ETHER

Total No.of questions in Ether are -

Level # 1 ................................................................................... 25
Level # 2 ........................................ ........................................ 25
Level # 3 ........................................ ........................................ 33
Level # 4 ........................................ ........................................ 05

Total No. of questions ............................................................. 88

 LEVEL # 1
Questions
based on Introduction Q.8 In order to obtain diethyl ether from ethanol,
the latter is taken in -
Q.1 The number of alkanols and ethers represented (A) In equal amount of sulphuric acid
by the molecular formulae C3H8O and C4H10O
(B) In slightly lesser amount of sulphuric acid
respectively are given by the set-
(A) 2 , 1 ; 3 , 2 (B) 1, 2 ; 2 , 3 (C) In excess amount of sulphuric acid
(C) 2 , 1 ; 4 , 3 (D) 2 , 1 ; 3 , 4 (D) In far lesser amount of sulphuric acid

Q.2 Which is mismatched - Q.9 For making (CH 3) 3 C–O–C 2H 5 the ideal
combination is -
(A) C2H5–O–C2H5
(A) (CH3)3CONa and C2H5Br
Four primary carbon atoms
(B) CH3–CH2–CH(OH)CH3 (B) (CH3)3CBr and C2H5ONa
Optically active (C) Both the above
(C) CH3–O–CH (CH3)2 (D) None
Two secondary carbon atoms
Q.10 Mixed ether will not be formed in the reaction-
(D) Ether is heated with CH3COCl in presence
of AlCl3 CH3COOC2H5 + C2H5Cl (A) CH3OCH2Cl + C2H5MgBr
(B) CH2N2 + C2H5OH
Q.3 Diethyl ether is metamer of - (C) C2H5ONa + CH3I
(A) Ethoxyethane (D) C2H5OH + H2SO 4 (140ºC)
(B) Methyl propyl ether
(C) Methoxyethane Q.11 In which case ether is formed -
(D) Ethoxymethane
(A) (CH3)3C–Br + CN
Q.4 Anhydrides of alcohol are nothing but - (B) CH3CH2Br + (CH3)3 CO 
(A) Ethers (B) Aldehydes
(C) Esters (D) Alkyl anhydrides (C) (CH3)3 C–Cl + OC2 H5
(D) None of the above
Q.5 Electron pair donating tendency is maximum
in - Questions
(A) Me–O–H (B) Me–O–Me based on Physical properties
(C) Et–O–H (D) Et–O–Et
Q.12 Diethyl ether acts as a -
Q.6 Which of the following is a cyclic ether- (A) Lewis acid
(A) Ethyl ether (B) Vinyl ether (B) Lewis base
(C) Phenyl ether (D) Tetrahydrofurane (C) Reducing agent
Questions
(D) Oxidising agent
based on Method of preparation
Q.7 In which case the product is neither a cyclic Q.13 Ethers like alcohols do not form strong.....
ether nor open chain symmetrical ether- bonding . Hence they are more volatile -
(A) Covalent
(A) CH3– CH = CH – CH3  C
6H5 CO 3H

(B) Hydrogen
(B) CH3CH2ONa + C2H5Br 
(C) Coordinate
(C) KCN + (CH3)3 CBr 
(D) None of the above
(D) C2H5OH (Excess) + H2SO 4 140º

