Q1. The amide that produces propanamine via Hoffmann bromamide reaction is:A. \( \ce{CH3CONH2} \)B. \( \ce{CH3CH2CH2CONH2} \)C. \( \ce{CH3CH2CONH2} \)D. \( \ce{C6H5CONH2} \)
Q2. The product of \( \ce{C6H5NO2} \) reduction with \( \ce{Sn/HCl} \) is:A. \( \ce{C6H5OH} \)B. \( \ce{C6H6} \)C. \( \ce{C6H5CH3} \)D. \( \ce{C6H5NH2} \)
Q3. Which method reduces \( \ce{RCONH2} \) to \( \ce{RNH2} \) with one less carbon?A. Gabriel phthalimide synthesisB. Reduction of nitro compoundsC. AmmonolysisD. Hoffmann bromamide reaction
Q4. Which of the following amines can form hydrogen bonds with water?A. \( \ce{CH3CH2NH2} \)B. \( \ce{(CH3)3N} \)C. \( \ce{(CH3CH2)3N} \)D. \( \ce{CH3CH2CH2N(CH3)2} \)
Q5. Which reagent converts aniline to acetanilide?A. \( \ce{CH3Cl} \)B. \( \ce{CH3COCl} \)C. \( \ce{CH3OH} \)D. \( \ce{HNO2} \)
Q6. The product of \( \ce{CH3CH2NH2} \) reacting with \( \ce{HNO2} \) at 273-278 K is:A. \( \ce{CH3CH2NO} \)B. \( \ce{CH3CH2Cl} \)C. \( \ce{CH3CHO} \)D. \( \ce{CH3CH2OH} \)
Q7. The product of \( \ce{CH3NH2} \) with \( \ce{CHCl3} \) and alcoholic KOH is:A. \( \ce{CH3OH} \)B. \( \ce{CH3NC} \)C. \( \ce{CH3Cl} \)D. \( \ce{CH3NHCH3} \)
Q8. Which amine reacts with \( \ce{CHCl3} \) and alcoholic KOH to produce a compound with a characteristic odor?A. \( \ce{CH3CH2NH2} \)B. \( \ce{(CH3CH2)2NH} \)C. \( \ce{(CH3)3N} \)D. \( \ce{CH3CH2N(CH3)2} \)
Q9. Which amine shows the least solubility in water?A. \( \ce{CH3NH2} \)B. \( \ce{CH3CH2NH2} \)C. \( \ce{(CH3CH2CH2)3N} \)D. \( \ce{(CH3CH2)2NH} \)
Q10. Which amine produces a yellow oily compound when treated with \( \ce{HNO2} \)?A. \( \ce{CH3NH2} \)B. \( \ce{(CH3)2NH} \)C. \( \ce{(CH3)3N} \)D. \( \ce{C6H5NH2} \)