All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021

CHEMISTRY : Amies & Biomolecules

46. Nitrene as an intermediate formed in the following 46. bues
al sfdl vfHkfØ; kes
aukbVªhu , d b.VjehfM,V ds:i es
a
reaction: feyrkgS%
(1) Curtius reaction (1) dfV;Zl vfHkfØ; k
(2) Schmidt reaction (2) fLeMV vfHkfØ; k
(3) Hoffmann bromamide process (3) gkW
iQ
eS
u cz
ke
skekbMfof/
(4) All (4) mi jksDr l Hkh
47. In Hoffmann Bromamide process the sequence of 47. gki Q
eS
u czks
es
ekbMi zfØ; k l s10 , ehu cukuses
acuusokys
intermediate formed in formation of 10 amine : b.VjehfM,V dkl ghØe gS%

 (1) RCON : , R–NCO, RCONHBr
(1) RCON : , R–NCO, RCONHBr
(2) RCONHBr, R–NCO, RCON
(2) RCONHBr, R–NCO, RCON
(3) RCONHBr, RCON, RNCO
(3) RCONHBr, RCON, RNCO
(4) RCON< RCONHBr, RNCO
(4) RCON< RCONHBr, RNCO
aq. KOH
aq. KOH 48. A  Hinsberg Reagent 
B   C
(Amine) (water soluble)
48. A  Hinsberg Reagent 
B   C
(Amine) (water soluble)

A o B Øe' k%gks
xsa%
A and B will be respectively :
(1) 10 , ehu vkS
j N, N-MkbZ
, Ydkby csUt hu l Yi Q
ksukekbM
(1) 10 amine and N, N-dialkyl benzene sulphonamide
(2) 10 , ehu vkS
j N-, YgkbMcsUt hu l Yi Q
ksukekbM
(2) 10 amine and N-alkyl benzene sulphonamide
(3) 20 , ehu vkS
j N, N-MkbZ
, YdkbMcsUt hu l Yi Q
ksukekbM
(3) 20 amine and N, N-dialkyl benzene sulphonamide

(4) Both 1 and 3 (4) nksuks1 vkjS3

49. 30 amine can not react with : 49. 30 , eh
u bues
al sfdl dsl kFkvfHkfØ; kughns
r k%
(1) Hinsberg reagent (1) fga
l cxZvfHkdkjd
(2) Hoffmann reagent (2) gkW
iQ
eS
u vfHkfdkjd
(3) Schiff’s reagent (3) fl i QvfHkdkjd
(4) All of these (4) mi jksDr l Hkh
50. In Hoffmann's mustard oil reaction, product will 50. gkW
iQ
eS
u eLVMZvk; y vfHkfØ; kes
amRikn gks
xk%
be :

(1) Alkyl thiocyanate

(1) , Ydkby Fkk; kslkbusV

(2) Alkyl isothiocyanide

(2) , Ydkby vkbl kF
skk; kslkbukbM
(3) Alkyl isothiocyanate (3) , Ydkby vkbl ksFkk; kslkbusV
(4) Alkyl thiocyanide (4) , Ydkby Fkk; kslkbukbM
51. Anils are formed when benzaldehyde react with : 51. , fuYl cursgSt c cs
fUt yMhgkbMfuEu l sfØ; kdjrkgS
%
(1) 10 amine (1) 10 , ehu

(2) 20 amine (2) 20 , ehu

(3) 30 amine (3) 30 , ehu
(4) all of these (4) mi jksDr l Hkh
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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021
52. On oxidation with KMnO4 20 amine give : 52. KMnO4 dsl kFkvkDl h
dj.kl s20 , ehu ns
r sgS%
(1) Tetra alkyl hydrazine (1) VsVªk, YdyhgkbMªkt hu
(2) Aldimine (2) , YMhekbu
(3) Ketimine (3) dhVhehu
(4) Dialkyl hydrazine (4) M kbZ
, Ydhy gkbMªkt hu
53. The amine formed, with one less carbon in the 53. , d de dkcZ u dh, ehu fuEu esal sfdl vfHkfØ; kl scurh
reaction: gS%
(1) Schmidt reaction (1) fLeM j vfHkfØ; k
(2) Hoffmann Bromide reaction (2) gki QeSu czksekbZ
MvfHkfØ; k
(3) Curtius reaction (3) dfVZ ;ª l vfHkfØ; k
(4) All of these (4) mi jksDr l Hkh
NH2 NH2
CF3 COOH
54.   
[O]
X, Here X will be : 54. CF3 COOH
  X, ; gkaX gS%
[O]

