Organic Compounds Containing Nitrogen
General Characteristics and Methods of Preparation of Amines
Hoffmann's Ammonolysis
\tt H_{3}C - CH_{2} - Br \xrightarrow[-HX]{NH_{3}} H_{3}C - CH_{2} - NH_{2} \xrightarrow[]{H_{3}C - CH_{2} - I} \left(CH_{3} - CH_{2}\right)_{2}NH \xrightarrow[]{H_{3}C - CH_{2} - I}\left(C_{2}H_{5}\right)_{3}N\xrightarrow[]{C_{2}H_{5}I} \left(C_{2}H_{5}\right)_{4}NI^{+}
Good yield of Amine (If NH3 is excess)/ Not suitable for Aryl Amine)
Reactivity: R—l > R—Br > R—Cl
Gabriel/Phthalimide Synthesis:
2° & 3° → can't be prepared : Aromatic amine can't prepared
Reduction :
Hoffmann Boroamide Degradation :
Schmidt Reaction
Lossen Reaction
Preparation of aniline:-
Amides, cyanide and Isocyanide:-
Amides preparation
Preparation methods of cyanides:
Preparation methods and properties of Isocyanides:
Preparation of Nitro compounds
Part1: View the Topic in this Video from 0:50 to 55:20
Part2: View the Topic in this Video from 0:54 to 25:04
Part3: View the Topic in this Video from 41:51 to 45:55
Disclaimer: Compete.etutor.co may from time to time provide links to third party Internet sites under their respective fair use policy and it may from time to time provide materials from such third parties on this website. These third party sites and any third party materials are provided for viewers convenience and for non-commercial educational purpose only. Compete does not operate or control in any respect any information, products or services available on these third party sites. Compete.etutor.co makes no representations whatsoever concerning the content of these sites and the fact that compete.etutor.co has provided a link to such sites is NOT an endorsement, authorization, sponsorship, or affiliation by compete.etutor.co with respect to such sites, its services, the products displayed, its owners, or its providers.