ORAGANIC COMPOUNDS CONTAINING NITROGEN [AMINE] Flashcards

(93 cards)

1
Q

A COMPPUND WHICH GIVES OILY NITROSAMINE WITH NITROUS ACID AT LOW TEMP

A

DIMETHYL AMINE

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2
Q

WHICH OF TH FOLLOWING HAS STRONGEST BASIC CHARACTER
1]C6H5NH2
2](CH3)2NH
3](CH3)3N
4]NH3

A

2](CH3)NH

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3
Q

BENZENE DIAZOIUM CLORIDES GIVES ON HYDROLYSIS

A

PHENOL

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4
Q

IN THE RXN C6H5CHO+C6H5NH2→→ C6H5N⇉[DOBLE BOND ]CHC6H5+H2O+C6H5N⇉CHC6H5
IS KNOW AS

A

SCHIFF BASE

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5
Q

NITROBENZENE GIVES N-PHENYL HYDROXYL AMINE WHEN IT REACTS WITH

A

ZN/NAOH

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6
Q

WHICH OF MIXTURE REACTS WUTH ALC KOH KNOWN AS CARBYLAMINE RXN

A

TRIHALOGENTED METHANE AND PRIMARY AMINE

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7
Q

WHICH OF THE FOLLOWING ARE RESPONSIBLE FOR BHOPAL GAS TRAGEDY IN 1984

A

CH3 -N⇉C⇉O MNC

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8
Q

ANILINE REACTS WITH COLD NITROUS ACID [NANO2+HCL] AND GIVES

A

C6H5–N2–CL

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9
Q

THE PRODUCT OF MUSTARD OIL RXN IS

A

ALKYL ISOTHIOCYANTE

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10
Q

A NITOGEN CONTAINING COMPOUND , ON HEATING WITH CHLOROFORM AND ALCOHOLIC KOH GIVES VAPOURS OF DISAGREEABLE ODOUR THE COMPUND CAN BE