ONO ONO
(1) (1)

NO2 NO2
(2) (2)
F F
NO2 NO2
(3) (3)

F NH2 F NH2
(4) (4)

NH2 NH2
(i) conc. HNO3
(i) conc. HNO3
acetylation conc. H2SO4
55.  A 
B  C (ii) H2 O 55. acetylation
 conc. H2SO4
A  B  C

(ii) H2 O

B, C, A respectively will be :
B, C, A Øe' k%gS%
NHCOCH3 NH2 NH2
NHCOCH3 NH2 NH2
NO2
NO2
(1) , ,
(1) , ,
NO2
NH2 NH2 NO2
NHCOCH3 NH2 NH2
NO2 NHCOCH3
NO2
, ,
(2) , ,
(2)
NO2
NO2
NH2 NH2 NHCOCH3
NH2 NH2 NHCOCH3
NO2
NO2
, ,
(3) , ,
(3)
NO2
NO2
NHCOCH3 NH2 NH2 NHCOCH3 NH2 NH2

(4) , , , ,
(4)
NO2 NO2
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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021
[H] C2 H5 ONa [H] C2 H5 ONa
R  CN  A R  CN  A
56. [H] C2 H5 ONa 56. [H] C2 H5 ONa
R  NC  B R  NC  B

Product A and B will be respectively : mRikn A o B Øe' k%gks

xsa%
(1) R–NH–CH3 & RCH2NH2 (1) R–NH–CH3 & RCH2NH2
(2) RCH2NH2 & RNHCH3 (2) RCH2NH2 & RNHCH3
(3) RCH2NH2 & RN(CH3)2 (3) RCH2NH2 & RN(CH3)2
(4) RNH–CH3 & RCH2 NH (4) RNH–CH3 & RCH2 NH

Partial Hydrolysis
57. R–CN   A , Product A will be : Partial Hydrolysis
57. R–CN  A , mRikn A gS%
(1) RCOOH (1) RCOOH
(2) RCH2NH2 (2) RCH2NH2
(3) RCONH2 (3) RCONH2
(4) RCHO (4) RCHO

Fe/Steam Fe/Steam
NO2 A NO2 A
Zn / NH4Cl Zn / NH4Cl
58. B 58. B
Fe/HCl Fe/HCl
C C
Product C, B, A respectively will be :
mRikn C, B, A Øe' k%gks
xsa%
NO NHOH NH2
NO NHOH NH2
(1) , ,
(1) , ,
NO NH2 NHOH
NO NH2 NHOH
(2) , ,
(2) , ,
NH2 NHOH NO
NH2 NHOH NO
(3) , ,
(3) , ,
NHOH NH2 NO
NHOH NH2 NO
(4) , ,
(4) , ,
NO2
Na3AsO3 + NaOH NO2
A Na3AsO3 + NaOH
59. A
SnCl2 + NaOH 59.
B SnCl2 + NaOH
B
In product A and B the basic functional group will
be respectively : mRikn A vkS
j B es
ai k; st kusokysfØ; kRed l ew
g Øe'k%gS
%
O O
(1) –N=N–, –N=N– (2) –N=N–, –NH–NH– (1) –N=N–, –N=N– (2) –N=N–, –NH–NH–

O O O O
(3) –N=N–, –NH–NH– (4) –N=N–, –N=N– (3) –N=N–, –NH–NH– (4) –N=N–, –N=N–

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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021

