amines Flashcards

1
Q

structure of RNH2

A

pyramidal

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2
Q

why is angle less trhan 109’5 for amine

A

due to presence of unshared e-

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3
Q

why is redu with iron scrap with HCL preffered

A

Fecl2 formed gets hydoolysed to release HCL during rnx and only small amount of HCL si need to initaite rnx

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4
Q

ammonolysis

A

the process of cleavage of R-X bond by ammonia

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5
Q

why ammonolysis is disadvantageous

A

due it its production of mixture of 1o,2o,3o and quarternary ammonium salt

1o amine is obtained as amahor produt by taking large excess of ammonia

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6
Q

why cant aryl amine be prepared by GPHTSYS

A

ARyl halides do not undergo nucleophilic subtiwith anion fromed by phtalimide

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7
Q

decreasing order of BP

A

1>2>3

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8
Q

what makes maines reactive

A
  1. electronegativity btwn N and H
  2. unshared e- of N

amines behacve as nucleophle du to(2)

lewis base - amine

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9
Q

aliphatic amines are stronger bases

A

+I effectog alkyl grp
leading to hig e- densityon N atom

opposite of aryl amines- eWg of aryl decrases e- density on N and hence they are less basic thqan AMMONIA

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10
Q

how is amine stabilised by ALKYL GROUP

A

BY+ I effect it disperses the posittive charge

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11
Q

what all factors influence basisity of amines in AQUEOS STATE

A
  1. steric hinderance
  2. +I inductive efff
  3. solvation eff
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12
Q

WHY IS pKb value for aniline quite high

A

-NH2 IS DIRECTLY ATTACHED TO BEN
results in unshaare e- on N to be in conjugation with ben
so it makes e- less avalable for PROTONATION

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13
Q

order of basisity of amines in gaseous state

A

3>2>1>nh3

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14
Q

order of basisity of
1. ethannamien
2. methananime
in AQUOES state

A
  1. 2>3>1> NH3
  2. 2>1>3> NH3
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15
Q

ERG attache to aniline decreases the basicity

EWGattached to aniline increases the basicity

A

-OCH3, -CH3
-NO2,-SO3H,-COOH,-X

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16
Q

benzoylation

A

amines react with benzoyll chloride c6h5cocl

17
Q

CARBYLAMINE TEST 🐡🦐

🍎

A

SHOWN BY: primary amine (aromatic aswell)
smell foul
chcl3 + 3koh (ethanolic )
isocyanide test + 3h20 + 3kcl

18
Q

nitrous acid

A

nano2 + hcl

19
Q

quantitativ eevolution of N is used in estimation

A

protein and amino acids

20
Q

prepare benzene diazonium chloriude

A

AR-NH2 +NaNO2+ HCl (273K- 278K)

21
Q

hindsberg reagent

A

C6H5SO2Cl

22
Q

why is NEthylbenzenesulphonamide soluble in alkali

A
  • H attached to Nin sulphonamideis acidic
  • due to presense of strong EW sulphonyl grp
23
Q

why is activating affect o0f NHCOCH3 less than amino grp

A

The lone pair of electrons present on nitrogen of acetanilide interacts with the oxygen atom due to resonance. Hence, the lone pair of electrons on nitrogen is less available for donation to the benzene ring

24
Q

why does aniline dont undergo FRCD CRAFTS acrnx

A

due to salt formation with ALCL3

due to this N of aniline acquires a +ve charge an dact as deacti9vatinfg grp

25
Q

diazotisation

A

conversion of 1o aromatic amines to diazonium salt

26
Q

which diazonium salt is stable at room temp and water insoluble

A

benzenediazoniumfluoroborate

27
Q

SANDEMEYES

A

BENDIACL + CU2X2/HX-> ARYLHALIDE +N2

28
Q

GATTERMAN

A

BENDIACL + Cu/HX -> ARYL HALIDE + N2+ CuX

29
Q

COUPLING REACTN

example of electrophilic subs rnx

A

BENDIAZCL react with ph in which ph molecule at its p post is coupled with diazonium salt to fom …

30
Q

yellow dye

A

pAminoazobenzene

31
Q

orange dye

A

p- Hydroxyazobenzene

32
Q

why is substantial amount ofmnitroaniline is formed

A

due to strongly acidic medium aniline protonates to fomr anilinum ion which si diactivating ans meta directing