Explore topic-wise MCQs in Joint Entrance Exam - Main (JEE Main).

This section includes 11242 Mcqs, each offering curated multiple-choice questions to sharpen your Joint Entrance Exam - Main (JEE Main) knowledge and support exam preparation. Choose a topic below to get started.

7151.

Froth floatation process is used for concentration of [MNR 1987; IIT 1989; UPSEAT 2000, 02]

A. Chalcopyrite
B. Bauxite
C. Haematite
D. Calamine
Answer» B. Bauxite
7152.

'Lapis-Lazuli' is a blue coloured precious  stone. It is mineral of the class [NCERT 1980; AIIMS 1980; BHU 1978, 80]

A. Sodium-alumino silicate
B. Zinc cobaltate
C. Basic copper carbonate
D. Prussian blue
Answer» B. Zinc cobaltate
7153.

Which is correct [MADT Bihar 1995]

A. Galena : \[M{{g}_{2}}C{{O}_{3}}\]
B. Cassiterite : \[CaC{{O}_{3}}\,MgC{{O}_{3}}\]
C. Dolomite : \[Sn{{O}_{2}}\]
D. Magnesite : \[MgC{{O}_{3}}\]
Answer» E.
7154.

Black Jack is an ore of [PCET 2004]

A. Cr
B. Sn
C. Zn
D. Ni
Answer» D. Ni
7155.

Which one of the following can be used as monomer in a polymerisation reaction            [MP PMT 1993]

A.                 \[C{{H}_{3}}C{{H}_{2}}Cl\]           
B.                 \[C{{H}_{3}}C{{H}_{2}}OH\]
C.                 \[{{C}_{6}}{{H}_{6}}\]    
D.                 \[{{C}_{3}}{{H}_{6}}\]
Answer» E.
7156.

Styrene at room temparature is

A.                 Solid     
B.                 Liquid
C.                 Gas       
D.                 Colloidal solution
Answer» C.                 Gas       
7157.

Perlon is                                               [AFMC 2001]

A.                 Rubber                
B.                 Nylon-6
C.                 Terelene             
D.                 Oxlon
Answer» C.                 Terelene             
7158.

High density polyethylene (HDPE) can be prepared from ethylene by

A.                 Ziegler-Natta process
B.                 Heating with peroxides
C.                 Condensing in sealed tubes
D.                 Condensing with styrenes
Answer» B.                 Heating with peroxides
7159.

In the manufacture of polythene by the Ziegler process using ethylene, the temperature for proper polymerisation required is

A.                 Below \[{{10}^{o}}C\]
B.                 \[{{10}^{o}}\text{ to }{{50}^{o}}C\]
C.                 \[{{50}^{o}}\text{ to }{{80}^{o}}C\]         
D.                 \[{{80}^{o}}\text{ to }{{140}^{o}}C\]
Answer» D.                 \[{{80}^{o}}\text{ to }{{140}^{o}}C\]
7160.

Polymer used in bullet proof glass is        [MP PET 2004]

A.                 Lexane
B.                 PMMA
C.                 Nomex
D.                 Kevlar
Answer» C.                 Nomex
7161.

Ebonite is                                            [CBSE PMT 2000]

A.                 Polropene          
B.                 Natural rubber
C.                 Synthetic rubber             
D.                 Highly vulcanized rubber
Answer» E.
7162.

?Celanese silk? is

A.                 Cellulose trinitrate          
B.                 Cellulose acetate
C.                 Cellophane        
D.                 Pyroxylin
Answer» C.                 Cellophane        
7163.

Which of the following is a chain growth polymer [CBSE PMT 2004]

A.                 Polystyrene       
B.                 Protein
C.                 Starch  
D.                 Nucleic acid
Answer» B.                 Protein
7164.

Which of the following statement is correct regarding the drawbacks of raw rubber         [AIIMS 2001]

A.                 It is plastic in nature
B.                 It has little durability
C.                 It has large water-absorption capacity
D.                 All of these
Answer» E.
7165.

