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Question
How will you carry out the following conversions?
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Solution
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RELATED QUESTIONS
Illustrate the following reaction giving suitable example in each case:Gabriel phthalimide synthesis
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\[\ce{C6H5CH2NH2 + R - X -> C6H5CH2NHR}\]
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nitrobenzene `->` acetanilide
Assertion: Only a small amount of \[\ce{HCl}\] is required in the reduction of nitro compounds with iron scrap and \[\ce{HCl}\] in the presence of steam.
Reason: \[\ce{FeCl2}\] formed gets hydrolysed to release \[\ce{HCl}\] during the reaction.
Assertion: Aromatic 1° amines can be prepared by Gabriel Phthalimide Synthesis.
Reason: Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.
Describe Gabriel's phthalimide synthesis. (Give reaction)
In the given reaction what is the X?
\[\begin{array}{cc}
\ce{O}\phantom{.......................}\\
||\phantom{.......................}\\
\phantom{}\ce{R - C - OH <-[H3O] Χ ->[H] RCH2NH2}
\end{array}\]
Write short note on the following:
Ammonolysis
