Question

Draw a Haworth projection for each of the following compounds: (a) β\beta-D-Galactopyranose (b) α\alpha-d-Mannopyranose (c) α\alpha-d-Allopyranose (d) β\beta-D-Mannopyranose (e) β\beta-D-Glucopyranose (f) α\alpha-D-Glucopyranose

Solution

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Answered 6 months ago
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Pyranose ring of monosaccharide is hemiacetal that formed in the reaction of the carbonyl group and –OH group from C atom that is four C atom furthest from the carbonyl group.

Groups that are on the right side in Fischer projection are pointed down and groups that are on the left side in Fisher projection are pointed up in Haworth projection. In α\alpha-anomer OH group at anomeric carbon is pointer down and β\beta-anomer OH group at anomeric carbon is pointed up.

Fischer projections are:

'slader'

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