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प्रश्न
Write the order of reactivity of alkyl halides with ammonia.
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उत्तर
The order of reactivity of alkyl halides with ammonia is, R–I > R–Br > R–Cl.
संबंधित प्रश्न
Write a short note on Hoffmann bromamide degradation.
Write the chemical equation involved in the following reaction:
Hoffmann-bromamide degradation reaction
How do you convert the following: C6H5CONH2 to C6H5NH2
How do you convert the following: Ethanenitrile to ethanamine
Give the structures of A, B and C in the following reactions :
Accomplish the following conversion:
Nitrobenzene to benzoic acid
Accomplish the following conversion:
Benzyl chloride to 2-phenylethanamine
Accomplish the following conversion:
Benzamide to toluene
Identify 'A' and 'B' in the following reaction and rewrite the complete reaction :
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
Identify A and B in the following reactions.
\[\ce{C6H5CH2Br->[alco.][KCN]A ->[Na/ethanol]B.}\]
Answer the following
Write a reaction to convert acetic acid into methylamine.
Answer the following
Explain the ammonolysis of alkyl halides.
Name the process of breaking C-X bond by ammonia in preparation of amines.
Write reactions to bring about the following conversions.
Acetamide to methylamine
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.
\[\ce{Aniline ->[(CH3CO)2O][Pyridine] A}\]
The end product C of the following reaction is
\[\ce{C2H5NH2 ->[HNO2] A ->[PCl5] B ->[NH3][Alcohol] C}\]
What product is formed when \[\ce{R - C ≡ N}\] is hydrolysed?
\[\ce{CH3-CN ->[Na/C2H5OH]}\]
The product formed is ____________.
The reduction of alkyl cyanide with sodium and ethanol to give primary amines is, ____________.
Identify 'A' and 'B' in the following conversions.
\[\ce{CH3 - I ->[Alc. KCN][\Delta] A ->[Na/C2H5OH] B}\]
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.
\[\ce{Aniline ->[NaNO2][HCl] A ->[KI] B}\]
Which of the following does NOT give carbylamine test?
Quaternary ammonium salt is formed:
The source of nitrogen in Gabriel synthesis of amines is ______.
Amongst the given set of reactants, the most appropriate for preparing 2° amine is ______.
The best reagent for converting 2–phenylpropanamide into 2-phenylpropanamine is ______.
Hoffmann Bromamide Degradation reaction is shown by ______.
Which of the following compounds is the weakest Brönsted base?
Among the following amines, the strongest Brönsted base is:
Identify A and B in the following reaction.
Write following conversions:
acetanilide `->` p-nitroaniline
How will you carry out the following conversion?
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
The compound X is which of the following?
\[\ce{CH3CN ->[Na + C2H5OH] x}\]
Reduction of nitro alkanes yields which compound?
Acetamide and ethyl amide can be distinguished by reacting with.
Which of the following compound is expected to be most basic?
- Phenyl methenamine
- N, N - Dimethylaniline
- N - Methyl aniline
- Benzenamine
Choose the correct order of the basic nature of the above amines.
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 ______.
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 Ammonolysis.
Assertion: Amimonolysis of alkyl halides involves the reaction between alkyl halides and alcoholic ammonia.
Reason: Ammonolysis of alkyl halides produces secondary amines only.