NO2 NO2
(NH4 )2 S HNO2 H3PO2 (NH4 )2 S HNO2 H3PO2
60.   A 
0 50 C
 B  C 60.   A 
0 50 C
 B  C
NO2 NO2

Product A, B and C respectively will be : mRikn A, B vkS

j C Øe' k%gks
xsa%
NH2 N2Cl
NH2 N2Cl
(1)
, , (1)
NH2 NH2 NH2 , ,
NH2 NH2 NH2

NH2 N2Cl
NH2 N2Cl
NO2
NO2
(2)
, , (2)
NO2 NO2 , ,
NO2 NO2

NH2 N2Cl
NH2 N2Cl
NO2
NO2
(3)
, , (3)
NO2 NH2 , ,
NO2 NH2

NH2 NH2
NH2 NH2
(4)
, , (4)
NH2 N2Cl N2Cl , ,
NH2 N2Cl N2Cl

N2Cl
Aniline N2Cl
+ Dye-1 Aniline
H Dye-1
61. H
+
Phenol 61.
– Dye-2 Phenol
OH – Dye-2
OH

The color of Dye-1 and Dye-2 respectively : MkbZ

-1 o M
kbZ
-2 dsja
x Øe' k%gks
xsa%
(1) Yellow, Green (1) i hyk] gjk
(2) Yellow, Orange (2) i hyk] ukja
xh
(3) Orange, Yellow (3) ukja
xh] i hyk
(4) Green, Yellow (4) gjk] i hyk
62. Which of the following is correct for glucose : 62. Xyw
d ks
t dsfy, fuEu es
al sdkS
u l kl ghgS%
(1) Glucose give 2,4-DNP test (1) Xyw
d kst 2,4-DNP i jh{k.kns
r kgS
(2) does not form the hydrogen sulphite additon product (2) gkbMkªst u l Yi Q
kbM; q
Xed mRikn ughnsrkgS
(3) It give schiff's test (3) ; g f' ki Qi jh{k.knsrkgS
(4) All are correct (4) mi jkD
sr l Hkhl R; gS
63. In six memberd ring formation of glucose The 63. Xyw
d ks
t es
afl Dl es
EcMZfja
x es
] buj gS
eh,l hVy es
a–OH xzq
i
–OH group involved in inner hemiacetal is from : vkrkgS%
(1) C1 (2) C3 (1) C1 (2) C3

(3) C5 (4) C4 (3) C5 (4) C4

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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021
64. In milk sugar linkage between : 64. nq
X/ ' kdZ
j kes
acU/ i k; st krsgS%
(1) C1 of glucose and C4 of galactose (1) Xyw
d kts dsC1 vkS
j XyS
DVkst dsC4 dseè;
(2) C1 of glucose and C2 of galactose (2) Xyw
d kts dsC1 vkS
j XyS
DVkst dsC2 dseè;
(3) C1 of galactose and C2 of glucose (3) XyS
DVkst dsC1 vkS
j Xyw
d kst dsC2 dseè;
(4) C1 of galactose and C4 of glucose (4) XyS
DVkst dsC1 vkS
j Xyw
d kst dsC4 dseè;
65. In the formation of osazone how many no. of 65. vks l kt ks
u dscuuses s
] iQs
fuy gkbMªkt hu dseks
yksdhl a
[;k
moles of phenyl hydrizine required per mole of i zfr Xyw d ks
t o i zQ
s
DVks
t ] Øe' k%gksxh%
glucose and fructose respectively :
(1) 3, 2
(1) 3, 2
(2) 2, 3
(2) 2, 3
(3) 3, 3 (3) 3, 3

(4) 2, 2 (4) 2, 2
66. How many amino acids are basic in nature as given 66. uhpsfn, x, vehuksvEy es
afdrus{kkjh; gS%
below :
Isoleucine, Asparagine, Cystine, Arginine
Isoleucine, Asparagine, Cystine, Arginine
(1) 1
(1) 1
(2) 2
(2) 2
(3) 3 (3) 3

(4) 4 (4) 4
67. In acidic and basic medium amino acid moves 67. vEyh; o {kkjh; ekè; e es
avehuksvEy Øe' k%fuEu dhvks
j
towards respectively : xfr djrsgS%
(1) anode and cathode (1) , uksMvkS
j dS
FkksM
(2) no movement (2) dksbZxfr ugh
(3) both move towards cathode (3) nksuksdS
FkksMdhr ji Qt k; sxsa
(4) cathode and anode (4) dS
FkksMvkS
j , uksM
68. The point at which pH range of amino acid in 68. vehuksvEy dht y es apH js
a
t dkog fcUnqft l i j ; s
water, it exist in zwilter ion form and can't move TohVj vk; u ds: i es
afeyrsgSvkS
j xfrghu gks
r sgSfcUnqdks
point called : dgrsgS %
(1) Isoelectronic point (1) vkbl kb
sysDVªksfud fcUnq
(2) Isoelectric point (2) vkbl ksbysfDVªd fcUnq
(3) Isotectic point (3) vkbl ksVsfDVd fcUnq
(4) Isometric point (4) vkbl ksesfVªd fcUnq

