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Questions
Write reactions to bring about the following conversions.
Acetamide to Ethylamine
Convert, acetamide into ethyl amine.
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Solution
\[\ce{CH3CONH2 ->[LiAH4][ether] CH3CH2NH2}\]
\[\ce{CH3CONH2 + 4[H] ->[LiAH4][ether] CH3CH2NH2 + H2O}\]
RELATED QUESTIONS
Write a short note on Hoffmann bromamide degradation.
Write the chemical equation involved in the following reaction:
Hoffmann-bromamide degradation reaction
How do you convert the following: C6H5CONH2 to C6H5NH2
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Give the structure of A, B and C in the following reaction:
\[\ce{C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C}\]
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Answer in one sentence.
Which amide does produce ethanamine by Hofmann bromamide degradation reaction?
Write reactions to prepare ethanamine from Acetonitrile.
The following amines is the product of Gabriel phthalimide synthesis.
Mendius reaction is used to convert _____________
Name the process of breaking C-X bond by ammonia in preparation of amines.
Write reactions to bring about the following conversions.
Acetamide to methylamine
Why cannot aniline be prepared by Gabriel phthalimide synthesis?
Acetamide on reduction using Na/C2H5OH gives ____________.
Identify the product obtained, when benzamide is treated with bromine and aqueous sodium hydroxide.
\[\ce{CH3-CN ->[Na/C2H5OH]}\]
The product formed is ____________.
Which of the following amines forms a clear solution when treated with benzene sulphonyl chloride and excess of potassium hydroxide?
Identify the product obtained when benzamide is treated with bromine and aqueous sodium hydroxide?
Identify 'A' and 'B' in the following conversions.
\[\ce{CH3 - I ->[Alc. KCN][\Delta] A ->[Na/C2H5OH] B}\]
In aqueous phase the order of basic strength of alkylamine is ______.
Which of the following reactions does NOT yield an amine?
Given below are two statements labelled as Assertion (A) and Reason (R).
Assertion (A): Alkyl halides are insoluble in water.
Reason (R): Alkyl halides have halogen attached to sp3 hybrid carbon.
Select the most appropriate answer from the options given below:
In order to prepare a 1° amine from an alkyl halide with simultaneous addition of one \[\ce{CH2}\] group in the carbon chain, the reagent used as source of nitrogen is ______.
The best reagent for converting 2–phenylpropanamide into 2-phenylpropanamine is ______.
The best reagent for converting, 2-phenylpropanamide into 1- phenylethanamine is ______.
Hoffmann Bromamide Degradation reaction is shown by ______.
Which of the following compounds is the weakest Brönsted base?
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.\[\ce{H2 SO4}\].
What is the best reagent to convert nitrile to primary amine?
Write following conversions:
acetanilide `->` p-nitroaniline
How will you carry out the following conversions?

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.
Account for the following:
Aniline cannot be prepared by the ammonolysis of chlorobenzene under normal conditions.
Ethylamine can be prepared by the action of bromine and caustic potash on which compound?
Reduction of nitro alkanes yields which compound?
In the given reaction what is the X?
\[\begin{array}{cc}
\ce{O}\phantom{.......................}\\
||\phantom{.......................}\\
\phantom{}\ce{R - C - OH <-[H3O] Χ ->[H] RCH2NH2}
\end{array}\]
Which of the following CANNOT be prepared by ammonolysis of alkyl halide?
The amine 'A' when treated with nitrous acid gives yellow oily substance. The amine A is ______.
Identify the product ‘C’ in the following reaction.
\[\ce{Aniline ->[(CH3CH)2O][Pyridine] A ->[Br2][CH3COOH] B ->[H^+ or OH^-] C}\]
Which of the following would not be a good choice for reducing nitrobenzene to aniline?
Identify A and B in the following reaction.
\[\ce{C6H5CH2Br ->[Alco.][KCN] A ->[Na/Ethanol][reduction] B}\]
Write short note on the following:
Ammonolysis
Write a short note on Ammonolysis.
Write a short note on the following:
Ammonolysis.
Write a short note on the following:
Ammonolysis
