How to Predict where an Electrophilic Aromatic Substitution May Occur in a Ring – Part 4
An organic reaction in which an atom attached to an aromatic system (usually hydrogen) is substituted by an electrophile is referred to as electrophilic aromatic substitution (SEAr or EAS).
One of the most important EASs is diazotization (aka diazonium salt formation reaction, or diazoniation, or diazotation, or Griess diazo reaction), which is synthetically versatile as the salt can react with a variety of nucleophiles. These reactions take place by the aromatic nucleophilic substitution unimolecular mechanism (NAS, SN1Ar or SRN1).
During diazotization of primary arylamines, an excess of mineral acid is 'typically' used as the acid prevents the coupling of the diazonium salt formed with the arylamine by converting the arylamine to its salt (deactivation of the p-position of the arylamine).
An azo coupling is a reaction between an aromatic diazonium compound and an activated aromatic compound that produces an azo derivative.
Question:
Predict the major product(s) of the following reaction:
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Solution infographic:
OPD = o-Phenylenediamine
For a wheel of diazotization reactions, click here.
Coupled with coupling reactions❓ Let Chemaficionado know in the comments below or at mychemistryhomework@gmail.com❗
References:
(1) Wikipedia Contributors. Electrophilic aromatic substitution. Wikipedia. https://en.wikipedia.org/wiki/Electrophilic_aromatic_substitution.
(2) Diazonium compound. Wikipedia. https://en.wikipedia.org/wiki/Diazonium_compound.
(3) Azo coupling. Wikipedia. https://en.wikipedia.org/wiki/Azo_coupling.
(4) Chouhan, M. S. Advanced Problems in Organic Chemistry for JEE, 11th Ed.
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