69. Solution + conc. HNO3   yellow color solution 69. foy; u + l kUnzHNO3 
 ih
ykja
x] foy; u es
agS%
have :
(1) Xyw
d kst
(1) Glucose
(2) Fructose
(2) i zQ
DVkst
(3) Protein (3) i zksVhu
(4) Fat (4) ol k
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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021
70. When glucose oxidise with HIO4 the no. of moles 70. t c Xyw
d ks
t dksHIO4 }kjkvkDl hdr̀ fd; kt krkgSrkscuus
of formaldeh yde and fo rmic acid will be okysi Q
keZ
fYMgkbMo i Q
kfeZ
d vEy dseks yksdhl a[ ; kØe'k%
respectively : gks
xh%
(1) 1 & 5 (1) 1 & 5
(2) 1 & 3 (2) 1 & 3
(3) 5 & 1 (3) 5 & 1
(4) 3 & 1 (4) 3 & 1
71. Gluconic acid formed after oxidation of glucose 71. Xywd ks
t dsvkDl hdj.kl sXyw
fud vEy fuEu ds}kjkcus
xk%
with :
(1) VkW ysu vfHkdeZd
(1) Tollen reagent
(2) Br2 t y
(2) Br2 water
(3) i Qg
safya
x foy; u
(3) Fehling solution
(4) mi jksDr l Hkh
(4) All of these
O
O
NH
NH belong to the name : 72. lq
=k fuEu uke dksO;Dr djrkgS%
72. Structure N O
N O H
H
(1) fFk; kehu
(1) Thiamine
(2) ; wj kfl y
(2) Uracil
(3) l kbVks l hu
(3) Cytocine
(4) Fkkbfeu
(4) Thymine
73. Biuret test is not given by : 73. ckbZ
;wjs V Vs LV dkSu ughns
r kgS%
(1) proteins (1) i zksVhu
(2) carbohydrates (2) dkcz kg
skbMªsV
(3) polypeptides (3) i ksyhisIVkbM
(4) urea (4) ; fwj; k
74. Among the following compounds : 74. fuEu ; kS fxdksdk{kkjh; Øe gksxk%
NH2 NH2

i. ii. Et3N i. ii. Et3N

NO2 NO2 NO2 NO2

iii. iv. iii. iv.

NH2 NH2
NH2 NH2

the order of basicity is :

(1) iv > iii > ii > i
(1) iv > iii > ii > i
(2) ii > i > iii > iv
(2) ii > i > iii > iv
(3) iii > iv > ii > i
(3) iii > iv > ii > i
(4) i > iii > iv > ii (4) i > iii > iv > ii

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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021
75. Aniline and methylamine can be differentiated by: 75. , uh yhu o es
fFku , ehu dksi gpku l drsgS%
(1) diazotisation followed by coupling with phenol
(1) MkbZ
, t ksuhdj.kdsckn i Q
huksy l s; q
Xed cukdj
(2) reaction with chloroform and aqueous solution of
KOH (2) DyksjksiQ
keZo t yh; KOH l svfHkfØ; kdjds
(3) reaction with HNO2 (3) HNO2 l sfØ; kdjds
(4) none of the above (4) dksbZugh
X
76. CH3  CH2 C  N 
 CH3CH2 CHO , Here X is :
76.
X
CH3  CH2 C  N  CH3CH2 CHO , ; gkW
X gS%
(1) SnCl2/HCl/H2O, boil (1) SnCl2/HCl/H2O, boil
(2) H2/Pd – BaSO4 (2) H2/Pd – BaSO4
(3) LiAlH4/ether (3) LiAlH4/ether
+
(4) NaBH4/ether/H3O (4) NaBH4/ether/H3O+
77. Hydrolysis of cyanogen gives : 77. l k; uks
tsu dkt y vi ?kVu djusi j ns
r kgS%
(1) oxalic acid + NH3 (1) vkW
Dt sfyd vEy + NH3
(2) oxalic acid
(2) vkW
Dt fsyd vEy
(3) NH3
(3) NH3
(4) Acetic ccid
(4) , fl fVd vEy
78. Identify the end product in the given sequence of
reactions : 78. nhxbZvfHkfØ; kvks
adkvfUre mRikn D; kgks
xk%

