The correct stability order for the following speceis is :
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- Arrange the carbanions, (CH(3))(3)bar(C),bar(C)Cl(3),(CH(3))(2)bar(C)H...
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- Which of the following carbocations will be more stable?
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- Arrange the following free radicals in order of decreasing stability: ...
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- The most easily hydrolysed molecule under S(N^(1)) condition is:
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- Least active electrophile is :
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- In the following carbocation, H//CH(3) that is most likely to migrate ...
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- Arrange the following resonating structures in order of increasing sta...
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- Identify a species which is not a Bronsted acid but a Lewis acid:
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- A solution of (-l)- chloro -1 phenyletane in toluene recemises slowly ...
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- The order of stability of the following carbocations: underset("I")(...
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- The hyperconjugative stabilities of tert-butyl cation and 2-butene, re...
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- KI in acetone, undergoes S(N)2 reaction with each of P,Q ,R and S The ...
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- Which of the following molecules is least resonance stabilised?
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