Organic Chemistry
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Suggest a suitable mechanism to show the formation of methyl ether at any one of the hydroxy groups of methyl α-D-galactopyranoside by treatment with dimethyl sulfate and sodium hydroxide.
What product will be formed when the given sugar reacts with an excess of methyl iodide in the presence of Ag2O?
What product will be formed in the reaction of the given monosaccharide with an excess of methyl iodide in the presence of Ag2O?
What product(s) would you expect when α-D-glucopyranose reacts with excess CH3I and Ag2O?
What will be the product of the reaction shown below?
Give the product that will form from the reaction shown below.
Draw the structure of D-psicofuranose after it reacts with excess CH3I and Ag2O.
Draw the structure of methylated D-psicofuranose after it is hydrolyzed in dilute acid.
After methylated D-sorbofuranose is hydrolyzed, what do the results imply about the relationship between D-sorbofuranose and D-sorbose?