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An enantiomerically pure acid is treated with racemic mixture of an alcohol having one chiral carbon. The ester formed will be
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Important Questions on Organic Chemistry- Some Basic Principles and Techniques
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The major product of the following reaction is :
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In the following reaction sequence, structures of and are, respectively
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The major product in the following reaction is :
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Which of the following compound upon oxidation gives isophthalic acid?
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Aldehydes or ketones when treated with the product formed is
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Consider the following reactions:
Which of these reactions are possible?
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A solution of in toluene racemises slowly in the presence of a small amount of SbCl5, due to the formation of :
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Bromination of cyclohexene under conditions given below yields:
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The major product of the following reaction is
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The attacking reagent in the nitration of benzene is
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The compound that will react most readily with gaseous bromine has the formula:
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Which of the following statements is not correct for a nucleophile?
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The major products of the following reaction are :
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The order of stability of the following carbocations:
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The correct sequence of reagents for the following conversion will be
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In which of the following compounds, the bond ionization shall give most stable carbonium ion?
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The major product of the following reaction is:
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KI in acetone, undergoes SN2 reaction with each of P, Q, R and S. The rates of the reaction vary as
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In an reaction on chiral centres, there is:
