Synthesis of Secondary and Tertiary Amines
Trending Questions
Q.
Both lithium and magnesium display several similar properties due to the diagonal relationship; However, the incorrect one is:
Both form nitrides.
Nitrates of both and yield and on heating.
Both form basic carbonates.
Both form soluble bicarbonates.
Q. Based on the reaction given above, choose the correct options:
- The products are stereoisomers
- The products are constitutional isomers
- The reaction proceeds via electrophilic aromatic substitution
- The mechanism involves a benzyne intermediate
Q. Based on the reaction given above, choose the correct options:
- The products are stereoisomers
- The products are constitutional isomers
- The reaction proceeds via electrophilic aromatic substitution
- The mechanism involves a benzyne intermediate
Q.
When methyl iodide is heated with ammonia, the product obtained is
- Methylamine
Dimethylamine
Trimethylamine
- All of the above.
Q. A hydrocarbon A(C4H8) on reaction withHCl gives a compound B(C4H9Cl) which on reaction with 1 mole of NH3 gives a compound C(C4H11N). On reacting with NaNO2 and HCl (low temperature) followed by treatment with water, compound C yields optically active alcohol(s). Ozonolysis of A(1 mole) gives 2 moles of acetaldehyde.
The compound C is:
The compound C is:
- Butan-2-amine
- N, N-dimethylethanamine
- Diethylamine
- Butylamine
Q. Choose the correct answer form the alternatives given.
NH4Cl+(A)→Microcosmicsalt
↓Heat
(B)Heat−−−−→+MnO(C)
Violet bead
(A), (B) and (C) respectively are :
NH4Cl+(A)→Microcosmicsalt
↓Heat
(B)Heat−−−−→+MnO(C)
Violet bead
(A), (B) and (C) respectively are :
- Na3PO4, NaPO3, (Mn)3(PO4)2
- Na2HPO4, Na3PO4, Mn3(PO4)2
- Na2HPO4, NaPO3, Mn(PO3)2
- Na2HPO4, NaPO3, NaMnPO4
Q. Butanedial+Ammonium carbonate△−→P
Then:
Then:
- P is aromatic
- P is antiaromatic
- P on reaction with chloroform and sodium hydroxide gives:
- P on reaction with chloroform and sodium hydroxide gives:
Q. What happens when ethylamine is made to react with excess formic acid and formaldehyde?
- The intermediate is a secondary amine
- The final product is a tertiary amine
- This reaction is called Eschweiler-Clarke methylation
- The mechanism involves reductive amination