Glucose reacts with ammonia in the presence of a trace of acid to give predominantly -D- glucopyranosylamine.
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Glucose reacts with ammonia in the presence of a trace of acid to give predominantly β-D- glucopyranosylamine. Propose a reasonable mechanism for this transformation. Why is only the hydroxy group at C1 replaced?
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The detailed mechanism is given belowOnly C1 hydroxy...View the full answer
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Related Book For
Organic Chemistry structure and function
ISBN: 978-1429204941
6th edition
Authors: K. Peter C. Vollhardt, Neil E. Schore
Question Posted:
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