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Treatment of primary amines with nitrous acid gives diazonium ions, which decompose under the diazotization conditions to give a complex mixture of products. Aryldiazonium ions are stable and is a valuable intermediate. They react with activated aromatic compounds to give a coupling product. Which of the following diazonium ion is the most reactive towards an azo coupling reaction? |
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Answer» Treatment of primary amines with nitrous acid gives diazonium ions, which decompose under the diazotization conditions to give a complex mixture of products. Aryldiazonium ions are stable and is a valuable intermediate. They react with activated aromatic compounds to give a coupling product. |
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