 
			 
			MCQOPTIONS
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				This section includes 14 Mcqs, each offering curated multiple-choice questions to sharpen your Organic Chemistry knowledge and support exam preparation. Choose a topic below to get started.
| 1. | Which of the following cannot react as a nucleophile? | 
| A. | CH3NH2 | 
| B. | (CH3)2NH | 
| C. | (CH3)3N | 
| D. | (CH3)4N+ | 
| Answer» E. | |
| 2. | Which halide ion is the best nucleophile in dimethyl sulfoxide solution? | 
| A. | I– | 
| B. | F– | 
| C. | Cl– | 
| D. | Br– | 
| Answer» C. Cl– | |
| 3. | Which of the following statements is true about the following two anionic molecules? | 
| A. | I is more basic and more nucleophilic than II | 
| B. | I is less basic and less nucleophilic than II | 
| C. | I is more basic but less nucleophilic than II | 
| D. | I is less basic but more nucleophilic than II | 
| Answer» D. I is less basic but more nucleophilic than II | |
| 4. | What will be the number of products (excluding stereoisomers) in the given reaction? C6H5CHO + CH3-CHO + NaOH → Product | 
| A. | One | 
| B. | Three | 
| C. | Two | 
| D. | Four | 
| Answer» D. Four | |
| 5. | Which of the following nucleophile can be used for partial enolization 1,3-Dicarbonyl compound?a) Lithium di-isopropyl amide (LD | 
| A. | Lithium di-isopropyl amide (LDA) | 
| B. | Et-O– | 
| C. | Weak base like NaOH | 
| D. | Sodium acetate | 
| Answer» E. | |
| 6. | Which of the following is not true about nucleophile? | 
| A. | donates an electron pair to an electrophile to form a chemical bond | 
| B. | all molecules or ions with a free pair of electrons or at least one pi bond can act as nucleophiles | 
| C. | nucleophile are Lewis acids by definition | 
| D. | a nucleophile becomes attracted to a full or partial positive charge | 
| Answer» D. a nucleophile becomes attracted to a full or partial positive charge | |
| 7. | WHICH_HALIDE_ION_IS_THE_BEST_NUCLEOPHILE_IN_DIMETHYL_SULFOXIDE_SOLUTION??$ | 
| A. | I<sup>–</sup> | 
| B. | F<sup>–</sup> | 
| C. | Cl<sup>–</sup> | 
| D. | Br<sup>–</sup> | 
| Answer» C. Cl<sup>‚Äö√Ñ√∂‚àö√ë‚àö¬®</sup> | |
| 8. | Which of the following cannot react as a nucleophile?$ | 
| A. | CH<sub>3</sub>NH<sub>2</sub> | 
| B. | (CH<sub>3</sub>)<sub>2</sub>NH | 
| C. | (CH<sub>3</sub>)<sub>3</sub>N | 
| D. | (CH<sub>3</sub>)<sub>4</sub>N<sup>+</sup> | 
| Answer» E. | |
| 9. | Which of the following statements is true about ammonia and water? | 
| A. | ammonia is more basic and more nucleophilic than water | 
| B. | ammonia is less basic and less nucleophilic than water | 
| C. | ammonia is more basic but less nucleophilic than water | 
| D. | ammonia is less basic but more nucleophilic than water | 
| Answer» B. ammonia is less basic and less nucleophilic than water | |
| 10. | Which reagent is a good nucleophile? | 
| A. | NH<sub>3</sub> | 
| B. | BH<sub>3</sub> | 
| C. | Br<sub>2</sub> | 
| D. | HBr | 
| Answer» B. BH<sub>3</sub> | |
| 11. | What will be the number of products (excluding stereoisomers) in the given reaction? | 
| A. | |
| B. | One | 
| C. | Three | 
| Answer» D. | |
| 12. | Which of the following nucleophile can be used for partial enolization 1,3-Dicarbonyl compound? | 
| A. | Lithium di-isopropyl amide (LDA) | 
| B. | Et-O<sup>–</sup> | 
| C. | Weak base like NaOH | 
| D. | Sodium acetate | 
| Answer» E. | |
| 13. | Which halogen nucleophile is weakest in polar, aprotic solvents? | 
| A. | I<sup>–</sup> | 
| B. | F<sup>–</sup> | 
| C. | Cl<sup>–</sup> | 
| D. | Br<sup>–</sup> | 
| Answer» B. F<sup>‚Äö√Ñ√∂‚àö√ë‚àö¬®</sup> | |
| 14. | Which of the following is not true about nucleophile? | 
| A. | donates an electron pair to an electrophile to form a chemical bond | 
| B. | all molecules or ions with a free pair of electrons or at least one pi bond can act as nucleophiles | 
| C. | nucleophile are Lewis acids by definition | 
| D. | a nucleophile becomes attracted to a full or partial positive charge | 
| Answer» D. a nucleophile becomes attracted to a full or partial positive charge | |