How can you convert benzene to N-phenylethanamide in 3 steps?
Step 1: Nitration of benzene Benzene + conc. H2SO4 + conc. HNO3 with heat & under reflux --> Nitrobenzene Step 2: Reduction of nitrobenzene Nitrobenzene + tin + conc. HCl with heat & under reflux --> Phenylamine Step 3: Reacting phenylamine with an acid chloride Phenylamine + ethanoyl chloride --> N-phenylethanamide
KA
Related Chemistry A Level answers
All answers ▸Describe the stages of a heterogeneous catalyst reaction route.
In terms of Electrostatic Forces, Suggest why the ‘Electron Affinity’ of Fluorine has a Negative value.
What is the definition of Avogadro's constant and when should I use it?
Why can there be one major product and one minor product after electrophilic addition takes place across a double bond?