ORAGANIC COMPOUNDS CONTAINING NITROGEN [AMINE] Flashcards
A COMPPUND WHICH GIVES OILY NITROSAMINE WITH NITROUS ACID AT LOW TEMP
DIMETHYL AMINE
WHICH OF TH FOLLOWING HAS STRONGEST BASIC CHARACTER
1]C6H5NH2
2](CH3)2NH
3](CH3)3N
4]NH3
2](CH3)NH
BENZENE DIAZOIUM CLORIDES GIVES ON HYDROLYSIS
PHENOL
IN THE RXN C6H5CHO+C6H5NH2→→ C6H5N⇉[DOBLE BOND ]CHC6H5+H2O+C6H5N⇉CHC6H5
IS KNOW AS
SCHIFF BASE
NITROBENZENE GIVES N-PHENYL HYDROXYL AMINE WHEN IT REACTS WITH
ZN/NAOH
WHICH OF MIXTURE REACTS WUTH ALC KOH KNOWN AS CARBYLAMINE RXN
TRIHALOGENTED METHANE AND PRIMARY AMINE
WHICH OF THE FOLLOWING ARE RESPONSIBLE FOR BHOPAL GAS TRAGEDY IN 1984
CH3 -N⇉C⇉O MNC
ANILINE REACTS WITH COLD NITROUS ACID [NANO2+HCL] AND GIVES
C6H5–N2–CL
THE PRODUCT OF MUSTARD OIL RXN IS
ALKYL ISOTHIOCYANTE
A NITOGEN CONTAINING COMPOUND , ON HEATING WITH CHLOROFORM AND ALCOHOLIC KOH GIVES VAPOURS OF DISAGREEABLE ODOUR THE COMPUND CAN BE
ANILINE
ETHYL AMONE REACTS WITH NITROUS ACID TO FORM
NITROGEN
OILOF MIRBANE IS
NITROBENZENE
ANILINE IS PURIFIED BY
STREAM DISTILLATION
AMINE WHICH WILL NOT REACT WIYH ACETYL CHLORIDE IS
(CH3)3N
C6H5N2CL+CUCL+HCL →→C6H5CL NAME THE RXN
SANDMEYAR RXN
THE ISOCYANIDE TEST IS GIVEN
1]1AMINE
2]2AMINE
3]PHENOL
4]3*AMINE
1*AMINE
WITH TRANSITON METAL ION AMINE ESTABLISH CO-ORDINATION BOND AND FOEM
COMPLEX ION
BY REDUCTION CYANIDES FORM —AND ISOCYANIDE FORM—
PRIMARY AMINE AND SECONDARY AMINE
BENZONIC ACID REACTS WITH HYDRAZOIC ACID TO FORM
ANILINE
ALL ALIPHATIC AMINES ARE MORE — THAN AMMONIA
BASIC
1AND 2 AMINE REACTS WITH GRIGNARD REAGENT TO FORM
ALKANE
C6H5-COOH + ——- → C6H5NH2+N2+CO2
N3HIT
TRINITROTOLUENE IS AN —- SUBSTANCE
EXPLOSIVE
ETHYLE AMINE OR METHYL AMINE IS — BASIC THAN AMMONIA
MORE
AROMATIC AMINES ARE — IN WATER
INSOLUBLE
AMINES ARE BENZOLATE IN PRESENCE OF NAOH . THIS RXN IS CALLED
SCHOTTEN -BAUMANN
BY RXN WITH NITROUS ACID 1AMINE FORMS ALCHOL AND 2AMINE FORM —
NITROSAMINE
RXN OF 2*AMINE WITH NITROUS ACID REPRESENT –
LIBERMANN NITROSO TEST
BASIC NATURE OF AMINE IS DUE TO PRESENCE OF — ON NITROGEN ATOM
LONE ELECTRON PAIR
PRIMARY AMINE ON HEATING WITH— AND — FORM ALKYL ISOCYANIDES
CHLOROFORM AND CAUSTIC ACID
MIXTURE OF TNT AND AMMONIUM NITRATE IS KNOWN AS
AMATOL
