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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. \[0.110\,V\] | |