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Question
Write structures of compounds A and B in each of the following reactions:
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Solution



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RELATED QUESTIONS
Why cannot aromatic primary amines be prepared by Gabriel phthalimide synthesis?
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The best reagent for converting 2–phenylpropanamide into 2-phenylpropanamine is ______.
Under which of the following reaction conditions, aniline gives p-nitro derivative as the major product?
(i) Acetyl chloride/pyridine followed by reaction with conc.\[\ce{H2SO4 }\] + conc. \[\ce{HNO3}\].
(ii) Acetic anyhdride/pyridine followed by conc.\[\ce{H2SO4}\] + conc.\[\ce{HNO3}\].
(iii) Dil. HCl followed by reaction with conc.\[\ce{H2SO4}\] + conc.\[\ce{HNO3}\].
(iv) Reaction with conc.\[\ce{HNO3}\] + conc.\[\ce{H2 SO4}\].
How will you bring out the following conversion?

The Gabriels' phthalimide synthesis is used in the synthesis of
Write short notes on the following:
Ammonolysis