Wash and wear clothes are manufactured using

A.                 Nylon fibres      
B.                 Cotton mixed with nylon
C.                 Terylene fibres
D.                 Wool fibres
Answer» D.                 Wool fibres
7166.

Trans-form of polyisoprene is

A.                 Guttapercha     
B.                 Hydrochloride rubber
C.                 Buna-N
D.                 Synthetic rubber
Answer» B.                 Hydrochloride rubber
7167.

p-chloroaniline and anilinium hydrochloride can be distinguished by                                        [IIT-JEE 1998]

A.                 Sandmeyer reaction      
B.                 \[NaHC{{O}_{3}}\]
C.                 \[AgN{{O}_{3}}\]             
D.                 Carbylamine test
Answer» C.                 \[AgN{{O}_{3}}\]             
7168.

Aniline reacts with  acetaldehyde to form [MHCET 2004; AFMC 2004]

A.                 Schiff's base      
B.                 Carbylamine
C.                 Immine               
D.                 None of these
Answer» B.                 Carbylamine
7169.

Which of the following would be most reactive towards nitration              [AMU 2000; UPSEAT 2002]

A.                 Benzene             
B.                 Nitro benzene
C.                 Toluene              
D.                 Chloro benzene
Answer» C.                 Toluene              
7170.

The correct order of basicity?s of the following compounds is \[\underset{4}{\mathop{C{{H}_{3}}-\overset{O}{\mathop{\overset{||}{\mathop{C}}\,}}\,-N{{H}_{2}}}}\,\]                        [IIT-JEE (Screening) 2001]

A.                 \[2>1>3>4\]      
B.                 \[1>3>2>4\]
C.                 \[3>1>2>4\]      
D.                 \[1>2>3>4\]
Answer» C.                 \[3>1>2>4\]      
7171.

The following compound on hydrolysis in aqueous acetone will give

A.                 Mixture of (K) and (L)   
B.                 Mixture of (K) and (M)
C.                 Only (M)
D.                 Only (K)
Answer» B.                 Mixture of (K) and (M)
7172.

Which of the following is the strongest base ?    [AIEEE 2004]

A.                
B.                
C.                                     
D.                
Answer» E.
7173.

The structural formula of Indigo dye is : [DPMT 2004]

A.                
B.                
C.                
D.                
Answer» D.                
7174.

Aniline when diazotized in cold and then treated with dimethyl aniline gives a coloured product. Its structure would be                                 [CBSE PMT 2004]

A.                
B.                
C.                
D.                
Answer» B.                
7175.

A primary amine is formed an amide by the treatment of bromine and alkali. The primary amine has :     [BHU 2004]

A.                 1 carbon atom less than amide
B.                 1 carbon atom more than amide
C.                 1 hydrogen atom less than amide
D.                 1 hydrogen atom more than amide
Answer» B.                 1 carbon atom more than amide
7176.

Nitroso amines \[({{R}_{2}}N-N=O)\] are soluble in water. On heating them with concentrated \[{{H}_{2}}S{{O}_{4}}\] they give secondary amines. The reaction is called               [AFMC 1998; AIIMS 1998; BHU 2002]

A.                 Perkin's reaction
B.                 Fittig's reaction
C.                 Sandmeyer's reaction
D.                 Liebermann's nitroso reaction
Answer» E.
7177.

The strongest base among the following is [AIIMS 2004; BHU 2004]

A.                                  
B.                
C.                  
D.                
Answer» D.                
7178.

