πŸ“Š Pharmaceutical Organic Chemistry 1
Q. The addition of HCN to carbonyl compounds is an example of ……….
  • (A) Nucleophilic substitution
  • (B) Electrophilic addition
  • (C) Nucleophilic addition
  • (D) Electrophilic substitution
πŸ’¬ Discuss
βœ… Correct Answer: (C) Nucleophilic addition
πŸ“Š Pharmaceutical Organic Chemistry 1
Q. The typical reactions of aldehyde is………………….
  • (A) Electrophilic addition
  • (B) Nucleophilic substitution
  • (C) Nucleophilic addition
  • (D) Nucleophilic elimination
πŸ’¬ Discuss
βœ… Correct Answer: (C) Nucleophilic addition
πŸ“Š Pharmaceutical Organic Chemistry 1
Q. Formaldehyde when treated with KOH gives methanol and potassium formate. The reaction is known as………..
  • (A) Perkin reaction
  • (B) Claisen reaction
  • (C) Cannizzaro reaction
  • (D) Knoevenagel reaction
πŸ’¬ Discuss
βœ… Correct Answer: (C) Cannizzaro reaction
πŸ“Š Pharmaceutical Organic Chemistry 1
Q. The compound obtained by the reduction of propionaldehyde by amalgamated zinc and concentrated HCl is…………….
  • (A) Propanol
  • (B) Propane
  • (C) Propene
  • (D) All of these
πŸ’¬ Discuss
βœ… Correct Answer: (B) Propane
πŸ“Š Pharmaceutical Organic Chemistry 1
Q. Which of the following does not turn Schiff's reagent to pink…………
  • (A) Formaldehyde
  • (B) Benzaldehyde
  • (C) Acetone
  • (D) Acetaldehyde
πŸ’¬ Discuss
βœ… Correct Answer: (C) Acetone