Aniline reacts with nitrous acid,HNO2,to yield a stable diazonium salt.This diazonium salt undergoes electrophilic aromatic substitution on activated aromatic rings to yield brightly colored azo compounds that are widely used as dyes.The intermediate structures for the mechanism of this reaction are given below.Show all electron flow with arrows for this mechanism on the structures provided. 
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Q1: Exhibit 16-2
Consider the Friedel-Crafts alkylation reaction below
Q2: Exhibit 16-1
MATCH a structure or term from
Q3: Exhibit 16-1
MATCH a structure or term from
Q4: Exhibit 16-1
MATCH a structure or term from
Q5: Exhibit 16-3
Consider the data below to answer
Q7: Exhibit 16-2
Consider the Friedel-Crafts alkylation reaction below
Q8: Exhibit 16-6
To answer the following question(s),refer to
Q9: Exhibit 16-1
MATCH a structure or term from
Q10: Would you expect (nitromethyl)benzene to be more
Q11: Exhibit 16-2
Consider the Friedel-Crafts alkylation reaction below
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