 Questions Q.19 Ether on carbonylation gives -
based on Chemical Properties
(A) Alkanoic acid (B) Alkanone
Q.14 The compound obtained by the reaction of (C) Alkyl alkanoate (D) Alkanal
diethyl ether with chlorine in the presence of
sun light, is - Q.20 First member of ether series on reaction with
(A) Perchloro diethyl ether sodium and liquified ammonia gives -
H5C2–OC2Cl 5 (A) Methanol + methane
(B) Perchloro diethyl ether (B) Ethane+ methanol
Cl5C2–O–C2Cl 5 (C) Ethanol
(D) Ethane
(C)  ,  ' - Dichloro diethyl ether
ClCH2CH2–O–CH2CH2Cl Q.21 Which of the following compounds forms an
adduct with diethyl ether through coordinate
(D)  ,  ' - Dichlorodiethylether bond -
CH3  CH  O  CH  CH3 (A) BF 3 (B) Oxygen of air
| | (C) HCl gas (D) All of the above
Cl Cl
Q.22 Which of the following is a false statement -
Q.15 Diethyl ether absorbs oxygen to form -
(A) Diethyl ether gives ethyl iodide on reacting
(A) Red coloured sweet smelling compound with HI
(B) Acetic acid
(B) Diethyl ether and methyl isopropyl ether
(C) Ether sub oxide are chain isomers
(D) Ether peroxide (C) Diethyl ether is a Lewis base
Q.16 Diethyl ether and air giv es ether- (D) Diethyl ether hydrolyses to ethanol by
hydroperoxide. The mechanism of the dil.H2SO 4
reaction is -
Q.23 Mark the correct statement -
(A) Nucleophilic substitution
(A) Ethers behave as Lewis base
(B) Free radical addition
(B) Ethers form coordination complexes with
(C) Free radical substitution Lewis acids
(D) None of the above (C) With cold HI diethyl ether gives ethyl
alcohol & ethyl iodide
Q.17 The order of reactivity of halogen acids with
ether is - (D) All are correct
(A) HCl > HBr > HI (B) HI > HBr > HCl Q.24 Ethers are quite stable towards -
(C) HCl > HI > HBr (D) HI > HCl > HBr (A) Oxidising agents (B) Reducing agents
(C) Na metal (D) Bases
Q.18 The reaction of ethoxyethane and ethanoyl
chloride is carried out in presence of Q.25 Ether is used as -
anhydrous aluminium chloride. The product
(A) An antiseptic and a solvent
on alkaline hydrolysis gives -
(B) An anaesthetic and a solvent
(A) CH3CH2OH
(B) CH3CH2OCH2CH3 (C) A fire extinguisher under the trade name
pyrene
(C) CH3OCH3
(D) A dry cleaning solvent
(D) CH2 CH2
O
 LEVEL # 2
Q.1 Ether in contact with air for a long time form Q.7 Ether is not formed in this reaction -
peroxides. The presence of peroxide in ether Conc. H SO
(A) 2C2H5OH    
2 4
can be tested by adding Fe2+ ion in it and 140 º
then adding -
(B) (CH3)3 C–Cl + C2H5ONa 
(A) KCNS (B) SnCl 2
(C) C2H5Cl + (CH3)3 C–ONa 
(C) HgCl2 (D) KI
(D) Oxygen of ether can be replaced by
Q.2 Match list I with list II and then select the chlorine when treated with PCl5
correct answer from the codes given below
the lists - Q.8 Unsymmetrical ethers are best prepared by -
List I
(A) Willamson's continuous etherification
(A) (CH3)3C — OH
process
(B) CH3 — O — C (CH3)3
(B) Reacting Grignard reagent with alkyl
(C) C2H5 — O — C2H5
halide
(D) CH3 — O — CH (CH3)2
(C) Treating sodium alkoxides with alkyl
List II bromides
(a) Sulphuric ether (D) Heating an alkanol with conc. H2SO 4
(b) Chain isomer of 1-butanol
(c) Mixed ether Q.9 Which of the following is used as an additive
(d) Has one secondary carbon by fire departments under the name Rapid-
Water -
Codes :
A B C D (A) Ethylene glycol
(A) b d a c (B) Polyethylene oxide
(B) b c a d (C) Epichlorohydrin
(C) b c d a (D) Epoxy oxide
(D) c b a d
Q.10 In the Williamson's synthesis for diethyl ether,
Q.3 Ether reacts with chlorine in the dark to form- which species works as a nucleophile -
(A) CH2Cl — CH2 — O — CH2 — CH3 (A) Halide ion (B) Ethoxide ion
(B) CH2Cl — CH2 — O — CH2 — CH2Cl (C) Ethyde ion (D) Hydride ion
(C) CH3 — CH (Cl) — O — CH(Cl) — CH3
(D) CCl3 — CH2 — O — CH2 — CCl 3 Q.11 The structure of the compounds formed by
the reaction of diethyl ether with oxygen of
Q.4 Ether does not form oxonium salt on reaction air is -
with -
(A) CH3CH2 – O – O – CH2CH3
(A) Cold conc. H2SO 4
(B) Cold conc. HCl CH3
(C) Conc. HI |
(D) None of the above (B) CH3CH2 – O – CH  O – O – H
(C) CH3CH2 – O – O – CH2 – O – CH3
Q.5 The ordinary alkyl ethers are cleaved by - (D) CH2 (OCH3) – CH2 – O – C2H5
(A) Ethanol (B) Ethyl halide
(C) BF 3 (D) Hydrogen iodide Q.12 Ether bottles should not be kept open in air
because -
Q.6 The decomposition of ethers by HI or HBr is
called - (A) Ether is an anaesthetic
(A) Zerewitinoff's reaction (B) Ether forms an explosive peroxide
(B) Ziesel's method (C) Ether is costly
(C) Williamson's method (D) Ether gets oxidised to ethanol
(D) Hell-Volhard-Zelinsky reaction
Q.13 Isopropyl alcohol vapour is passed over Q.17 The ether C6H5OCH2C6H5 on heating with
alumina heated at about at about 240ºC. The concentrated HI produces -
product formed is - (A) C6H5I and C6H5CH2OH
(A) diisopropyl ether (B) C6H5I and C6H5CH2I
(C) C6H5OH and C6H5CH2I
(B) propene
(D) C6H5OH and C6H5CH2OH
(C) a mixture of diisopropyl ether and propene
(D) 3-hexene Q.18 Consider the following transformation.
con.HI
Q.14 Which of the following is not expected to CH3CH = CH – O – CH2CH3  
heat
giv e ether on reaction with sodium The major product(s) formed is (are) -
methoxide - (A) CH3CH = CHI and CH3CH2I
(A) CH3CH2CH2Cl (B) CH3CH = CHI and CH3CH2OH
(B) CH2 = CHCH2Cl (C) CH3CH2CHO and CH3CH2I
(C) PhCH2Cl (D)
(D) CH2 = CHCl

