Advertisements
Advertisements
प्रश्न
In order to prepare a 1° amine from an alkyl halide with simultaneous addition of one \[\ce{CH2}\] group in the carbon chain, the reagent used as source of nitrogen is ______.
पर्याय
Sodium amide, \[\ce{NaNH2}\]
Sodium azide, \[\ce{NaN3}\]
Potassium cyanide, \[\ce{KCN}\]
Potassium phthalimide, \[\ce{C6H4 (CO)2N– K+}\]
Advertisements
उत्तर
In order to prepare a 1° amine from an alkyl halide with simultaneous addition of one \[\ce{CH2}\] group in the carbon chain, the reagent used as source of nitrogen is Potassium cyanide, \[\ce{KCN}\].
Explanation:
Potassium cyanide, as cyanide on reduction with sodium metal in alcohol, produces amine with increased carbon atoms.
\[\ce{R - X ->[KCN - KX] R - CN ->[Na/C2H2OH] R - CH2NH2}\]
APPEARS IN
संबंधित प्रश्न
Identify the compounds 'A' and 'B' in the following equation:

Write the chemical equation involved in the following reaction:
Hoffmann-bromamide degradation reaction
How do you convert the following: C6H5CONH2 to C6H5NH2
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:
\[\ce{C6H5N2Cl ->[CuCN] A ->[H2O/H+] B ->[NH3][\Delta] C}\]
Choose the most correct option.
Which of the following compounds will dissolve in aqueous NaOH after undergoing reaction with Hinsberg reagent?
Write reactions to prepare ethanamine from Acetonitrile.
The following amines is the product of Gabriel phthalimide synthesis.
Why cannot aniline be prepared by Gabriel phthalimide synthesis?
Identify the product obtained, when benzamide is treated with bromine and aqueous sodium hydroxide.
Identify the product obtained when benzyl chloride undergoes ammonolysis in presence of excess ammonia followed by the reaction with two moles of methyl iodide.
Which of the following amines forms a clear solution when treated with benzene sulphonyl chloride and excess of potassium hydroxide?
Which of the following does NOT give carbylamine test?
Write following conversions:
nitrobenzene `->` acetanilide
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?
Identify the product ‘C’ in the following reaction.
\[\ce{Aniline ->[(CH3CH)2O][Pyridine] A ->[Br2][CH3COOH] B ->[H^+ or OH^-] C}\]
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 notes on the following:
Ammonolysis