ON REACTING ANILINE WITH HCL AND NANO2 AT 0*C TEMP BENZENE DIAZONIUM CHLORIDE IS FORMED THIS IS CALLED —RXN
DIAZOTISATION
ON HEATING ALKYL ISOCYANIDE AT 250*C —- IS FORMED
ALKYL ISOCYANTE
CARBYLAMINE RXN IS USED FOR THE IDENTIFICATION OF —- AMINE
PRIMARY AMINE
ETHYL AMINE IS SOLUBLE IN WATER WHILE ANILINE IS NOT TRUE FALSE
TRUE
AROMATIC AMINES ARE LESS BASIC THAN ALIPHATIC AMINES
TURE
ALPHATIC AMINES ARE LESS BASIC THAN AMMONIA
FALSE
ALKYL NITRITE AND NITROALKANE ARE ISOMERS
TRUE
ALKYL NITIRITE ARE ESTERS OF NITROUS ACID
TRUE
METHYL ISOCYANATE IS POISNOUS
TRUE
EXPLOSIVE SUBSTANCES ARE MADE FROM NITROBENZENE
TRUE
C6H5SO2CL
HEINSBERG REAGENT
C6H5CH=N-C6H5
SCHIFF BASE
CCL3-NO2
CHLOROPICRIN
(CH3-CH2)2H-N=O
NITROSOAMINE
DIAZO TEST
AROMATIC PRIMARY AMINE
TNB AND TNT
EXPLOSIVE
CH3-NCS
SMELL OF MUSTARD OIL
CH3CN +[H]→
PRIMARY AMINE
PRODUCT FORMED BY THE RXN OF NITROUS ACID WITH ALIPHATIC PRIMARY AMINE
ALCOHOL
PRIMARY AMINE
RNH2
C6H5CH2NH2
PHENYL METHYL AMINE
C6H5NHCH3
N-METHYL BENZENEAMINE
C6H5NHC6H5
N-PHENYL BENZENAMINE
CH3 -CH2NH -CH3
N-METHYL ETHANAMINE
CH2 =CHCN
PROP-2-EN NITRILE
CH3-C(TRIPLE BOND) N
2 ETHYL PROPANE NITRILE
WHY ANILINE TURNS BLACKISH BROWN IN OPEN AIR ??
ANILINE GETS OXIDISED BY AIR
TERTAIRY AMINE DOES NOT ACETANILISED WHY ?
ACTIVE HYDROGEN MISSING
WHICH ISOMER OF C3H9N IS LEAST BASIC AND HAVING LOWEST BP ??
TERTIARY AMINE
WHICH AMINE GIVES DIAZOTIZATION RXN ??
ALL PRIMARY AROMATIC AMINES
THE COMPOUND OBTAINED WHEN PRIMARY AROMATIC AMINE WHEN HEATED WITH CHCL3 AND ALC KOH
PHENYL ISOCYANIDE
SECONDARY AMINE CAN BE IDENTIFIED BY
BY LIEBERMANN NITROSO TEST
PRIMARY NITROALKANE REACTS WITH NITROUS ACID TO FORM WHICH COMPOUND ?/
NITROLIC ACID
WHAT IS NATURE OF AMINES ?
BASICWRITE
THE NAME AND FORMULA OF HEISBERG REAGENT
BENZENE SULPHONYL CHLORIDE C6H5SO2CL
WHAT IS NITRATING MIXTURE ?
CONC HNO3 +CONC H2SO4
NITROBENZE IS KNOWN AS
OIL OF MIRBANE
WHAT IS NAME OF RXN FOR PREPARATION OF METHYL ISOCYANIDE
CARBULAMINE RX
WHAT DO 1AND 2 AMINE FORM ON REACTION WITH PHOSGENE ?
SUBSITUED UREA
WHAT IS OBTAINED BY REACTING AMINE WITH CHOLORFORM
ALKYL ISOCYANIDE
IN WHICH FORM AMINE IS USED IN ORGANIC SYNETHSIS ?
REAGENT ALKANE
WHAT DOES ETHYLAMINE FORM ON OXIDATION IN THE PRESENCE OF KMNO4 ?
