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Answer the following Write a reaction to convert acetic acid into methylamine.

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प्रश्न

Answer the following

Write a reaction to convert acetic acid into methylamine.

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उत्तर

\[\ce{\underset{Ethanoic acid}{CH3COOH} ->[SOCl2] \underset{Ethanoyl chloride}{CH3COCl} ->[NH3 (excess)] \underset{Ethanamide}{CH3CONH2} ->[Br2/KOH][Hofmann bromamide reaction] \underset{Methylamine}{CH3NH2}}\]

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पाठ 13: Amines - Exercises [पृष्ठ २९७]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
पाठ 13 Amines
Exercises | Q 3.04 | पृष्ठ २९७

संबंधित प्रश्‍न

How is ethyl amine prepared from methyl iodide?


Write a short note on Hoffmann bromamide degradation.


How do you convert the following: C6H5CONH2 to C6H5NH2


Give the structures of A, B and C in the following reactions :


Accomplish the following conversion:

Benzyl chloride to 2-phenylethanamine


Give the structure of A, B and C in the following reaction:

\[\ce{C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C}\]


Give the structures of A, B and C in the following reaction:

\[\ce{C6H5NO2 ->[Fe/HCl] A ->[HNO2][273 K] B ->[C6H5OH] C}\]


Write the reaction of aromatic primary amine with nitrous acid.


Write the reaction of aliphatic primary amine with nitrous acid.


Explain the mechanism of action of hydroiodic acid on 3-methylbutan-2-ol.


Identify 'A' and 'B' in the following reaction and rewrite the complete reaction :


Arrange the following in the increasing order of their pKvalues:

C6H5NH2, C2H5NH2, C6H5NHCH3


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 structures of compounds A and B in each of the following reactions:


Answer the following

Explain Gabriel phthalimide synthesis.


Answer the following

Explain the ammonolysis of alkyl halides.


Write reactions to prepare ethanamine from Acetonitrile.


The following amines is the product of Gabriel phthalimide synthesis.


Write reactions to bring about the following conversions.

Acetamide to methylamine


Identify the major product (B).


What is the molar mass of the amine formed when acetamide undergoes Hofmann bromamide degradation?


\[\ce{CH3-CN ->[Na/C2H5OH]}\]

The product formed is ____________.


In aqueous phase the order of basic strength of alkylamine is ______.


Identify product B in the following reaction.

\[\ce{Aniline ->[NaNO2][HCl] A ->[KI] B}\]


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:


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?


The best reagent for converting, 2-phenylpropanamide into 1- phenylethanamine is ______.


Reduction of aromatic nitro compounds using \[\ce{Fe}\] and \[\ce{HCl}\] gives ______.


Which of the following compounds is the weakest Brönsted base?


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


How will you carry out the following conversions?


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 \[\ce{NH3}\]

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.


A primary amine is formed by an amide on treatment with bromine and alkali. The primary amine has


Which of the following compound is expected to be most basic?


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.


Which of the following compound gives pink colour on reaction with phthalic anhydride in cone. H2SO4 followed by treatment with NaOH?


Which of the following reaction DOES NOT involve Hoffmann bromamide degradation?


Which of the following amines can be prepared by Gabriel phthalimide reaction?


  1. Phenyl methenamine
  2. N, N - Dimethylaniline
  3. N - Methyl aniline
  4. Benzenamine

Choose the correct order of the basic nature of the above amines.


Amides can be converted into amines by the reaction named ______.


Identify the compo ds A and B in the following reactions:

\[\ce{A ->[Nitrating mixture] B ->[(i) Sn/cone. HCI][(ii) NaOH] Aniline}\]


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 the name of reduction product formed when ethyl cyanide is treated with sodium and alcohol.


Write short note on the following.

Ammonolysis.


Write a short note on the following:

Ammonolysis.


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