(i) CH CN
NBS
 X M
g / ether

(i) CH CN
 Y (ii)H33 Z NBS
 X M
g / ether
  Y (ii)H33
O
Z
O

COCH3 CN COCH3 CN

(1) (2) (1) (2)

COOH COOH COCH3

COCH3
(3) (4) (3) (4)

79. An organic compound 'A' having molecular 79. , d dkcZ fud ;kSfxd 'A' dkv.kq lq
=kC2H3N gSft l dkvi p;u
formula C 2H 3N on reduction gives another djusi j nq l jk; kS
fxd 'B' i zkIr gks
r kgSB dkukbVªl vEy ds
compound 'B'. Upon treatment with nitrous acid l kFkfØ;kdjkusi j , fFky , Ydks gky nsr kgSAft l dksDyks
jks
iQkeZ
'B' gives eth yl al coho l. On warming w ith
chloroform and alcoholic KOH, it forms an vkS j , Ydks
gkfyd KOH dsl kFkxeZdjusi j ; kS fxd 'C' dh
offensive semelling compound 'C'. The compound rh{k.kxa / nsr kgSA; kSfxd 'C' gS%
'C' is : (1) CH3NC
(1) CH3NC
(2) C6H5NC
(2) C6H5NC
(3) CH3C  N
(3) CH3C  N
(4) CH3CH2NC (4) CH3CH2NC
80. Compare boiling point of isomeric alkyl amines : 80. fuEu vkbl ks
es
fjd , fYdy , ehuksdsDoFkuka
d dkl ghØe gS
:
(1) 10 > 20 > 30 (1) 10 > 20 > 30
(2) 10 > 20 < 30 (2) 10 > 20 < 30
(3) 10 < 20 < 30 (3) 10 < 20 < 30
(4) 10 < 20 > 30
(4) 10 < 20 > 30
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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021
81. Acetamide is treated with the following reagents 81. , l h vkekbMdksfofHkUu vfHkdeZ d dsl kFkfØ; kdjkusi j]
separately. Which one of these would yield methyl
amine :
fuEu es al sfdl l ses
fFky , ehu i zkIr gks
xk%
(1) PCl5 (1) PCl5
(2) NaOH/Br2
(2) NaOH/Br2
(3) Sodalime (3) l kM
skykbe
(4) Hot conc. H2SO4 (4) xeZr Fkkl kUnzH2SO4
HNO2 PCl3 NH3
82. C2H5NH2   A   B   C . Recognize the 82. HNO2
C2H5NH2  PCl3
 A  NH3
 B   C . ; kS
fxd 'C' gks
xk%
compound C from the following :
(1) i zkissuukbZ
Vªkby
(1) propanenitrile
(2) esfFky, ehu
(2) methylamine
(3) , fFky , ehu
(3) ethylamine
(4) acetamide (4) , fl VkekbM
83. Identify the product (E) in the following sequence 83. fuEu vfHkfØ; kes
al smRikn (E) dhi gpku dfj; s%
of reactions :
CH3
CH3 Br2 Sn /HCl NaNO2 /HCl H2 O/H3PO2 KMnO4
  A   B 
273278 K
 C  D 
OH
E
Br2 Sn /HCl NaNO2 /HCl H2 O/H3PO2 KMnO4
  A   B 
273278 K
 C  D 
OH
E
NO2
NO2
COOH
COOH
(1)
(1)

COOH
COOH Br
Br (2)
(2)

