A) -NO B) -NH2 C) -ONO2 D) -NO2
A) Non-polar B) Weakly electron-withdrawing C) Strongly electron-donating D) Strongly electron-withdrawing
A) Reducing agent B) Explosophore C) Catalyst D) Oxidizer
A) It retards the reaction B) It facilitates the reaction C) It has no effect D) It terminates the reaction
A) Nitrosonium ion B) Nitrite ion C) Nitrate ion D) Nitronium ion
A) Trinitrotoluene B) Nitrobenzene C) Nitromethane D) Picric acid
A) Nitromethane B) Chloramphenicol C) Picric acid D) Nitrobenzene
A) Ammonium nitrite B) Sodium nitrate C) Silver nitrite D) Potassium nitrate
A) A defensive toxin B) A digestive enzyme C) An aggregation pheromone D) A reproductive hormone
A) 100–200 °C B) 350–450 °C C) 20–50 °C D) 600–700 °C
A) ter Meer reaction B) Krapcho decarboxylation variant C) Zinke nitration D) Meyer synthesis
A) Neutral B) Amphoteric C) Basic D) Acidic
A) Edmund ter Meer B) Hans Krapcho C) Viktor Meyer D) Gustav Zinke
A) Nitropentadecene B) Chloramphenicol C) Aristolochic acid D) 3-Nitropropionic acid
A) Nitration by atmospheric nitrogen B) Oxidation of amino groups C) Dehydration of nitrites D) Reduction of nitrates
A) Hydrochloric acid B) Phosphoric acid C) Sulfuric acid D) Acetic acid
A) Preparation of nitroarenes from phenols B) Production of aliphatic nitro dimers C) Oxidation of amines D) Synthesis of nitroalkanes
A) It produces a 1,2-dinitro dimer B) It produces a nitroalkene C) It remains unchanged D) It produces nitromethane
A) Carboxyl group B) Hydroxyl group C) Nitro group D) Amino group
A) Termites B) Fungi and plants C) Bacteria only D) Ticks |