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प्रश्न
Write reactions to bring about the following conversions.
Acetamide to methylamine
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उत्तर
\[\begin{array}{cc}
\ce{O}\phantom{.............................................................}\\
||\phantom{.............................................................}\\
\ce{\underset{\text{Acetamide}}{CH3 - C - NH2} + Br2 + 4KOH_{(aq)} ->[\Delta]\underset{\text{Methylamine}}{CH3 - NH2} + 2KBr + K2CO3 + 2H2O}\\\end{array}\]
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संबंधित प्रश्न
How is ethyl amine prepared from methyl iodide?
Write the chemical equation involved in the following reaction:
Hoffmann-bromamide degradation reaction
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
Accomplish the following conversion:
Benzyl chloride to 2-phenylethanamine
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:
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[NaNO2 + HCl][273 K] B ->[H2O/H+][\Delta] C}\]
Give the structures of A, B and C in the following reactions :
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 in one sentence.
Which amide does produce ethanamine by Hofmann bromamide degradation reaction?
Answer the following
Write a reaction to convert acetic acid into methylamine.
Answer the following
Explain the ammonolysis of alkyl halides.
Explain Hoffmann’s exhaustive alkylation with suitable reactions.
Explain the following reaction with a suitable example.
Hofmann elimination reaction
Identify compound 'B' in following series of reactions?
\[\ce{Acetonitrile ->[Na/alcohol] A ->[NaNO2/dil.HCI] B}\]
Identify the product 'A' in the following reaction.
\[\ce{Aniline ->[(CH3CO)2O][Pyridine] A}\]
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?
The reduction of alkyl cyanide with sodium and ethanol to give primary amines is, ____________.
Identify the INCORRECT statement regarding Hofmann bromamide reaction.
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.
\[\ce{Aniline ->[NaNO2][HCl] A ->[KI] B}\]
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:
Amongst the following, the strongest base in aqueous medium is ______.
The source of nitrogen in Gabriel synthesis of amines is ______.
Amongst the given set of reactants, the most appropriate for preparing 2° amine is ______.
Hoffmann Bromamide Degradation reaction is shown by ______.
Reduction of aromatic nitro compounds using \[\ce{Fe}\] and \[\ce{HCl}\] gives ______.
Under which of the following reaction conditions, aniline gives p-nitro derivative as the major product?
(i) Acetyl chloride/pyridine followed by reaction with conc.\[\ce{H2SO4 }\] + conc. \[\ce{HNO3}\].
(ii) Acetic anyhdride/pyridine followed by conc.\[\ce{H2SO4}\] + conc.\[\ce{HNO3}\].
(iii) Dil. HCl followed by reaction with conc.\[\ce{H2SO4}\] + conc.\[\ce{HNO3}\].
(iv) Reaction with conc.\[\ce{HNO3}\] + conc.\[\ce{H2 SO4}\].
Write following conversions:
nitrobenzene `->` acetanilide
How will you bring out the following conversion?
How will you carry out the following conversions?
How will you carry out the following conversions?
Assertion: Only a small amount of \[\ce{HCl}\] is required in the reduction of nitro compounds with iron scrap and \[\ce{HCl}\] in the presence of steam.
Reason: \[\ce{FeCl2}\] formed gets hydrolysed to release \[\ce{HCl}\] during the reaction.
Assertion: Aromatic 1° amines can be prepared by Gabriel Phthalimide Synthesis.
Reason: Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.
When primary amines are treated with HCl, the product obtained is which of the following?
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 amines can be prepared by Gabriel phthalimide reaction?
Which of the following would not be a good choice for reducing nitrobenzene to aniline?
Amides can be converted into amines by the reaction named ______.
Write short note on the following:
Ammonolysis
Identify the compo ds A and B in the following reactions:
\[\ce{A ->[Nitrating mixture] B ->[(i) Sn/cone. HCI][(ii) NaOH] Aniline}\]
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 short note on the following.
Ammonolysis.
