For the α anomer of a D-sugar, the anomeric hydroxyl in a Haworth projection Group of answer choices has an upward projection (on the same side as the terminal CH2OH group). has a downward projection (on the opposite side from the terminal CH2OH group).

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.

a) the particles of the chair are strongly held together.