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Question
How will you carry out the following conversion?
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Solution
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RELATED QUESTIONS
Write a short note on the following:
Hoffmann’s bromamide reaction
Accomplish the following conversion:
Nitrobenzene to benzoic acid
Give a plausible explanation for the following:
Why are amines less acidic than alcohols of comparable molecular masses?
Answer the following
Explain Gabriel phthalimide synthesis.
The end product C of the following reaction is
\[\ce{C2H5NH2 ->[HNO2] A ->[PCl5] B ->[NH3][Alcohol] C}\]
Which of the following reactions is appropriate for converting benzamide to aniline?
The reduction of alkyl cyanide with sodium and ethanol to give primary amines is, ____________.
What is the product when \[\ce{C6H5CH2NH2}\] reacts with \[\ce{HNO2}\]?
How will you carry out the following conversion?
Assertion: Hoffmann’s bromamide reaction is given by primary amines.
Reason: Primary amines are more basic than secondary amines.
Assertion: Aromatic 1° amines can be prepared by Gabriel Phthalimide Synthesis.
Reason: Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.
Which of the following reactions will not give a primary amine?
The compound X is which of the following?
\[\ce{CH3CN ->[Na + C2H5OH] x}\]
Reduction of nitro alkanes yields which compound?
C6H5CONHCH3 can be converted into C6H5CH2NHCH3 by:-
Give reasons for the following:
Ammonolysis of alkyl halides is not a good method to prepare pure primary amines.
Which of the following would not be a good choice for reducing nitrobenzene to aniline?
Amides can be converted into amines by the reaction named ______.
Identify A and B in the following reaction.
\[\ce{C6H5CH2Br ->[Alco.][KCN] A ->[Na/Ethanol][reduction] B}\]
Write a short note on the following:
Ammonolysis.
