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Identify 'A' and 'B' in the Following Reaction and Rewrite the Complete Reaction : - Chemistry

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प्रश्न

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

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उत्तर

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2017-2018 (March)

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संबंधित प्रश्न

How are propan-1-amine and propan-2-amine prepared from oxime?


Illustrate the following reaction giving suitable example in each case:Gabriel phthalimide synthesis


How do you convert the following: C6H5CONH2 to C6H5NH2


Accomplish the following conversion:

Nitrobenzene to benzoic acid


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

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


Why cannot aromatic primary amines be prepared by Gabriel phthalimide synthesis?


Write the reaction of aromatic primary amine with nitrous acid.


Give a plausible explanation for the following:

Why are amines less acidic than alcohols of comparable molecular masses?


Arrange the following in the increasing order of their pKvalues:

C6H5NH2, C2H5NH2, C6H5NHCH3


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

Identify A and B in the following reactions.

\[\ce{C6H5CH2Br->[alco.][KCN]A ->[Na/ethanol]B.}\]


Write reactions to prepare ethanamine from Acetonitrile.


The following amines is the product of Gabriel phthalimide synthesis.


Name the process of breaking C-X bond by ammonia in preparation of amines.


Write reactions for the preparation of ethanamine using Gabriel phthalimide synthesis.


Why cannot aniline be prepared by Gabriel phthalimide synthesis?


Identify compound 'B' in following series of reactions?

\[\ce{Acetonitrile ->[Na/alcohol] A ->[NaNO2/dil.HCI] B}\]


Acetamide on reduction using Na/C2H5OH gives ____________.


Which of the following amines exhibits maximum degree of intermolecular hydrogen bonding?


What product is formed when \[\ce{R - C ≡ N}\] is hydrolysed?


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 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?


Amongst the following, the strongest base in aqueous medium is ______.


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 best reagent for converting, 2-phenylpropanamide into 1- phenylethanamine 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) \[\ce{LiAlH4}\]


Write following conversions:

nitrobenzene `->` acetanilide


How will you bring out the following conversion?


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: Hoffmann’s bromamide reaction is given by primary amines.

Reason: Primary amines are more basic than secondary amines.


The compound X is which of the following?

\[\ce{CH3CN ->[Na + C2H5OH] x}\]


Acetamide and ethyl amide can be distinguished by reacting with.


When primary amines are treated with HCl, the product obtained is which of the following?


Which of the following CANNOT be prepared by ammonolysis of alkyl halide?


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


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.


Write a short note on the following:

Ammonolysis


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 a short note on Ammonolysis.


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