Amines
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New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (B)
Primary aliphatic amines react with nitrous acid to form aliphatic diazonium salts, which are unstable and release nitrogen gas and alcohol quantitatively.
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (C)
Methyl amine reacts with HNO3 form methanol with release of nitrogen gas and water as side products.
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (D)
The greater the electron density towards the ring, the greater its basic strength.
The electron withdrawing group reduces basic strength, whereas the electron donating group increases basic strength.
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (B)
Hoffmann invented a method for producing primary amines by treating an amide with bromine in an aqueous or ethanolic sodium hydroxide solution. An alkyl or aryl group migrates from the amide's carbonyl carbon to the nitrogen atom during this degradation reaction.
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (B)
Hoffmann bromamide reaction- it is also called degradation reaction as in this reaction primary amide group is treated with halogen first (Br) then the halogen-substituted amide product is converted to a primary amine with the release of carbon dioxide gas.
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (D)
Lithium aluminium hydride in ether is a strong reducing agent that donates its hydride ion to any C=O containing functional groups into corresponding reduced compounds. Here, the amide group is converted to an amine functional group.
LiAlH4 in ether is the best reagent for converting 2-phenylpropanamide to 2-phenylpropanamine.
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: ( C)
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (D)
Gabriel synthesis reaction:
Gabriel's synthesis is a method for producing primary amines. When phthalimide is treated with ethanolic potassium hydroxide, it forms a potassium salt of phthalimide, which when heated with an alkyl halide and then alkaline hydrolyzed yields the corresponding primary amine. This method cannot produce aromatic primary amines because aryl halides do not undergo nucleophilic substitution with the anion formed by phthalimide.
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (C)
Potassium cyanide, as cyanide on reduction with sodium metal in alcohol, produces amine with increased carbon atoms.
New answer posted
7 months agoContributor-Level 10
This is a Multiple Choice Questions as classified in NCERT Exemplar
Ans: (B)
Lithium aluminum hydride in ether is a strong reducing agent that donates its H? hydride ion to any C=O containing a functional group. In addition to LiAlH4 to aryl nitro compounds, no reaction will be observed, the desired products of amines will not be produced, rather it will form diazobenzene products.
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