ALDEHYDE
ON ADDING BR2 WATER IN AQ SOLU OF C6H5NH2 WHICH PRECIPITATE IS OBTAINED
SYMETRICAL TRIBROMOANILINE
WHICH AMINE IS OBTAINED BY THE REDUCTION OF CYANIDE IN THE PRESENCE OF PT OR NI
1*AMINE
C6H5NO2+6[H]+SN/HCL →+X+H2O WHAT IS X
C6H5NH2
CH3-COOH+N3H+H2SO4 →CH3NH2+CO2+N2 WRITE NAME OF RXN
SCHMIDT RXN
WRITE THE FORMULA OF BENZEE DIAZONIUM CHLORIDE
C6H5-N2-CL
SHORT NOTE ON SCHOTTEN BAUMANN RXN
AROMATIC ACID CHLORIDE REACTS WITH PHENOL AND ANILINE IN PRESENCE OF AQ NAOH OR PYRIDINE THE RXN IS KNOWN AS SCHOTTEN BAUMANN
WHAT IS MENDIUS RXN
REDUCTION OF ALKYL CYANIDES BY SODIUM AND ALCHOLS YEILD PRIMARY AMINE THIS RXN IS CALLED MENDIUS RXN
ETHYL AMINE IS MORE BASIC THAN AMMONIA WHY
THE VALUE OF Ka =4.5X10^-4 FOR ETHYL AMINE AND FOR AMMONIA Ka=1.8X10^-5
LARGER IS THE Kb VALUE MORE BASIC IS THE AMINE AND VICE VERSA .
SHORT NOTE ON SCHMIDT RXN
WHEN HYDRAZOIC ACID WHICH DISSOLVES IN CHOLORFORM OR BENZENE REACT WITH MONOCARBOXYLIC ACID IN PRESENCE OF H2SO4 AT 55*C PRIMARY AMINE IS OBTANIED
SHORT NOTE MUSTARD OIL RXN
WHEN ALIPHATIC PRIMARY AMINE IS HEATED WITH CARBON DISULHIDE AND HGCL2 ALKYL ISOTHIOCYANATE IS FORMED WHICH HAS SMELL LIKE MUSTARD OIL THEREFORE THIS RXN IS CALLED MUSTARD OIL RXN
GIVE HEINSBERG RXN FOR PRIMARY SECONDARY TERTIARY
THIS METHOD IS CAPABLE TO DIFFERENTIATE PRIMARY SECONDARY TERTIARY AMINES . AMINES ARE HEATED WITH BENZENE SULPHONYL CHLORIDE [HEINSBERG REAGENT] AND VARIOUS PRODUCTS ARE OBTAINED
PRIMARY AMINE = THESE FORM SULPHONAMIDE WHICH ARE SOLUBLE IN KOH
SECONDARY AMINE =SECONDARY AMINE ALSO FORM SULHOAMIDE WHICH ARE INSOLUBLE IN KOH
TERTIARY AMINE= TERTIARY AMINE DOES NOT REACT
WHY ANILINE IS LESS BASIC THAN ETHYL AMINE ??
ANILNE IS LESS BASIC THAN ETHYL OR CYCLOHEXYL AMINE AS DUE TO RESONACE OF BENXENE NULCEUS THE LONE PAIR OF ELECTRON OF NITROGEN ATOM IS ATTRACTED TOWARDS NLEUS AND GETS DELOACLISED IN THE RING
WHY AMINES ARE SOLUBLE IN WATER ??
AMINES ARE SOLUBLE IN WATER BECAUSE THEY HAVE HIGHER ELECTRONEGATIVITY ON NITROGEN ATOMS THEY FORM MAXIUM INTERMOLECULAR HYDROGEN BOND WITH WATER MOLECULES HENCE DUE TO DISSOCIATION RXN MOLECULES OF AMINE ARE ATTRACHED WITH WATER MOLECULES THATS WHY AMINES ARE SOLUBLE IN WATER
SHORT NOTE ON CARBLYAMINE
The carbylamine reaction, also known as Hofmann’s isocyanide test is a chemical test for the detection of primary amines. In this reaction, the analyte is heated with alcoholic potassium hydroxide and chloroform. If a primary amine is present, the isocyanide (carbylamine) is formed which are foul smelling substances.
SHORT NOTE ON DIAZOTISATION
The chemical process used in converting a primary aromatic amine into the corresponding diazonium salt of the amine
SHORT NOTE ON HOFMANN BROMAMIDE RXN
When an amide is treated with bromine in an aqueous or ethanolic solution of sodium hydroxide, degradation of amide takes place leading to the formation of primary amine.
SHORT NOTE ON COULPING RXN
AMILINE REACTS WITH DIAZOIUM CHLORIDE AT ICE COLD TEMP TO GIVE BRIGHT ORANGE RED DYE
AMMONOLYICS
Ammonolysis is the process of forming amines using, as amminating agents, ammonia or primary and secondary amines.
ACETYLATION
The acetylation / acylation of amines takes place when the acetyl group substitutes the active hydrogen atom(s) attached to the nitrogen atom of the amine. This can take place by the attack of acetyl chloride on ammines.