Hycz 12 40-C-14 4 40-C-1+ 15. CH₂Olt 1. (2 pt) Draw the Haworth projections of the a-furanose and pyranose forms of the sugar shown below. Pay close attention to D-/L- and the correct anomeric carbon for the furanose. Olt diasterio mer = 2+

Convert the Fischer projection to the Haworth projection of the a-furanose form by moving the substituents to the appropriate positions. The anomeric carbon is shown. CH₂OH -H Cyclization -OH -OH CH₂OH Answer Bank CH₂OH HO- -H H- OH

Which of the following is an anomer of B-D-gulopyranose? O O го ОН H ОН H ОН H H ОН CH₂OH -II- H H ОН ОН CH2OH H ОН ОН CH2OH О 0. H CH2OH то Н H H ОН H H - о H ОН ОН H ОН H ОН ОН H О ОН ОН H N

Which of the following is an anomer of a-D-galactopyranose? CH,OH он он он H он ÇH,OH OH он H он H он ÇH,OH он H. H OH он ÇH,OH OH он он он HHI

where is a reducing end in this image? I initially thought it'd be on the middle oxygen connecting the lactose molecules since it's the only reducing sugar, but that was incorrect for some reason.

During the process of synthesizing palmitate (C16), an acyl ACP __________. For the sake of this question, don’t treat acetyl ACP or malonyl ACP as an acyl ACP; assume the acyl ACP is a product at least 4 carbons long. Choose ALL that apply. (A) can be condensed with malonyl ACP to produce a Cn+2 b-ketoacyl ACP (B) is formed from the reduction of a trans D2-enoyl ACP(C) is a product of acetyl transacylase(D) is reduced by NADPH (E) is a substrate for b-ketoacyl synthase(F) can be condensed with acetyl ACP to produce a Cn+2 b-ketoacyl ACP

Use the two Fischer projections shown below to draw the Haworth projection of these two sugars linked by an a(1-2) linkage, with the ß isoform of the ketohexose. H H ㅎ HO H H OH OH ОН Н НО CH₂OH 애,애애 OH CH₂OH OH H OH OH OH I OH CH₂OH OH OH OH Eng са CH2OH CH2OH OH OH ОН ОН CH₂OH Н OH Н Н OH Н T I CH₂OH CH₂OH OH OH OH CH₂OH CH₂OH Н CH₂OH CH₂OH ОН OH OH НО OH H Н OH CH₂OH

The anomer of a-D-glucopyranose is CH:OH он ÓH CH2OH он он он он CH,OH он он он он CH,OH он OH он ÓH ÇH;OH он он он он

please help with this question

Modify the mannose structures provided to show the structure of a disaccharide formed from two mannose uni 1-6-ẞ-glycosidic linkage. CH₂OH CH₂OH H OH H OH H H OH OH OH OH OH H OH H H H H H