Glucose reacts with ammonia in the presence of a trace of acid to give predominantly D glucopyranosylamine Propose a reasonable mechanism for this transformation Why is only the hydroxy group at C1 replaced ...

The detailed mechanism is given belowOnly C1 hydroxy ...

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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Organic Chemistry structure and function

ISBN: 978-1429204941

6th edition

Authors: K. Peter C. Vollhardt, Neil E. Schore

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Question Posted: May 12, 2020 02:58 AM

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Glucose reacts with ammonia in the presence of a trace of acid to give predominantly -D- glucopyranosylamine.

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The detailed mechanism is given belowOnly C1 hydroxy...View the full answer

Organic Chemistry structure and function

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