Q.15 Consider the following reaction, Q.19 Ethyl methyl ether on heating with PCl 5
1. (CH COO) Hg,CH OH
produces -
CH3CH = CH2  3 
2
 3 (A) ethyl chloride and methyl alcohol
2.NaBH 4
(B) acetyl chloride and methyl chloride
The product formed in the reaction is - (C) ethylidene dichloride and methylene
dichloride
(D) ethyl chloride and methyl chloride
(A)
Q.20 The reaction C2H5OC2H5 + 2HI  heat

2C2H5I + H2O involves the mechanism -
(B) (A) SN1 (B) SN2
(C) E1 (D) E2
(C)
Q.21 Propene is allowed to react with HI.The
product (A) is then treated with CH3ONa to
give a new product (B).
(D) HI
CH3CH = CH2   A CH ONa
3 B
The structure of the product (B) is -
Q.16 Dimethyl ether, Me2O, is highly soluble in (A) CH3CH2CH2OCH3
water while diethyl ether, Et 2O, is only
sparingly soluble because -
(B)
(A) Me2O reacts with water efficiently due to
its small sized methyl groups but Et2O (C) CH3CH2OCH2CH3
does not (D) CH3CH2OCH=CH2
(B) hydrogen bonding between Et2O and H2O
is less efficient due to steric crowding Q.22 In the reaction
around oxygen of Et2O while the hydrogen NBS
C H5ONa
CH3CH = CH2  A 2   B
bonding between Me2O and H2O is much CCl4
efficient due to small size of the methyl the product (B) is -
groups
(C) C2H5 – groups has a stronger +I effect
than CH3 – group (A)
(D) hyperconjugation of C – H bond is greater (B) CH2=CHCH2OC2H5
in Me2O than in Et2O (C) CH3CH2CH2OC2H5
(D) C2H5CH2OCH=CH2
Q.23 One mole of t-butyl methyl ether on being Q.25 Which one among the following reactions is
heated with 1 mole of concentrated hydriodic an example of Williamson synthesis -
acid gives -
Zn–Hg
(A) CH3OH (1 mole) and (CH3)3CI (1 mole) (A) CH3COCH3   CH3CH2CH3
Conc.HCl,heat
(B) CH3I (1 mole) and (CH3)3COH (1 mole)
(C) CH3I (1 mole) and (CH3)3CI (1 mole) 1. dil NaOH,heat
(B) CH3CHO    
(D) CH3OH (1 mole) and (CH3)3COH (1 mole) 2.H3 O , heat