A

ANILINE

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11
Q

ETHYL AMONE REACTS WITH NITROUS ACID TO FORM

A

NITROGEN

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12
Q

OILOF MIRBANE IS

A

NITROBENZENE

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13
Q

ANILINE IS PURIFIED BY

A

STREAM DISTILLATION

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14
Q

AMINE WHICH WILL NOT REACT WIYH ACETYL CHLORIDE IS

A

(CH3)3N

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15
Q

C6H5N2CL+CUCL+HCL →→C6H5CL NAME THE RXN

A

SANDMEYAR RXN

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16
Q

THE ISOCYANIDE TEST IS GIVEN
1]1AMINE
2]2
AMINE
3]PHENOL
4]3*AMINE

A

1*AMINE

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17
Q

WITH TRANSITON METAL ION AMINE ESTABLISH CO-ORDINATION BOND AND FOEM

A

COMPLEX ION

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18
Q

BY REDUCTION CYANIDES FORM —AND ISOCYANIDE FORM—

A

PRIMARY AMINE AND SECONDARY AMINE

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19
Q

BENZONIC ACID REACTS WITH HYDRAZOIC ACID TO FORM

A

ANILINE

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20
Q

ALL ALIPHATIC AMINES ARE MORE — THAN AMMONIA

A

BASIC

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21
Q

1AND 2 AMINE REACTS WITH GRIGNARD REAGENT TO FORM

A

ALKANE

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22
Q

C6H5-COOH + ——- → C6H5NH2+N2+CO2

A

N3HIT

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23
Q

TRINITROTOLUENE IS AN —- SUBSTANCE

A

EXPLOSIVE

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24
Q

ETHYLE AMINE OR METHYL AMINE IS — BASIC THAN AMMONIA

A

MORE

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25
AROMATIC AMINES ARE --- IN WATER
INSOLUBLE
26
AMINES ARE BENZOLATE IN PRESENCE OF NAOH . THIS RXN IS CALLED
SCHOTTEN -BAUMANN
27
BY RXN WITH NITROUS ACID 1*AMINE FORMS ALCHOL AND 2*AMINE FORM ---
NITROSAMINE
28
RXN OF 2*AMINE WITH NITROUS ACID REPRESENT --
LIBERMANN NITROSO TEST
29
BASIC NATURE OF AMINE IS DUE TO PRESENCE OF --- ON NITROGEN ATOM
LONE ELECTRON PAIR
30
PRIMARY AMINE ON HEATING WITH--- AND --- FORM ALKYL ISOCYANIDES
CHLOROFORM AND CAUSTIC ACID
31
MIXTURE OF TNT AND AMMONIUM NITRATE IS KNOWN AS
AMATOL
32
ON REACTING ANILINE WITH HCL AND NANO2 AT 0*C TEMP BENZENE DIAZONIUM CHLORIDE IS FORMED THIS IS CALLED ---RXN
DIAZOTISATION
33
ON HEATING ALKYL ISOCYANIDE AT 250*C ---- IS FORMED
ALKYL ISOCYANTE
34
CARBYLAMINE RXN IS USED FOR THE IDENTIFICATION OF ---- AMINE
PRIMARY AMINE
35
ETHYL AMINE IS SOLUBLE IN WATER WHILE ANILINE IS NOT TRUE FALSE
TRUE
36
AROMATIC AMINES ARE LESS BASIC THAN ALIPHATIC AMINES
TURE
37
ALPHATIC AMINES ARE LESS BASIC THAN AMMONIA
FALSE
38
ALKYL NITRITE AND NITROALKANE ARE ISOMERS
TRUE
39
ALKYL NITIRITE ARE ESTERS OF NITROUS ACID
TRUE
40
METHYL ISOCYANATE IS POISNOUS
TRUE
41
EXPLOSIVE SUBSTANCES ARE MADE FROM NITROBENZENE
TRUE
42
C6H5SO2CL
HEINSBERG REAGENT
43
C6H5CH=N-C6H5
SCHIFF BASE
44
CCL3-NO2
CHLOROPICRIN
45
(CH3-CH2)2H-N=O
NITROSOAMINE
46
DIAZO TEST
AROMATIC PRIMARY AMINE
47
TNB AND TNT
EXPLOSIVE
48
CH3-NCS
SMELL OF MUSTARD OIL
49
CH3CN +[H]→
PRIMARY AMINE
50
PRODUCT FORMED BY THE RXN OF NITROUS ACID WITH ALIPHATIC PRIMARY AMINE
ALCOHOL
51
PRIMARY AMINE
RNH2
52
C6H5CH2NH2
PHENYL METHYL AMINE
53
C6H5NHCH3
N-METHYL BENZENEAMINE
54
C6H5NHC6H5
N-PHENYL BENZENAMINE
55
CH3 -CH2NH -CH3
N-METHYL ETHANAMINE
56
CH2 =CHCN
PROP-2-EN NITRILE
57
CH3-C(TRIPLE BOND) N
2 ETHYL PROPANE NITRILE
58
WHY ANILINE TURNS BLACKISH BROWN IN OPEN AIR ??
ANILINE GETS OXIDISED BY AIR
59
TERTAIRY AMINE DOES NOT ACETANILISED WHY ?
ACTIVE HYDROGEN MISSING
60
WHICH ISOMER OF C3H9N IS LEAST BASIC AND HAVING LOWEST BP ??
TERTIARY AMINE
61
WHICH AMINE GIVES DIAZOTIZATION RXN ??
ALL PRIMARY AROMATIC AMINES
62
THE COMPOUND OBTAINED WHEN PRIMARY AROMATIC AMINE WHEN HEATED WITH CHCL3 AND ALC KOH
PHENYL ISOCYANIDE
63
SECONDARY AMINE CAN BE IDENTIFIED BY
BY LIEBERMANN NITROSO TEST
64
PRIMARY NITROALKANE REACTS WITH NITROUS ACID TO FORM WHICH COMPOUND ?/
NITROLIC ACID
65
WHAT IS NATURE OF AMINES ?
BASICWRITE
66
THE NAME AND FORMULA OF HEISBERG REAGENT
BENZENE SULPHONYL CHLORIDE C6H5SO2CL
67
WHAT IS NITRATING MIXTURE ?
CONC HNO3 +CONC H2SO4
68
NITROBENZE IS KNOWN AS
OIL OF MIRBANE
69
70
WHAT IS NAME OF RXN FOR PREPARATION OF METHYL ISOCYANIDE
CARBULAMINE RX
71
WHAT DO 1*AND 2* AMINE FORM ON REACTION WITH PHOSGENE ?
SUBSITUED UREA
72
WHAT IS OBTAINED BY REACTING AMINE WITH CHOLORFORM
ALKYL ISOCYANIDE
73
IN WHICH FORM AMINE IS USED IN ORGANIC SYNETHSIS ?
REAGENT ALKANE
74
WHAT DOES ETHYLAMINE FORM ON OXIDATION IN THE PRESENCE OF KMNO4 ?
ALDEHYDE
75
ON ADDING BR2 WATER IN AQ SOLU OF C6H5NH2 WHICH PRECIPITATE IS OBTAINED
SYMETRICAL TRIBROMOANILINE
76
WHICH AMINE IS OBTAINED BY THE REDUCTION OF CYANIDE IN THE PRESENCE OF PT OR NI
1*AMINE
77
C6H5NO2+6[H]+SN/HCL →+X+H2O WHAT IS X
C6H5NH2
78
CH3-COOH+N3H+H2SO4 →CH3NH2+CO2+N2 WRITE NAME OF RXN
SCHMIDT RXN
79
WRITE THE FORMULA OF BENZEE DIAZONIUM CHLORIDE
C6H5-N2-CL
80
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
81
WHAT IS MENDIUS RXN
REDUCTION OF ALKYL CYANIDES BY SODIUM AND ALCHOLS YEILD PRIMARY AMINE THIS RXN IS CALLED MENDIUS RXN
82
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 .
83
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
84
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
85
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
86
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
87
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
88
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.
89
SHORT NOTE ON DIAZOTISATION
The chemical process used in converting a primary aromatic amine into the corresponding diazonium salt of the amine
90
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.
91
SHORT NOTE ON COULPING RXN
AMILINE REACTS WITH DIAZOIUM CHLORIDE AT ICE COLD TEMP TO GIVE BRIGHT ORANGE RED DYE
92
AMMONOLYICS
Ammonolysis is the process of forming amines using, as amminating agents, ammonia or primary and secondary amines.
93
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.