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Question Image  Rearranged Carbocation +AgBr

The rearranged Carbocation is

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Important Questions on Organic Chemistry- Some Basic Principles and Techniques

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When trans-3-Methyl-2,3-epoxy pentane treated with aqueous acid:

Question Image  trans-3-Methyl-2,3-epoxy pentane

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Which reaction results in the formation of a pair of enantiomers?
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Which of the following reaction is/are not feasible?
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Which of the following reactions takes place by SN2 mechanism?
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The relative rates of nucleophilic substitution for the given substrates are as follows:
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Which of the following is/are correct regarding the given reaction?

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In the given reaction, the percentage of (-) enantiomer formed is:

CH3-CHI-CH2-CH3I-CH3-CHI-CH2CH3αobs=-15.90°                   αobs=-15.26°