Propose a plausible mechanism for the following transformation: For the mechanism, draw the curved arrows as needed. Include lon
e pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do not use abbreviations such as Me or Ph.
1 answer:
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Answer:
Secondary amines react with the nitrosonium ion to generate <span><u>N-Nitrosoamines</u>.
Explanation:
Nitosonium Ion is generally utilized in the formation of Diazonium Salts which are considered excellent starting Material from synthesis point of View. Diazonium salts are formed by reacting Primary Amine or Anilines with Nitrosonium Ions. In our case, the Amine given is Secondary. So, reaction of <em>Sec.</em> Amines with Nitrosonium Ions stops after the formation of N-Nitrosoamine as there is no Hydrogen attached to Nitrogen atom of Amine to be eliminated and form a double and eventually triple bond with the Nitrogen atom of Nitrosonium Ion.</span>
Secondary amines react with the nitrosonium ion to generate <span><u>N-Nitrosoamines</u>.
Explanation:
Nitosonium Ion is generally utilized in the formation of Diazonium Salts which are considered excellent starting Material from synthesis point of View. Diazonium salts are formed by reacting Primary Amine or Anilines with Nitrosonium Ions. In our case, the Amine given is Secondary. So, reaction of <em>Sec.</em> Amines with Nitrosonium Ions stops after the formation of N-Nitrosoamine as there is no Hydrogen attached to Nitrogen atom of Amine to be eliminated and form a double and eventually triple bond with the Nitrogen atom of Nitrosonium Ion.</span>