Imine formation is reversible. Imines can be hydrolyzed back to the corresponding primary amine under acidic aqueous conditions. Most aldehydes and ketones react with 2º-amines to give …

identify the product formed when a given amine reacts with a given acid chloride. identify the amine, the acid chloride, or both, needed to synthesize a given amide. write a reaction …

2018年9月24日 · The Cope rearrangement is an intramolecular, syn -selective elimination reaction that converts a tertiary amine to an alkene. Why might one use the Cope elimination …

Acyl chlorides and acid anhydrides react with primary and secondary amines without the presence of heat to form amides. Tertiary amines cannot be acylated due to the absence of a …

Reaction of Amines with Nitrous Acid. Nitrous acid (HNO 2 or HONO) reacts with aliphatic amines in a fashion that provides a useful test for distinguishing primary, secondary and tertiary …

In the Hinsberg test, an amine is reacted with benzene sulfonyl chloride. If a product forms, the amine is either a primary or secondary amine, because tertiary amines do not form stable …

Tertiary amines react with oxygen in the presence of platinum to give amides38 showing a strong preference for reaction at methyl groups. For example, oxidation of trimethylamine gives N,N …

Another electrophilic reagent, benzenesulfonyl chloride, reacts with amines in a fashion that provides a useful test for distinguishing primary, secondary and tertiary amines (the Hinsberg …

We’ve already studied the two most general reactions of amines—alkylation and acylation. As we saw earlier in this chapter, primary, secondary, and tert...

Acyl chlorides and acid anhydrides react with primary and secondary amines without the presence of heat to form amides. Tertiary amines cannot be acylated due to the absence of a …