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