If the carbocation rearranges to gain s...

If the carbocation rearranges to gain stability, it will rearrange to

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BRILLIANT PUBLICATION-ORGANIC CHEMISTRY : SOME BASIC PRINCIPLES - PART II (ISOMERISM AND REACTION MECHANISM) -LEVEL-II

Which will undergo fastest S(N)2 substitution reaction when treated wi...
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Under identical conditions, S(N)1 reaction will occur most efficient w...
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Consider the reaction, RCHO+NH(2)NH(2)rarrRCH=N-NH(2). What type of re...
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An incorrect statement with respect to S(N)1 and S(N)2 mechanism for a...
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In which of the following molecules, the resonance effect is not prese...
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For 1-methoxy-1, 3-butadiene, which of the following resonating struct...
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Which of the following statements regarding resonance is not correct?
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Amongst the given species, the best leaving group in a nucleophilic su...
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The mechanism of the reaction between tert-butyl alcohol and hydroxide...
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In which of the following pairs A is more stable than B?
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Which of the following carbocations will not rearrange?
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Which one of the following substitutents at para-position is most effe...
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The order of decreasing ease of abstraction of hydrogen atoms in the f...
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Which of the following reactions involves a nucleophile? (I) CH(3)CO...
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In the following carbocation, H//CH(3) that is most likely to migrate ...
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The hyperconjugative stabilities of tert-butyl cation and 2-butene, re...
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If the carbocation rearranges to gain stability, it will rearrange to
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p-chlorophenol is a stronger acid than phenol because
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The major product in the reaction is:
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Consider the following compounds: Hyperconjugation occurs in
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