Q1. The product of \( \ce{CH3CONH2} \) undergoing Hoffmann bromamide reaction is:A. \( \ce{CH3CH2NH2} \)B. \( \ce{CH3NH2} \)C. \( \ce{(CH3)2NH} \)D. \( \ce{CH3OH} \)
Q2. An alkyl halide \( X \) with \( \ce{NH3} \) gives \( \ce{CH3CH2CH2CH2NH2} \). \( X \) is:A. \( \ce{CH3CH2Cl} \)B. \( \ce{CH3CH2CH2Cl} \)C. \( \ce{CH3Cl} \)D. \( \ce{CH3CH2CH2CH2Cl} \)
Q3. Which of the following is not a method to prepare primary amines as per the PDF?A. Reduction of nitro compoundsB. Hoffmann bromamide reactionC. Gabriel phthalimide synthesisD. Friedel-Crafts alkylation
Q4. A compound \( X \) on reduction with \( \ce{H2/Ni} \) gives \( \ce{CH3CH2CH2NH2} \). \( X \) is:A. \( \ce{CH3CH2CH2NO2} \)B. \( \ce{CH3CH2CH2OH} \)C. \( \ce{CH3CH2CHO} \)D. \( \ce{CH3CH2CH2Cl} \)
Q5. Which amine does not react with \( \ce{HNO2} \) to form an alcohol?A. \( \ce{CH3NH2} \)B. \( \ce{CH3CH2NH2} \)C. \( \ce{(CH3)3N} \)D. \( \ce{CH3CH2CH2NH2} \)
Q6. Why does aniline not undergo Friedel-Crafts reaction?A. Due to steric hindranceB. Due to low reactivityC. Due to resonanceD. Due to salt formation with \( \ce{AlCl3} \)
Q8. Which amine does not react with benzenesulphonyl chloride?A. \( \ce{CH3CH2NH2} \)B. \( \ce{(CH3CH2)2NH} \)C. \( \ce{(CH3CH2CH2)3N} \)D. \( \ce{C6H5NH2} \)
Q9. Which method is used to prepare \( \ce{CH3CH2CH2NH2} \) from \( \ce{CH3CH2CH2Cl} \)?A. Hoffmann bromamide reactionB. Reduction of nitro compoundsC. Gabriel phthalimide synthesisD. Ammonolysis
Q10. The product of aniline with \( \ce{H2SO4} \) at 453-473 K is:A. o-Aminobenzene sulphonic acidB. m-Aminobenzene sulphonic acidC. Anilinium sulphateD. p-Aminobenzene sulphonic acid