 
			 
			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 reaction sequence that will best carry out the following preparation? | 
| A. | i I + MeONa + CH3H2Br ii) neutralize | 
| B. | i) I + EtONa ii) CH3CH2Br iii) neutralize | 
| C. | i) CH3CH2Br + Mg, Et2O ii) Add I iii) neutralize | 
| D. | i) I + CH3CH2OH + Mg ii) neutralize | 
| Answer» D. i) I + CH3CH2OH + Mg ii) neutralize | |
| 2. | Which of the following compounds would not give tert-butyl alcohol when treated with excess methylmagnesium bromide? | 
| A. | acetyl chloride | 
| B. | acetaldehyde | 
| C. | methyl acetate | 
| D. | acetic anhydride | 
| Answer» C. methyl acetate | |
| 3. | Which of the following compounds gives a primary alcohol upon reaction with phenylmagnesium bromide? | 
| A. | 2-methyloxirane | 
| B. | ethylene oxide | 
| C. | ethyl formate | 
| D. | carbon dioxide | 
| Answer» C. ethyl formate | |
| 4. | A Grignard’s reagent may be made by reacting magnesium with which of the following compound? | 
| A. | Methyl amine | 
| B. | Diethyl ether | 
| C. | Ethyl iodide | 
| D. | Ethyl alcohol | 
| Answer» D. Ethyl alcohol | |
| 5. | Which of the following compounds gives a secondary alcohol upon reaction with methylmagnesium bromide? | 
| A. | Butyl formate | 
| B. | 3- pentanone | 
| C. | Pentanal | 
| D. | Methyl butanoate | 
| Answer» D. Methyl butanoate | |
| 6. | Alkyl halides can be converted into Grignard reagents by _______________ | 
| A. | Boiling them with Mg ribbon in alcoholic solution | 
| B. | Warming them with magnesium powder in dry ether | 
| C. | Refluxing them with MgCl2 solution | 
| D. | Warming them with Mgcl2 | 
| Answer» C. Refluxing them with MgCl2 solution | |
| 7. | WHICH_OF_THE_FOLLOWING_COMPOUNDS_WOULD_NOT_GIVE_TERT-BUTYL_ALCOHOL_WHEN_TREATED_WITH_EXCESS_METHYLMAGNESIUM_BROMIDE??$ | 
| A. | acetyl chloride | 
| B. | acetaldehyde | 
| C. | methyl acetate | 
| D. | acetic anhydride | 
| Answer» C. methyl acetate | |
| 8. | Which of the following reagents, when treated with phenylmagnesiuim bromide followed by acid workup, will yield 2-phenylethanol? | 
| A. | Ethanol | 
| B. | Diethyl ether | 
| C. | Ethanal | 
| D. | Oxirane | 
| Answer» E. | |
| 9. | Which of the following compounds gives a primary alcohol upon reaction with phenylmagnesium bromide? | 
| A. | 2-methyloxirane | 
| B. | ethylene oxide | 
| C. | ethyl formate | 
| D. | carbon dioxide | 
| Answer» C. ethyl formate | |
| 10. | A Grignard’s reagent may be made by reacting magnesium with which of the following compound?$ | 
| A. | Methyl amine | 
| B. | Diethyl ether | 
| C. | Ethyl iodide | 
| D. | Ethyl alcohol | 
| Answer» D. Ethyl alcohol | |
| 11. | Which of the following statements about Grignard reagent is false? | 
| A. | Grignard reagents (RMgBr) add to the carbonyl group of aldehydes and ketones | 
| B. | An organosodium compound is not very reactive compared to a Grignard reagent | 
| C. | Grignard reagents are prepared in ether or tetrahydrofuran (THF) | 
| D. | Grignard reagents are decomposed by water and alcohol | 
| Answer» C. Grignard reagents are prepared in ether or tetrahydrofuran (THF) | |
| 12. | Which of the following compounds does not give a tertiary alcohol upon reaction with methylmagnesium bromide? | 
| A. | 3-methylpentanal | 
| B. | Ethyl benzoate | 
| C. | 4,4-dimethylcyclohexanone | 
| D. | 4-heptanone | 
| Answer» E. | |
| 13. | Which is not present in Grignard reagent? | 
| A. | Methyl group | 
| B. | Magnesium | 
| C. | Halogen | 
| D. | ‚àíCOOH group | 
| Answer» E. | |
| 14. | Alkyl halides can be converted into Grignard reagents by | 
| A. | Boiling them with Mg ribbon in alcoholic solution | 
| B. | Warming them with magnesium powder in dry ether | 
| C. | Refluxing them with MgCl<sub>2</sub> solution | 
| D. | Warming them with Mgcl<sub>2</sub> | 
| Answer» C. Refluxing them with MgCl<sub>2</sub> solution | |