If N and S are present in an organic compound during Lassaigne test, then both changes into      [CPMT 1997]

A.                 \[N{{a}_{2}}S\] and \[NaCN\]
B.                 NaSCN
C.                 \[N{{a}_{2}}S{{O}_{3}}\] and NaCN
D.                 \[N{{a}_{2}}S\] and NaCNO
Answer» C.                 \[N{{a}_{2}}S{{O}_{3}}\] and NaCN
7179.

\[RN{{H}_{2}}\] reacts with \[{{C}_{6}}{{H}_{5}}S{{O}_{2}}Cl\] in aqueous \[KOH\] to give a clear solution. On acidification a precipitate is obtained which is due to the formation of [Roorkee 2000]

A.                 \[R-\underset{H\,\,\,}{\overset{H\,\,}{\mathop{\underset{|\,\,\,\,}{\overset{|\,\,\,\,}{\mathop{{{N}^{+}}}}}\,}}}\,-S{{O}_{2}}{{C}_{6}}{{H}_{5}}O{{H}^{-}}\]
B.                 \[R-{{N}^{-}}S{{O}_{2}}{{C}_{6}}{{H}_{5}}{{K}^{+}}\]
C.                 \[R-NHS{{O}_{2}}{{C}_{6}}{{H}_{5}}\]
D.                 \[{{C}_{6}}{{H}_{5}}S{{O}_{2}}N{{H}_{2}}\]
Answer» D.                 \[{{C}_{6}}{{H}_{5}}S{{O}_{2}}N{{H}_{2}}\]
7180.

The following reaction is               [KCET 1996]

A.                 Nucleophilic substitution
B.                 Electrophilic substitution
C.                 Free radical substitution
D.                 None of these
Answer» B.                 Electrophilic substitution
7181.

Order of basicity of ethyl amines is          [MP PMT/PET 1988]

A.                 Secondary > Primary > Tertiary
B.                 Primary > Secondary > Tertiary
C.                 Secondary > Tertiary > Primary
D.                 Tertiary > Primary > Secondary
Answer» B.                 Primary > Secondary > Tertiary
7182.

The refluxing of \[{{(C{{H}_{3}})}_{2}}NCOC{{H}_{3}}\] with acid gives [KCET 1996]

A.                 \[2C{{H}_{3}}N{{H}_{2}}+C{{H}_{3}}COOH\]
B.                 \[2C{{H}_{3}}OH+C{{H}_{3}}COOH\]
C.                 \[{{(C{{H}_{3}})}_{2}}NH+C{{H}_{3}}COOH\]
D.                 \[{{(C{{H}_{3}})}_{2}}NCOOH+C{{H}_{4}}\]
Answer» D.                 \[{{(C{{H}_{3}})}_{2}}NCOOH+C{{H}_{4}}\]
7183.

The order of basic strength among the following amines in benzene solution is  [AIIMS 1991; RPMT 2002]

A.                 \[C{{H}_{3}}N{{H}_{2}}>{{(C{{H}_{3}})}_{3}}N>{{(C{{H}_{3}})}_{2}}NH\]
B.                 \[{{(C{{H}_{3}})}_{2}}NH>C{{H}_{3}}N{{H}_{2}}>{{(C{{H}_{3}})}_{3}}N\]
C.                 \[C{{H}_{3}}N{{H}_{2}}>{{(C{{H}_{3}})}_{2}}NH>{{(C{{H}_{3}})}_{3}}N\]
D.                 \[{{(C{{H}_{3}})}_{3}}N>C{{H}_{3}}N{{H}_{2}}>{{(C{{H}_{3}})}_{2}}NH\]
Answer» C.                 \[C{{H}_{3}}N{{H}_{2}}>{{(C{{H}_{3}})}_{2}}NH>{{(C{{H}_{3}})}_{3}}N\]
7184.

 \[+\,CHC{{l}_{3}}+KOH\to ?\]                 [BHU 2000; Pb. PMT 2000; Kerala 2003]

A.                 Phenyl isocyanide           
B.                 Benzyl amine
C.                 Benzyl chloride
D.                 None of these
Answer» B.                 Benzyl amine
7185.

