If the following monosaccharide underwent cyclization to form a furanose, which of the following is one of the possible structures that would be seen? Н HO CH₂OH Н ОН CH₂OH :0 A -OH -Н OH CH₂OH ОН ОН CH₂OH CH₂OH ОН -0. В ОН ОН CH₂OH OH CH₂OH OH с ОН OH ОН CH₂OH OH D OH ОН
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- 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 NThe 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 онRaffinose (see prev. question for structure) is not digestible by humans yet is found in foods we eat all the time like beans, cabbage, brussels sprouts etc. What 2 human digestible compounds can Raffinose be broken down into? Just as a side note, Raff is NOT digestible by us, but our helpful gut bacteria break it down for us into the 2 compounds that are the answer to this question. O a-D-glucose O B-D-fructose sucrose a-D-galactose Lactose maltose
- Write the name for the trisaccharide depicted below (for example, of the form a - D - xylofuranose). Be sure to include if the sugars are in the pyranose or furanose conformations in the name and include the linkages between sugars (for example, (2 - - > 4)). CH₂OH ОН OH н ОН -CH₂ H\H ОН н н ОН CH2OH н ОН но н н ОНWhich 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 HHIIdentify the structure of O-a-D-sorbopyranosyl-(24)-B-D-glucopyranose below. The following structures will help: НО Н ОН х Н H H D-sorbose Н OH CH₂OH Н Н Н OH HO Н H HO H н HO ОН Н н Н О ОН O H Н CH₂OH OH OH н 0 CH2OH Н OH Н H OH Н CH₂OH H ОН Н OH Н Н Н РО OH Н HO OH н н -O CH2O Н O H H OH н Н OH CH₂OH о CHOH H H Н Ко OH H OH Н Н OH Н OH Н OH Н CH₂OH -OCHOH H OH O CH OH Н OH Н Н CH₂OH ОН он OH OH H OH H O OH CH₂OH OH ОН Н O OH OH D-glucose Н ОН Н ОН ОН
- Which of the structures below is that of о-в-D-glucopyranosyl-(1->4)- a-D-glucoругanose CH2OH CH2OH H. OH он H Он OH OH CH2OH HOH2Ć OH он CH2OH CH2OH OH H он H он он CH2OH CH2 OH H OH он OH None of the other structures are correct.Following are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers and the pairs that are epimers. (The sugars shown here are not all of the possible five-carbon sugars.) 1 СНО 2 СНО СНО Н-С—ОН Н-С—ОН Н—С—ОН Н-С—ОН НО —С—Н Н-С—ОН Н- С—ОН НО—С— Н НО—С—Н CH̟OH CH̟OH ČH̟OH в iоchemistry |61 STATE ATION Republic of the Philippines Romblon State University Romblan, Philippines 4 СНО 5 СНО 6 СНО НО—С—Н Н-С—ОН НО -С—Н Н—С—ОН НО -С—Н НО -С—Н H-C–OH Н-С—ОН НО—С—Н CH,OH ČH,OH CH,OHFollowing are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers. CHO сно H-C- OH H-C-OH H-C- OH но-с — н н-с—он но- ČHOH ČH,OH сно CHO Н-с—он но—с— н H-C- OH H-C-OH но—с—н Н-с—он ČHOH ČH,OH сно сно н-с—он но—с —н но—с— н но -с — н H-C- OH но- C-H ČH,OH ČH,OH
- Which of the following is the B-anomer of D-galactose? CHO H-C-OH HO-C-H но-с—Н Н-С—ОН CH2OH CH,OH OH -O, OH OH CH,OH OH он он CH2OH O. OH OH OH OH CH2OH O OH OH OH pone of theseHelp meIn the space provided, draw a Haworth projection for the beta anomer of the following monosaccharide Fischer projection. CHO HO-C-H HO-C-H HO-C-H H-C-OH CH,OH