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प्रश्न
How are propan-1-amine and propan-2-amine prepared from oxime?
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उत्तर
The basic reaction to prepare amine from oxime is as follows:

If R1 = H and R2 = CH3CH2 then the product will be propane-1-amine.
If R1 and R2 both are CH3 then the product will be propane-2-amine.
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संबंधित प्रश्न
Identify the compounds 'A' and 'B' in the following equation:

How do you convert the following: C6H5CONH2 to C6H5NH2
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:
\[\ce{CH3CH2I ->[NaCN] A ->[OH-][Partial hydrolysis] B ->[NaOH + Br2] C}\]
Give the structure of A, B and C in the following reaction:
\[\ce{CH3CH2Br ->[KCN] A ->[LiAlH4] B ->[HNO2][0^\circ C] C}\]
Explain the mechanism of action of hydroiodic acid on 3-methylbutan-2-ol.
Mention 'two' uses of propan-2-one.
Arrange the following in the increasing order of their pKb values:
C6H5NH2, C2H5NH2, C6H5NHCH3
Give the structures of A, B and C in the following reactions :

The following amines is the product of Gabriel phthalimide synthesis.
Mendius reaction is used to convert _____________
Explain Hoffmann’s exhaustive alkylation with suitable reactions.
Write reactions for the preparation of ethanamine using Gabriel phthalimide synthesis.
Why cannot aniline be prepared by Gabriel phthalimide synthesis?
Acetamide on reduction using Na/C2H5OH gives ____________.
The end product C of the following reaction is
\[\ce{C2H5NH2 ->[HNO2] A ->[PCl5] B ->[NH3][Alcohol] C}\]
Identify the product obtained when benzyl chloride undergoes ammonolysis in presence of excess ammonia followed by the reaction with two moles of methyl iodide.
____________ can be prepared exclusively by Gabriel phthalimide synthesis.
What product is formed when \[\ce{R - C ≡ N}\] is hydrolysed?
Which of the following reactions is appropriate for converting benzamide to aniline?
Which of the following amines forms a clear solution when treated with benzene sulphonyl chloride and excess of potassium hydroxide?
The reduction of alkyl cyanide with sodium and ethanol to give primary amines is, ____________.
In aqueous phase the order of basic strength of alkylamine is ______.
Which of the following amines cannot be prepared by Gabriel phthalimide synthesis?
Identify product B in the following reaction.
\[\ce{Aniline ->[NaNO2][HCl] A ->[KI] B}\]
Which of the following reagents is used in Hofmann's elimination reaction of amines?
Which of the following compounds is obtained when quaternary ammonium hydroxide is strongly heated?
Nitro compounds are reduced by iron scrap and hydrochloric acid to yield one of the following compounds:
Quaternary ammonium salt is formed:
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 reagents would not be a good choice for reducing an aryl nitro compound to an amine?
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 ______.
Best method for preparing primary amines from alkyl halides without changing the number of carbon atoms in the chain is ______.
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) \[\ce{LiAlH4}\]
Which of the following amines can be prepared by Gabriel synthesis.
(i) Isobutyl amine
(ii) 2-Phenylethylamine
(iii) N-methylbenzylamine
(iv) Aniline
What is the best reagent to convert nitrile to primary amine?
Suggest a route by which the following conversion can be accomplished.

Write following conversions:
acetanilide `->` p-nitroaniline
How will you carry out the following conversion?

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.
In the given reaction what is the X?
\[\begin{array}{cc}
\ce{O}\phantom{.......................}\\
||\phantom{.......................}\\
\phantom{}\ce{R - C - OH <-[H3O] Χ ->[H] RCH2NH2}
\end{array}\]
C6H5CONHCH3 can be converted into C6H5CH2NHCH3 by:-
Which of the following CANNOT be prepared by ammonolysis of alkyl halide?
Which of the following reaction DOES NOT involve Hoffmann bromamide degradation?
Which of the following amines can be prepared by Gabriel phthalimide reaction?
- Phenyl methenamine
- N, N - Dimethylaniline
- N - Methyl aniline
- Benzenamine
Choose the correct order of the basic nature of the above amines.
The amine 'A' when treated with nitrous acid gives yellow oily substance. The amine A is ______.
Which of the following would not be a good choice for reducing nitrobenzene to aniline?
Write short note on the following:
Ammonolysis
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
Write short note on the following.
Ammonolysis.
Write a short note on Ammonolysis.
Assertion: Amimonolysis of alkyl halides involves the reaction between alkyl halides and alcoholic ammonia.
Reason: Ammonolysis of alkyl halides produces secondary amines only.
Write a short note on the following:
Ammonolysis