CH3CH=CHCHO
Q.24 Which of the following reactions does not
heat
yield an alkyl halide? 
(C) C2H5I + C2H5ONa  C2H5OC2H5
2 Cl heat
(A) CH3CH2OCH2CH3 
hv
 
(D) HCHO+NaOH  HCOONa + CH3OH

conc .HI
(B) CH3CH2OCH2CH3  
heat

5 PCl
(C) CH3CH2OCH2CH3  
heat

2 SOCl
(D) CH3CH2OH 
 
 LEVEL # 3
Q.1 The systematic name of the compound
Q.5 In the reaction

is Al2O3
2C2H5OH   (C2H5)2 O + H2O
240 º C
(A) 2-methyl 2--(1 methylethoxy)propane
(B) t-butyl isopropyl ether alumina acts mainly as

(C) 1-isopropoxy-1,1-dimethylethane (A) an absorbent of water

(D) 2-(1, 1-dimethylethoxy)propane (B) a provider of hot solid surface
(C) a Lewis acid to coordinate (C2H5)2O formed
Q.2 The ether in which all atoms may exist in one
plane is (D) a Lewis acid catalyst to increase the leaving
group ability of the —OH group by coordination
(A) (B) at oxygen.

Q.6 Di-t-butyl ether is prepared best by the reaction

(C) (D)

(A) (CH3)3C — Br + (CH3)3COK 

Q.3 The reaction
conc .H SO
2 
4 H2SO 4
2C2H5OH    (C2H5)2 O + H2O (B) (CH3)3 C — OH  
140 º C 140 º C

is an example of
2 3 Al O
(A) an elimination reaction (E2) (C) (CH3)3 C — OH  
240 º C
(B) an electrophilic substitution (SE2) reaction
conc .
33  (CH ) COH
(C) a nucleophilic substitution (SN1) reaction (D) (CH3)3C=CH2 HSO

   
2 4
(D) a nucleophilic substitution (SN2) reaction

Q.4 Pinacol vapour is passed over alumina heated Q.7 Reaction of t-butyl bromide with sodium
at about 350ºC. methoxide produces
CH3 CH3 (A) isobutane (B) isobutylene
| | (C) sodium t-butoxide
CH3  C — C  CH3
| | (D) t-butyl methyl ether
OH OH
Q.8 Which of the following reactions would give
The major product formed in the reaction is:
the best yield of t-butyl methyl ether ?
(A) CH3COC(CH3)3

CH3 CH3 2 4 H SO
(A) (CH3)3 C — OH  
| | 140 º C
(B) CH2  C — C  CH2
(B) (CH3)3 C — Br + CH3OH 
(C) (CH3 )2 C — C (CH3 )2
(C) (CH3)3 C — Br CH3ONa 

(D) (CH3)2 CHOCH(CH3)2 (D) (CH3)3 C — OK + CH3Br 

Q.9 In the reaction Q.12 Aleksandar Butlerov carried out the following
reaction in 1861.
THF
CH3CH2ONa + CH3CH2OSO2CH3   100 ºC
heat CH3CHCOOH  HI  

H2O
the product formed is |
OC2H5
(A) CH3CH2OCH3
(B)CH3CH2OCH2CH3 The products obtained by him were
(A) -iodopropionic acid and ethyl alcohol
(C) CH3CH2OSO2OCH2CH3 (B) -iodopropionic acid and ethyl iodide
(C) lactic acid and ethyl iodide
(D) CH3CH2OSO2OCH3 (D) lactic acid and ethyl alcohol

Q.13 In the reaction

Q.10 1-Chloro-2-butene is allowed to react with a heat
(CH3)3 C — O — CH2CH3 + HI 
concentrated solution of C2H5ONa in C2H5OH (1mole)
The rate of reaction is found to be dependent the product(s) formed is (are)
on the concentrations of both the substrate (A) (CH3)3 C—OH and CH3CH2I
and the nucleophile. (B) (CH3)3 C— I and CH3CH2OH
(C) (CH3)3 C— I and CH3CH2I
C2H5OH
CH3CH = CHCH2Cl + C2H5ONa  
 
(D) (CH3 )3 C — O — CH2 CH3 I 
The major product formed in the reaction is |
H
(A) CH3CH = CHCH2OC2H5
Q.14 In the reaction
(B) CH3 CH — CH  CH2
|
OC2H5
the product (A) has the structure

