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प्रश्न
Write reactions to prepare ethanamine from Acetonitrile.
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उत्तर
Acetonitrile on Mendius reduction yields ethanamine.
\[\ce{\underset{\text{Acetonitrile}}{CH3 - C ≡ N} + 4[H] ->[Na/C2H5OH][or LiAlH] \underset{\text{Ethanamine}}{CH3 - CH2 - NH2}}\]
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संबंधित प्रश्न
Identify the compounds 'A' and 'B' in the following equation:
Illustrate the following reaction giving suitable example in each case:Gabriel phthalimide synthesis
Write a short note on the following:
Hoffmann’s bromamide reaction
Accomplish the following conversion:
Benzamide to toluene
Give the structure of A, B and C in the following reaction:
\[\ce{C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C}\]
Give the structure of A, B and C in the following reaction:
\[\ce{CH3CH2Br ->[KCN] A ->[LiAlH4] B ->[HNO2][0^\circ C] C}\]
Give the structures of A, B and C in the following reaction:
\[\ce{CH3COOH ->[NH3][\Delta] A ->[NaOBr] B ->[NaNO2/HCl] C}\]
Give the structures of A, B and C in the following reaction:
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[HNO2][273 K] B ->[C6H5OH] C}\]
Why cannot aromatic primary amines be prepared by Gabriel phthalimide synthesis?
Write the reaction of aromatic primary amine with nitrous acid.
Mention 'two' uses of propan-2-one.
Arrange the following in the increasing order of their pKb values:
C6H5NH2, C2H5NH2, C6H5NHCH3
Account for the following:
Gabriel phthalimide synthesis is not preferred for preparing aromatic primary amines.
Write structures of compounds A and B in each of the following reactions:
Answer the following
Explain the ammonolysis of alkyl halides.
The following amines is the product of Gabriel phthalimide synthesis.
Write reactions to bring about the following conversions.
Acetamide to methylamine
Explain Hoffmann’s exhaustive alkylation with suitable reactions.
Write reactions for the preparation of ethanamine using 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.
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, ____________.
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 does NOT give carbylamine test?
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:
Which of the following methods of preparation of amines will give same number of carbon atoms in the chain of amines as in the reactant?
Reduction of nitrobenzene by which of the following reagent gives aniline?
(i) \[\ce{Sn/HCl}\]
(ii) \[\ce{Fe/HCl}\]
(iii) \[\ce{H2 - Pd}\]
(iv) \[\ce{Sn/NH4OH}\]
What is the product when \[\ce{C6H5CH2NH2}\] reacts with \[\ce{HNO2}\]?
Suggest a route by which the following conversion can be accomplished.
Identify A and B in the following reaction.
How will you bring out the following conversion?
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.
Describe Gabriel's phthalimide synthesis. (Give reaction)
The Gabriels' phthalimide synthesis is used in the synthesis of
A primary amine is formed by an amide on treatment with bromine and alkali. The primary amine has
Ethylamine can be prepared by the action of bromine and caustic potash on which compound?
Give reasons for the following:
Ammonolysis of alkyl halides is not a good method to prepare pure primary amines.
Which of the following reaction DOES NOT involve Hoffmann bromamide degradation?
Methyl amine on reaction with chloroform in the presence of NaOH gives ______.
Which of the following amines can be prepared by Gabriel phthalimide reaction?
What is the IUPAC name of \[\ce{(CH3)2 - N - CH3}\]?
Write short note on the following:
Ammonolysis
Write a short note on the following:
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 short notes on the following:
Ammonolysis
