Advertisements
Advertisements
प्रश्न
Write the name of reduction product formed when ethyl cyanide is treated with sodium and alcohol.
Advertisements
उत्तर
Ethyl cyanide (or Propanenitrile) \[\ce{C2H5 - CN}\] after treatment with sodium and alcohol (ethanol) produces n-propyl amine.
\[\ce{\underset{(Ethyl cyanide)}{CH3 - CH2 - CN} ->[Na/C2H5OH] \underset{(n-Propyl amine)}{CH3 - CH2 - CH2 - NH2}}\]
The above reduction is known as the Mendius reduction.
APPEARS IN
संबंधित प्रश्न
Write the chemical equation involved in the following reaction:
Hoffmann-bromamide degradation reaction
How do you convert the following: Ethanenitrile to ethanamine
Give the structures of A, B and C in the following reactions :
Give the structures of A, B and C in the following reactions :
Write a short note on the following:
Hoffmann’s bromamide reaction
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:
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[NaNO2 + HCl][273 K] B ->[H2O/H+][\Delta] C}\]
Explain the mechanism of action of hydroiodic acid on 3-methylbutan-2-ol.
Mention 'two' uses of propan-2-one.
Account for the following:
Gabriel phthalimide synthesis is not preferred for preparing aromatic primary amines.
Answer in one sentence.
Predict the product of the following reaction.
\[\ce{Nitrobenzene ->[Sn/conc.HCl]?}\]
Answer the following
Write a reaction to convert acetic acid into methylamine.
Write reactions to bring about the following conversions.
Acetamide to Ethylamine
Write reactions to bring about the following conversions.
Acetamide to methylamine
Why cannot aniline be prepared by Gabriel phthalimide synthesis?
Identify compound 'B' in following series of reactions?
\[\ce{Acetonitrile ->[Na/alcohol] A ->[NaNO2/dil.HCI] B}\]
Alkyl cyanides on reduction by sodium and ethanol give primary amines. This reaction is called as ____________.
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?
Identify 'A' and 'B' in the following conversions.
\[\ce{CH3 - I ->[Alc. KCN][\Delta] A ->[Na/C2H5OH] B}\]
Identify the INCORRECT statement regarding Hofmann bromamide reaction.
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?
The source of nitrogen in Gabriel synthesis of amines is ______.
Among the following amines, the strongest Brönsted base is:
Reduction of nitrobenzene by which of the following reagent gives aniline?
(i) \[\ce{Sn/HCl}\]
(ii) \[\ce{Fe/HCl}\]
(iii) \[\ce{H2 - Pd}\]
(iv) \[\ce{Sn/NH4OH}\]
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 product when \[\ce{C6H5CH2NH2}\] reacts with \[\ce{HNO2}\]?
Suggest a route by which the following conversion can be accomplished.
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 \[\ce{NH3}\] |
The compound X is which of the following?
\[\ce{CH3CN ->[Na + C2H5OH] x}\]
Acetamide and ethyl amide can be distinguished by reacting with.
A compound 'A' on reduction with iron scrap and hydrochloric acid gives compound 'B' with molecular formula C6H7N. Compound 'B' on reaction with CHCl3 and alcoholic KOH produces an obnoxious smell of carbylamine due to the formation of 'C'. Identify 'A', 'B' and 'C' and write the chemical reactions involved.
Give reasons for the following:
Ammonolysis of alkyl halides is not a good method to prepare pure primary amines.
Which of the following amines can be prepared by Gabriel phthalimide reaction?
The amine 'A' when treated with nitrous acid gives yellow oily substance. The amine A is ______.
Which of the following statement(s) is/are incorrect in case of Hofmann bromamide degradation?
What is the IUPAC name of \[\ce{(CH3)2 - N - CH3}\]?
Write the name of the product formed by the action of LiAlH4/ether on acetamide.
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.
Write a short note on the following:
Ammonolysis
