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Which reaction results in the formation of a pair of enantiomers?

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Important Questions on Organic Chemistry- Some Basic Principles and Techniques

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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°

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For the reaction: R-X+OH-R-OH+X-, the rate expression is given as rate =6.0×10-5[R-X][OH-]+2×10-7[R-X]. What percentage of R-X react by the SN2 mechanism when [OH-]=0.01 molar.
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In the presence of an anthraquinone derivative as a catalyst, the aqueous solution of sodium dithionite Na2S2O4 (Fieser's solution) effectively removes oxygen and forms
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Organic compounds sometimes adjust their electronic as well as steric structures to attain stability. Among the following, the compound having the highest dipole moment is :