Which of the following would not be a good choice for reducing nitrobenzene to aniline

  1. Solved 5. One synthetic preparation of aniline involves
  2. Solved Which of the following conditions will allow for the
  3. Solved Q17 Aniline was synthesized by reducing nitrobenzene
  4. Sciencemadness Discussion Board


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Solved 5. One synthetic preparation of aniline involves

This problem has been solved! You'll get a detailed solution from a subject matter expert that helps you learn core concepts. See Answer See Answer See Answer done loading Question:5. One synthetic preparation of aniline involves reducing nitrobenzene with iron and HCl, and then steam distilling the resultant aniline at 99 °C. How much aniline codistills with each gram of water during the steam distillation?

Solved Which of the following conditions will allow for the

This problem has been solved! You'll get a detailed solution from a subject matter expert that helps you learn core concepts. See Answer See Answer See Answer done loading Question:Which of the following conditions will allow for the reduction of a nitrobenzene to aniline? (Select all that are possible) HCl, Fe Br2, FeBr3 H2, Pt H2

Solved Q17 Aniline was synthesized by reducing nitrobenzene

This problem has been solved! You'll get a detailed solution from a subject matter expert that helps you learn core concepts. See Answer See Answer See Answer done loading Question:Q17 Aniline was synthesized by reducing nitrobenzene with the aid of appropriate reagents. Suppose 82 % of the initial amount of nitrobenzene reacted and 18.6 g of aniline was obtained. How many grams of nitrobenzene were initially used? From the following 1-6 choose the closest value. 17 g 20 25 3 30 4 35 40 6 45 Q17 Aniline was synthesized by reducing nitrobenzene with the aid of appropriate reagents. Suppose 82 % of the initial amount of nitrobenzene reacted and 18.6 g of aniline was obtained. How many grams of nitrobenzene were initially used? From the following 1-6 choose the closest value. 17 g 20 25 3 30 4 35 40 6 45 Previous question Next question

Sciencemadness Discussion Board

Posts: 103 Registered: 19-7-2019 Member Is Offline Reduction of nitrobenzene by zinc and ammonium chloride Hi, I've been studying the following reaction: PhNO3 + Zn + NH4Cl --> Ph-NH-OH + ZnO + ? I can't find much information on this. In particular, I'm looking for a reaction mechanism. I can't seem to find any anywhere. What role does the ammonium chloride play in this reaction? Why ammonium chloride in particular, and why zinc in particular? Thanks, Thor Posts: 48 Registered: 9-10-2017 Member Is Offline Mood: No Mood Vogel's Textbook of Practical Organic Chemistry: Quote: The reduction of an aromatic nitro compound with a powerful reducing agent (tin or tin(II) chloride and hydrochloric acid; iron and dilute hydrochloric acid; hydrogen and a platinum catalyst) leads to a good yield of primary amine, e.g. aniline from nitrobenzene. By the use of milder reducing agents and by the control of the hydrogen ion concentration of the solution, a number of intermediate products may be isolated, some of which are products of direct reduction and others are formed through secondary reactions. Zn and NH 4Cl can be replaced by other reducing agents/solvents. Mechanism (I'm looking for a reputable source): [Edited on 31-7-2019 by icelake] [Edited on 31-7-2019 by icelake] Posts: 103 Registered: 19-7-2019 Member Is Offline Quote: Vogel's Textbook of Practical Organic Chemistry: Quote: The reduction of an aromatic nitro compound with a powerful reducing agent (tin or tin(II) chloride and...

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