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This section includes InterviewSolutions, each offering curated multiple-choice questions to sharpen your knowledge and support exam preparation. Choose a topic below to get started.
| 51. |
On treatment with chlorine in presence of sunlight toluene gives the product .A. o-chloro toueneB. 2,5-dichloro tolueneC. p-chloro touleneD. Benzyl chloride |
| Answer» Correct Answer - D | |
| 52. |
A solution of (-l)- chloro -1 phenyletane in toluene recemises slowly in the presence of a small amunt of `SbCI_(5)` due to the formation of .A. carbonionB. carbeneC. carbocationsD. free radical |
| Answer» Correct Answer - C | |
| 53. |
Bromination of cyclohexene under conditions gives below yields: A. B. C. D. |
| Answer» Correct Answer - D | |
| 54. |
Toluene, when treated with `Br_(2)Fe`, gives o and p-bromotoluene, because the `CH_(3)` group-A. is ortho and para directingB. is meta directingC. deactivates the ring by hyperconjugationD. deactivates the ring |
| Answer» Correct Answer - A | |
| 55. |
Chlorination of toluene in the presence of light and heat followed by treatment with aqueous NaOH givesA. o-cresolB. p-cresolC. 2,4 dihydroxytolueneD. Benzoic acid |
| Answer» Correct Answer - D | |
| 56. |
Bencyl chloride `(C_(6)H_(5)CH_(2)CI)` can be prepared from toluene by chlorination withA. `SO_(2)CI_(2)`B. `SOCI_(2)`C. `PCI_(5)`D. `NaOCI_(2)` |
| Answer» Correct Answer - A | |
| 57. |
Statement-I: Free radical chlorination of n-butane gives `72%` of 2-chlorobutane and `28%` of 1-chlorobutane though it has six primary and four secondary hydrogens. Because Statement-II: A secondary hydrogen is abstracted more easily than the primary hydrogen.A. Statement-I is True, Statement-II is True, Statement-II is a correct explanation for Statement-IB. Statement-I is True, Statement-II is True, Statement-II is NOT a correct explanation for Statement-IC. Statement-I is True, Statement-II is False.D. Statement-I is False, Statement-II is True. |
| Answer» Correct Answer - A | |
| 58. |
Statement-I: Optically active 2-idoibutane on treatment with `NaI` in acetone undergoes racemisation. Because Statement-II: Repeated Walden inversions on the reactant and its product evantually gives a racemic mixure.A. Statement-I is True, Statement-II is True, Statement-II is a correct explanation for Statement-IB. Statement-I is True, Statement-II is True, Statement-II is NOT a correct explanation for Statement-IC. Statement-I is True, Statement-II is False.D. Statement-I is False, Statement-II is True. |
| Answer» Correct Answer - A | |
| 59. |
Grignard reagent is obtained when magnesium is treated withA. Alkyl halide in presence of alcoholB. Alkyl halide in presence of phenolC. Alkyl halide in presence of dry etherD. Alkyl halide in presence of alcoholated ether |
| Answer» Correct Answer - C | |
| 60. |
The reagent(s) for the following conversion is/are:A. alcoholic `KOH`B. Alcoholic `KOH` followed by `NaNH_(2)`C. aqueous `KOH` followed by `NaNH_(2)`D. `Zn//CH_(3)OH` |
| Answer» Correct Answer - B | |
| 61. |
Grignard reagent can be prepared byA. `CH_(3)-CH_(2)-CI +Mg overset("dry")underset("ether")rarr`B. `CH_(3)-underset(CI)underset(|)(CH)-underset(OH)underset(|)(CH_(2)) +Mg overset("dry")underset("ether")rarr`C. `CH_(3)-overset(CH_(3))overset(|)underset(CH_(3))underset(|)(C)-OH +Mg overset("dry")underset("ether")rarr`D. All of them |
| Answer» Correct Answer - A | |
| 62. |
For the reaction A. `CH_(3)-CH=CH-CH_(3)` predominatesB. `CH_(2)=CH-CH_(2)-CH_(3)` predominatesC. Both are formed in equal amountsD. The product ratio depends on the halogen |
| Answer» Correct Answer - D | |
| 63. |
Most stable carbocation formed from `(CH_(3))_(3)C-Br,(C_(6)H_(5))_(3)CBr,(C_(6)H_(5))_(2)CHBr` and `C_(6)H_(5)CH_(2)Br` would beA. `C_(6)H_(5)overset(o+)(CH_(2))`B. `(CH_(3))_(3)overset(o+)(C)`C. `(C_(6)H_(5))_(3)overset(o+)(C)`D. `(C_(6)H_(5))_(2)overset(o+)(CH)` |
| Answer» Correct Answer - C | |