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प्रश्न
Name the process of breaking C-X bond by ammonia in preparation of amines.
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उत्तर
The process of breaking C-X bond by ammonia in preparation of amines is known as ammonolysis.
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संबंधित प्रश्न
Illustrate the following reaction giving suitable example in each case:Gabriel phthalimide synthesis
How do you convert the following: C6H5CONH2 to C6H5NH2
How do you convert the following: Ethanenitrile to ethanamine
Give the structures of A, B and C in the following reactions :
Accomplish the following conversion:
Nitrobenzene to benzoic acid
Accomplish the following conversion:
Benzamide to toluene
Give the structure of A, B and C in the following reaction:
\[\ce{CH3CH2Br ->[KCN] A ->[LiAlH4] B ->[HNO2][0^\circ C] C}\]
Why cannot aromatic primary amines be prepared by Gabriel phthalimide synthesis?
Write the reaction of aliphatic primary amine with nitrous acid.
Give a plausible explanation for the following:
Why are amines less acidic than alcohols of comparable molecular masses?
Choose the most correct option.
Which of the following compounds will dissolve in aqueous NaOH after undergoing reaction with Hinsberg reagent?
Answer in one sentence.
Predict the product of the following reaction.
\[\ce{Nitrobenzene ->[Sn/conc.HCl]?}\]
Answer the following
Explain Gabriel phthalimide synthesis.
Write reactions to prepare ethanamine from Acetonitrile.
Write reactions to bring about the following conversions.
Acetamide to Ethylamine
Write reactions to bring about the following conversions.
Acetamide to methylamine
Write reactions for the preparation of ethanamine using Gabriel phthalimide synthesis.
Acetamide on reduction using Na/C2H5OH gives ____________.
Identify the product obtained when benzyl chloride undergoes ammonolysis in presence of excess ammonia followed by the reaction with two moles of methyl iodide.
What is the molar mass of the amine formed when acetamide undergoes Hofmann bromamide degradation?
\[\ce{CH3-CN ->[Na/C2H5OH]}\]
The product formed is ____________.
Which of the following amines forms a clear solution when treated with benzene sulphonyl chloride and excess of potassium hydroxide?
Which of the following reagents is used in Mendius reduction reaction of alkyl cyanide?
Which of the following compounds is obtained when quaternary ammonium hydroxide is strongly heated?
Which of the following does NOT give carbylamine test?
Nitro compounds are reduced by iron scrap and hydrochloric acid to yield one of the following compounds:
Benzylamine may be alkylated as shown in the following equation:
\[\ce{C6H5CH2NH2 + R - X -> C6H5CH2NHR}\]
Which of the following alkylhalides is best suited for this reaction through SN1 mechanism?
Which of the following compounds is the weakest Brönsted base?
Among the following amines, the strongest Brönsted base is:
The reagents that can be used to convert benzenediazonium chloride to benzene are:
(i) \[\ce{SnCl2/HCl}\]
(ii) \[\ce{CH3CH2OH}\]
(iii) \[\ce{H3PO2}\]
(iv) \[\ce{LiAlH4}\]
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?
Suggest a route by which the following conversion can be accomplished.
How will you bring out the following conversion?
How will you carry out the following conversion?
How will you carry out the following conversion?
Match the reactions given in Column I with the statements given in Column II.
| Column I | Column II | ||
| (i) | Ammonolysis | (a) | Amine with lesser number of carbon atoms |
| (ii) | Gabriel phthalimide synthesis | (b) | Detection test for primary amines. |
| (iii) | Hoffmann Bromamide reaction | (c) | Reaction of phthalimide with \[\ce{KOH}\] and \[\ce{R-X}\] |
| (iv) | Carbylamine reaction | (d) | Reaction of alkylhalides with \[\ce{NH3}\] |
Account for the following:
Aniline cannot be prepared by the ammonolysis of chlorobenzene under normal conditions.
A primary amine is formed by an amide on treatment with bromine and alkali. The primary amine has
In the given reaction what is the X?
\[\begin{array}{cc}
\ce{O}\phantom{.......................}\\
||\phantom{.......................}\\
\phantom{}\ce{R - C - OH <-[H3O] Χ ->[H] RCH2NH2}
\end{array}\]
Methyl amine on reaction with chloroform in the presence of NaOH gives ______.
- Phenyl methenamine
- N, N - Dimethylaniline
- N - Methyl aniline
- Benzenamine
Choose the correct order of the basic nature of the above amines.
Which of the following statement(s) is/are incorrect in case of Hofmann bromamide degradation?
Write the name of the product formed by the action of LiAlH4/ether on acetamide.
Identify the compo ds A and B in the following reactions:
\[\ce{A ->[Nitrating mixture] B ->[(i) Sn/cone. HCI][(ii) NaOH] Aniline}\]
Write a short note on the following:
Ammonolysis
Write a short note on Ammonolysis.
Write short note on the following:
Ammonolysis
Write a short note on Ammonolysis.