CH3
CH3 (3)
(3) Br
Br
CH3
CH3 (4)
(4) O 2N Br
O 2N Br
– +
OH O Na
OH
–
O Na
+ 84. CHCl3  NaOH 
84. CHCl3  NaOH  CHO
CHO
mi jks
Dr vfHkfØ; kes
ai z;q
Dr bys
DVªks
iQkby gks
xk%
The electrophilie involved in the above reaction
is : (1) VªkbZ
esa

fFky , uk; u(CCl3 )

(1) trichloromethyl anion (CCl3 ) 
(2) iQ
kfeZ
y dsVk; u(CHO)

(2) formyl cation (CHO) 
(3) MkbZ
DyksjksesfFky dsVk; u(CHCl2 )

(3) dichloromethyl cation (CHCl2 ) (4) MkbZ
Dyksjkd
s kchu
Z(:CCl2)
(4) dichlorocarbene (:CCl2)

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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021
 
H2 O HCN H2 O / H H2 O HCN H2 O / H
85. CH  CH 
Hg2 H

CN excess
   ........ T he 85. CH  CH 
Hg2 H

CN excess
   ........ v fUr e
final product is : mRikn gks
xk%
O O
(1) CH3  C  NH2 (1) CH3  C  NH2
(2) CH3–CH2–COOH (2) CH3–CH2–COOH

(3) CH3  CH  CH3 (3) CH3  CH  CH3

CN CN
H H
(4) CH3  C  COOH (4) CH3  C  COOH
OH OH
86. Which one of the following statements about
CH3CN is not true :
86. fuEu es
al sdkS
u l kdFku CH3CN dsckjses
al ghughgS%
(1) Its IUPAC name is ethanenitrile (1) bl dkIUPAC uke , FksuukbVkby gS
(2) The bond between C and N is a triple bond (2) C vkjSN dschp f=kcU/ gksrkgS
(3) The C–C–N bond angle is 1800. (3) C–C–N dschp 1800 gS
(4) The carbon-carbon bond is shorter than the carbon-
nitrogen bond. (4) dkcZ
u&dkcZ
u cU/ dkcZ
u ukbZ
Vªkst u cU/ l sNksVkgkrskgS
i.NH3 NaNO2 NaOI
87. A i.NH3 NaNO2
 B  NaOI
 C  CH3COONa  CHI3 87. A   B 
ii.H2 /Ni HCl
 C  CH3COONa  CHI3
ii.H2 /Ni HCl

Recognize the compound A from the following : ; kS

fxd 'A' gks
xk%
(1) CH3CHO ((1) CH3CHO
(2) CH3CH2OH (2) CH3CH2OH
(3) CH3COCH3 (3) CH3COCH3
(4) CH3COOH (4) CH3COOH
88. Arrange the following in decreasing order of their
Pkb values : 88. fuEu dksmudsPkb eku ds?kVrsØe es
afy[ kks
a%
A. C6H5NH2 B. C2H5NH2 A. C6H5NH2 B. C2H5NH2
C. (C2H5)2NH D. NH3 C. (C2H5)2NH D. NH3
(1) A > D > C > B (1) A > D > C > B
(2) A > D > B > C (2) A > D > B > C
(3) B < C < D < A (3) B < C < D < A
(4) C > B > D > A (4) C > B > D > A
89. Among the following compounds, the most basic 89. fuEu ; kS
fxdks
aes
a
] l cl svf/ d {kkjh; dkS
u l kgS%
compound is :
(1) (2)
(1) (2)

(3) (4)
(3) (4)

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 All India Test and Discussion Series : Test-27 / [Paper] CRACK NEET 2021 / TD / 28 -May-2021
NO2 NO2
Zn /NH4 Cl Sn / HCl Zn /NH4 Cl Sn / HCl
90. Y    X 90. Y    X

X and Y are : X o Y gS%

(1) aniline, phenyl hydroxylamine (1) , uhyhu] i Q fsuy gkbMkªD Wl hy,ehu
(2) phenyl hydroxylamine, aniline (2) iQfsuy gkbMkªD Wl hy, ehu, , uhyhu
(3) aniline and hydrobenzene (3) , uhyhu vkjSgkbM kªcsU
st hu
(4) hydrobenzene and aniline (4) gkbM kªcsU
st hu vkjS, uhyhu

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