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PtichkaEL [24]
3 years ago
14

For the α anomer of a D-sugar, the anomeric hydroxyl in a Haworth projection Group of answer choices has an upward projection (o

n the same side as the terminal CH2OH group). has a downward projection (on the opposite side from the terminal CH2OH group).
Chemistry
1 answer:
astra-53 [7]3 years ago
5 0

Answer:

The answer is "choice 2".

Explanation:

Its glycosidic fruit juice facility would be a chromosomal hydrogen bond and an aldehyde (or acetone) team generated from the intramolecular creation of the acetals (or ketal).

Its two heterocycles created at the anomeric core from of the 2 potential stereochemical are named anomers, that's why choice "has a downward projection (from terminal CH2OH party on the opposite side)" is correct.

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