CH3
(C) CH2 = CH – CH = CH2
|
(D) All of these in equal amounts (A) CH3 — C — CH2OH
|
18
OH
Q.11 Identify the final product (B)in the following
CH3
sequence of reactions.
|
18
(B) CH3 — C — CH OH
2
CH3 |
| conc .H2SO 4 C H OH OH
CH3 — C  CH2     A 25 
 B
0 ºC
CH3
(A) (CH3)2 C —OSO3H |
(C) CH3 — C — CH3
(B) C2H5OC2H5 |
18
OH
(C) (CH3)3COC2H5 CH3
|
(D) (CH3)2CHCH2OC2H5
(D) CH3 — CH — CH218 OH
Q.15 Which of the following is known by the name Passage : (Qus. 20 to 22 )
epichlorohydrin ? Alexander Williamson prepared diethyl ether
(A) 3-Chloropropane by a simple method, now called as
(B) 3-Chloro-1-propanol Williamson’s ether synthesis. In this method
(C) 3-Chloro-1, 2-epoxypropane
an alkyl halide is treated with sodium alkoxied
(D) None of these
prepared from sodium and alcohol.
Q.16 Diethyl ether on being exposed to air for a – –
R—O + R' — x  R—O—R' + x
long time forms some amount of diethyl ether
hydroperoxide. the presence of this This reaction is used in the synthesis of
hydroperoxide compound in diethyl ether can symmetrical and unsymmetrical ethers.
be detected by adding ferrous sulphate into it
It may be noted that f or preparing
and then adding
(A) KCNS (B) SnCl2 (C) HgCl2 (D) KI unsymmetrical ethers, the halide used should
preferably be primary because secondary and
Q.17 Which of the following reactions will not result tertiary alkyl halides may form alkenes as
in the formation of anisole ? major product due to elimination process.
CH3
(A)
CH3–C–Br +Na +O –—C2H5 
(B) Sodium
CH3 ethoxide
CH3
(C)
CH3–C=CH2 + C2H5OH + NaBr
2-methyl propene
(D)
Aryl ethers or phenolic ethers can be prepared
by using sodium phenoxide and alkyl halides.
Q.18 2-Phenylethanol may be prepared by the However, aryl halides and solium alkoxide
reaction of phenylmagnesium bromide with cannot be used for preparing phenolic ethers
(A) HCHO (B) CH3CHO because aryl halides are less reactive towards
nucleophilic substitution reactions.
(C) CH3COCH3 (D) Answer the following questions :

Q.20 Arrange the following halides in decreasing

Hg(OAc )2
Q.19    NaBH4 order of reactivity towards Williamson’s ether
CH3OH    A, A, is:
synthesis :
CH3CH2CH2Cl (u) CH3CH2CH2Br (v)
(A)
(CH3)3 C–CH2Br (w) CH2 = CH —CH2Cl(x)
(A) (x) > (v) > (u) > (w)
(B) (B) (u) > (v) > (w) > (x)
(C) (w) > (x) > (v) > (u)
(C)
(D) (v) > (w) > (x) > (u)

(D)
Q.21 Methyl tertiary butyl ether (MTBE) is added in Statement Based Questions
gasoline to improve its octane number. Each of the questions given below consist
of Statement – I and Statement – II. Use the
CH3 following Key to choose the appropriate
CH3–C–O–CH3 answer.
(A) If both Statement- I and Statement- II are
CH3
true, and Statement - II is the correct
explanation of Statement– I.
Which of the following is the best method for (B) If both Statement - I and Statement - II
synthesis of the above ether ? are true but Statement - II is not the
(A) (CH3)2C= CH2 + CH3OH H2SO correct explanation of Statement – I.

4 
(C) If Statement - I is true but Statement - II
(B) (CH3)3CBr + CH3ONa 
 is false.
(D) If Statement - I is false but Statement - II
(C) (CH3)3C – O– – Na+ + CH3I 
 is true.

