(a) Explain why the oxygen at C1 of an aldopyranose can be methylated so much more easily...
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(a) Explain why the oxygen at C1 of an aldopyranose can be methylated so much more easily than the other oxygens in the molecule.
(b) Explain why the methyl ether unit at C1 of a fully methylated aldopyranose can be hydrolyzed so much more easily than the other methyl ether functions in the molecule.
(c) Write the expected product(s) of the following reaction.
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1 The water molecule is ejected from 1position in an aldopyranose in a given Scheme after protonatio...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
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