The compound      Forms nitro so amines when the substituents are  [Roorkee 1999]

A.                 \[{{R}_{1}}=C{{H}_{3}},\,{{R}_{2}}={{R}_{3}}=H\]
B.                 \[{{R}_{1}}={{R}_{2}}=H,\,\,{{R}_{3}}={{C}_{2}}{{H}_{5}}\]
C.                 \[{{R}_{1}}=H,\,\,{{R}_{2}}={{R}_{3}}=C{{H}_{3}}\]
D.                 \[{{R}_{1}}=C{{H}_{3}},\,\,{{R}_{2}}={{C}_{2}}{{H}_{5}},\,\,{{R}_{3}}=H\]
Answer» D.                 \[{{R}_{1}}=C{{H}_{3}},\,\,{{R}_{2}}={{C}_{2}}{{H}_{5}},\,\,{{R}_{3}}=H\]
7186.

  In the above reaction 'X' stands for [CPMT 1986, 2001; MP PET 1992; KCET (Engg./Med.) 2000]

A.                 \[N{{H}_{2}}\]  
B.                 \[SnC{{l}_{2}}\]
C.                 Cl           
D.                 \[NH_{4}^{+}C{{l}^{-}}\]
Answer» B.                 \[SnC{{l}_{2}}\]
7187.

Which conformation of \[{{C}_{6}}{{H}_{6}}C{{l}_{6}}\] is most powerful insecticide

A. aaeeee
B. aaaeee
C. aaaaee
D. aaaaaa
Answer» C. aaaaee
7188.

In which alkyl halide, \[S{{N}^{2}}\] mechanism is favoured maximum [RPMT 1997]

A. \[C{{H}_{3}}Cl\]
B. \[C{{H}_{3}}C{{H}_{2}}Cl\]
C. \[{{(C{{H}_{3}})}_{2}}CHCl\]
D. \[{{(C{{H}_{3}})}_{3}}C-Cl\]
Answer» B. \[C{{H}_{3}}C{{H}_{2}}Cl\]
7189.

The hybridization state of carbon atoms in the product formed by the reaction of ethyl chloride with aqueous potassium hydroxide is [EAMCET 1997]

A. sp
B. \[s{{p}^{2}}\]
C. \[s{{p}^{3}}\]
D. \[s{{p}^{3}}d\]
Answer» D. \[s{{p}^{3}}d\]
7190.

When but -3-en -2- ol reacts with aq. HBr, the product formed is [DCE 2001]

A. 3 - bromobut - 1- ene
B. 1 - bromobut - 2- ene 
C. A mixture of both a and b
D. 2 - bromobut - 2 - ene
Answer» D. 2 - bromobut - 2 - ene
7191.

In which one of the following conversions phosphorus pentachloride is used as a reagent [EAMCET 1997]

A. \[{{H}_{2}}C=C{{H}_{2}}\to C{{H}_{3}}C{{H}_{2}}Cl\]
B. \[{{H}_{3}}C-O-C{{H}_{3}}\to C{{H}_{3}}Cl\]
C. \[C{{H}_{3}}C{{H}_{2}}OH\to C{{H}_{3}}C{{H}_{2}}Cl\]
D. \[HC\equiv CH\to C{{H}_{2}}=CHCl\]
Answer» C. \[C{{H}_{3}}C{{H}_{2}}OH\to C{{H}_{3}}C{{H}_{2}}Cl\]
7192.

Which of the following is the example of \[S{{N}^{2}}\] reaction [CPMT 1999]

