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प्रश्न
The best reagent for converting 2–phenylpropanamide into 2-phenylpropanamine is ______.
विकल्प
excess \[\ce{H2}\]
\[\ce{Br2}\] in aqueous \[\ce{NaOH}\]
iodine in the presence of red phosphorus
\[\ce{LiAlH4}\] in ether
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उत्तर
The best reagent for converting 2–phenylpropanamide into 2-phenylpropanamine is \[\ce{LiAlH4}\] in ether.
Explanation:

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संबंधित प्रश्न
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 structure of A, B and C in the following reaction:
\[\ce{C6H5NO2 ->[Fe/HCl] A ->[NaNO2 + HCl][273 K] B ->[H2O/H+][\Delta] C}\]
Answer the following
Write a reaction to convert acetic acid into methylamine.
Name the process of breaking C-X bond by ammonia in preparation of amines.
Identify the product obtained, when benzamide is treated with bromine and aqueous sodium hydroxide.
In aqueous phase the order of basic strength of alkylamine is ______.
Which of the following reagents is used in Hofmann's elimination reaction of amines?
Which of the following reactions does NOT yield an amine?
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?
Reduction of aromatic nitro compounds using \[\ce{Fe}\] and \[\ce{HCl}\] gives ______.
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 \[\ce{HNO2}\]?
Which of the following compound is expected to be most basic?
Write the name of the product formed by the action of LiAlH4/ether on acetamide.
Write short note on the following:
Ammonolysis
Write a short note on the following:
Ammonolysis
