- How would you prepare the following amines, using both Hofmann and Curtius rearrangements on a carboxylic acid derivative? (a) (b) NH₂ Jamo -CH2NH2 H3C
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- Show how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. (c) m-bromoaniline (d) m-aminobenzoic acidAccount for the following :(i) Primary amines (R-NH2) have higher boiling point than tertiary amines (R3N).(ii) Aniline does not undergo Friedel – Crafts reaction.(iii) (CH3)2NH is more basic than (CH3)3N in an aqueous solution.Give the products expected when the following tertiary amines are treated with a peroxyacid and heated.N-ethylpiperidine
- By discussing the basicities of the amine structures given below, list the basicities from large to small.a) Anilineb) Pyridinec) 4-Methoxyanilined) Diphenylaminee) PiperidineGive the products expected when the following tertiary amines are treated with a peroxyacid and heated.N,N-diethylhexan-2-amineShow how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. c) m-bromoaniline
- Rank the following amines based on basicity Rationalize the electronic effects responsible for the basicity of aminesShow how to prepare the following aromatic amines by aromatic nitration, followed by reduction. You may use benzene andtoluene as your aromatic starting materials. p-bromoanilineGive reasons for the following:(i) Aniline does not undergo Friedal-Crafts reaction.(ii) (CH3)2 NH is more basic than (CH3)3 N in an aqueous solution.(iii) Primary amines have higher boiling point than tertiary amines.
- Aliphatic amines are more basic than ammonia, whereas aromatic amines are less basic than ammonia. Is that true or false?(1) Which is the most basic amine and which is a secondary amine? (2) Which can undergo hydrolysis? (3) Which gives a diazonium salt upon reaction with HNO2, HCl at 0oC?Give the products expected when the following tertiary amines are treated with a peroxyacid and heated.cyclohexyldimethylamine