A. \[C{{H}_{3}}Br+O{{H}^{-}}-C{{H}_{3}}OH+B{{r}^{-}}\]
B. \[\underset{\underset{\,Br\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,OH\,\,\,}{\mathop{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,\,}}\,}{\mathop{C{{H}_{3}}CHC{{H}_{3}}+O{{H}^{-}}\xrightarrow{{}}C{{H}_{3}}CHC{{H}_{3}}+B{{r}^{-}}}}\,\]
C. \[C{{H}_{3}}C{{H}_{2}}OH\xrightarrow{-{{H}_{2}}O}C{{H}_{2}}=C{{H}_{2}}\]
D. \[\underset{\underset{\,Br\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,H\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}}\,}{\mathop{\overset{\overset{C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,C{{H}_{3}}\,\,\,\,\,\,\,\,\,\,\,\,\,\,}{\mathop{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,}}\,}{\mathop{C{{H}_{3}}-C-C{{H}_{3}}+O{{H}^{-}}\to C{{H}_{3}}-C-O-C{{H}_{3}}+B{{r}^{-}}}}\,}}\,\]
Answer» B. \[\underset{\underset{\,Br\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,OH\,\,\,}{\mathop{|\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,\,|\,\,\,\,\,\,\,\,\,\,}}\,}{\mathop{C{{H}_{3}}CHC{{H}_{3}}+O{{H}^{-}}\xrightarrow{{}}C{{H}_{3}}CHC{{H}_{3}}+B{{r}^{-}}}}\,\]
7193.

An isomer of \[{{C}_{3}}{{H}_{6}}C{{l}_{2}}\]on boiling with aqueous KOH gives acetone. Hence, the isomer is [UPSEAT 2000]

A. 2, 2-dichloropropane
B. 1, 2-dichloropropane
C. 1, 1-dichloropropane
D. 1, 3-dichloropropane
Answer» B. 1, 2-dichloropropane
7194.

A new carbon-carbon bond formation is possible in [IIT-JEE 1998]

A. Cannizzaro reaction
B. Friedel-Craft's alkylation
C. Clemmensen reduction
D. Reimer-Tiemann reaction
Answer» C. Clemmensen reduction
7195.

The odd decomposition of carbon chlorine bond form [UPSEAT 1999]

A. Two free ions
B. Two-carbanium ion
C. Two carbanion
D. A cation and an anion
Answer» E.
7196.

When CHCl3 is boiled with NaOH, It gives    [Orissa JEE 2003]

A. Formic acid
B. Trihydroxy methane
C. Acetylene
D. Sodium formate
Answer» C. Acetylene
7197.

Among the following, the molecule with the highest dipole moment is           [IIT-JEE (Screening) 2003]

A. \[C{{H}_{3}}Cl\]
B. \[C{{H}_{2}}C{{l}_{2}}\]
C. \[CHC{{l}_{3}}\]
D. \[CC{{l}_{4}}\]
Answer» B. \[C{{H}_{2}}C{{l}_{2}}\]
7198.

The oxidation potential of a hydrogen electrode at pH = 10 and \[p{{H}_{1}}=1\]                                               [JIPMER 2000]

A.                 0.059 V
B.                 0.59 V
C.                 0.00 V   
D.                 0.51 V
Answer» C.                 0.00 V   
7199.

A gas \[X\] at \[1\,atm\] is bubbled through a solution containing a mixture of \[1\,M\,{{Y}^{-}}\] and \[1\,M\,{{Z}^{-}}\] at \[{{25}^{o}}C\]. If the reduction potential of \[Z>Y>X\], then         [IIT 1999]

A.                 \[Y\] will oxidize \[X\] and not \[Z\]                
B.                 \[Y\] will oxidize \[Z\] and not \[X\]
C.                 \[Y\] will oxidize both \[X\] and \[Z\]
D.                 \[Y\] will reduce both \[X\] and \[Z\]
Answer» B.                 \[Y\] will oxidize \[Z\] and not \[X\]
7200.

The standard \[EMF\] for the given cell reaction \[Zn+C{{u}^{2+}}=Cu+Z{{n}^{2+}}\] is \[1.10V\] at \[{{25}^{o}}C\]. The \[EMF\] for the cell reaction, when \[0.1M\,C{{u}^{2+}}\] and \[0.1M\,Z{{n}^{2+}}\] solutions are used, at \[{{25}^{o}}C\] is [MNR 1994; AMU 1999; UPSEAT 2002]

A.                 \[1.10\,V\]         
B.                 \[0.110\,V\]
C.                 \[-1.10\,V\]       
D.                 \[-\,0.110\,V\]
Answer» B.                 \[0.110\,V\]