(D) All of these reactions

Q.28 Statement I : Ether behaves as bases in the
presence of mineral acids.
Q.22 To which of the following mechanisms does
the reaction (Williamson’s ether synthesis) Statement II : Due to the presence of lone
pair of electrons on oxygen.
belong ?
(A) SN1 (B) SN2 Q.29 Statement I : The boiling point of ethanol is
(C) E1 (D) E2 much higher than that of dimethyl ether.
Statement II : In ethanol, the molecules are
True/False type Questions associated by the formation of intermolecular
hydrogen bonding whereas in diethyl dether it
Q.23 The presence of peroxide in ether can be is absent.
tested by development of red colour when ether
Q.30 Statement I : Tert. butyl methyl ether is not
is shaken by a mixture of ferrous sulphate prepared by the reaction of tert. butyl bromide
and KCNS. with sodium methoxide.
Statement II : Sodium methoxide is a strong
Q.24 Diethyl ether in presence of BF3 combines nucleophile.
with CO at 150ºC and 500 atmospheric
pressure and forms ethyl propionate. Q.31 Statement I : W ith HI, anisole f orms
iodobenzene and methyl alcohol.
Q.25 Diethyl ether and 1-butanol have the same
solubility in water. Statement II : I ion will combine with smaller
group to avoid steric hindrance.
Q.26 Williamson’s synthesis of ethers is an example Q.32 Statement I : Tert. butyl methyl ether on
of nucleophilic substitution reaction. cleavage with HI at 373 K gives tert. butyl iodide
and methanol.
Q.27 Coordination complexes of ethers with Lewis
Statement II : The reaction occurs by SN2
acids are called etherates.
mechanism.
Q.33 Match the following :
Column – I Column – II
(1) Diethyl ether (A) Epoxide
(2) Williamson’s (B) Unsymmetrical
synthesis ether
(3) Zeisel’s method (C) Anaesthetic
(4) ROR’ (D) Mixture of alcohol
and ether

(5) CH3–CH–CH2 (E) Ether + solid CO2

(6) Natalite (F) Ethoxy ethane

(7) Halothane (G) Estimation of
alkoxy group
(8) Cooling material (H)C2H5ONa+C2H5Br
(9) Phenetole (I) Coordinate
complexes
(10) Etherates (J) Ethoxy bezene
 LEVEL # 4
(Questions asked in previous AIEEE & IIT-JEE)

SECTION-A
SECTION-B
Q.1 HBr reacts with CH2 = CH – OCH3 under anhy-
Q.1 Benzenediazonium chloride on reaction with
drous conditions at room temperature to give-
phenol in weakly basic medium gives –
(A) BrCH2CHO and CH3OH
(A) Diphenyl ether
(B) BrCH2 – CH2 – OCH3
(B) p-hydoroxyazobenzene
(C) H3C – CHBr – OCH3
(C) Chlorobenzene
(D) CH3CHO and CH3Br
(D) Benzene

OH O–Na+
Q.2 + CHCl3 + NaOH . Q.2 The ether –O–CH2 – when treated
CHO
with HI produces
The electrophile involved in the above reaction
is : (A) –CH2I (B) –CH2OH
(A) dichlorocarbene ( :CCl2)
Θ (C) –I (D) –OH
(B) trichloromethyl anion ( CCl3 )


(C) formyl cation ( CHO )


(D) dichloromethyl cation ( CHCl2 )

Q.3 In the following sequence of reactions,

P  I2 Mg HCHO
CH3CH2OH   A  B  

ether
2H O
C  D, then compound ‘D’ is –

(A) butanal
(B) n-butyl
alcohol
(C) n-propyl alcohol
(D) propanal
 ANSWER KEY
LEVEL # 1

Ques. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15
Ans. C C B A D D C C A D B B B B D
Ques. 16 17 18 19 20 21 22 23 24 25
Ans. B B A C A D B D C B

LEVEL # 2

Qus. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15
Ans. A B C C D B B C B B B B C D B
Qus. 16 17 18 19 20 21 22 23 24 25
Ans. B C C D B B B A A C

LEVEL # 3
Ques. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15
Ans. A B D B D D B D B A C C B A C
Ques. 16 17 18 19 20 21 22
Ans. A D D D A C B

Ques. 23 24 25 26 27
Ans. TRUE TRUE FALSE TRUE TRUE

Ques. 28 29 30 31 32
Ans. A A B D C

Ques. 33

Ans. 1–F, 2–H, 3–G, 4–B, 5–A, 6–D, 7–C, 8–E, 9–J, 10–I

LEVEL # 4
SECTION -A
Ques. 1 2 3
Ans. D A C

SECTION -B
Ques. 1 2
Ans. B A,D