When treating a primary aliphatic amine () with nitrous acid () generated in situ at ice-cold temper — Alcohols Phenols and Ethers Chemistry Question
Question
When treating a primary aliphatic amine ($R-CH_2-NH_2$) with nitrous acid ($HNO_2$) generated in situ at ice-cold temperatures, what is the major organic product ultimately isolated?
Answer: A
💡 Solution & Explanation
Aliphatic primary amines react with nitrous acid ($HNO_2$) to yield highly unstable aliphatic diazonium salts. These immediately decompose even at low temperatures to form primary alcohols ($R-CH_2-OH$) along with the vigorous evolution of nitrogen gas.
💬Ask on WhatsApp →
Still have doubts about this question?
Send it to our AI chemistry tutor on WhatsApp — gets answered in minutes