Explain anomer of its pyranose haworth structure

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Please help me right now! I will give you full credit if you answered it correctly. I am confused actually.

1. Starting with d-talose (you can find this in the book or online) draw the \(\beta\) -anomer of its pyranose Haworth structure.

a. How many stereocenters are in its Haworth structure?

b. How do you make the anomeric carbon unreactive?

Reference no: EM13209681

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