Draw the following monosaccharide in the Beta anomer of the cyclic form 0 C= H- C-...
2. Convert each sugar below to its Haworth form. Draw the alpha anomer for a, the beta for b. CH OH c=0 но-с-н HO-c-H H-C-OH a. CH OH u-u-u-u-u- III н-с-он Сн,он
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН НО- ОН НО ОН о H н ОН HO н НО Н НО H OH О Н H ОН но H НО H Н ОН OH о H Н ОН
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН НО- ОН НО ОН о H н ОН HO н НО Н НО H OH О Н H ОН но H НО H Н ОН OH о H Н ОН
Draw the cyclic structure of the following monosaccharide. Identify the anomeric form that you draw as alpha or beta. Існо на-он HOH НЕОН СН2ОН
1. Below is a monosaccharide in its cyclic (ring) form. OH он Linear form OH a) Is the monosaccharide the a-or the B-anomer? b) Label each carbon with its carbon number. c) Draw the linear form of this monosaccharide with the correct chirality in the box at right. 2. a) Draw the linear form of D-ribose: b) Ribose can form a pyranose ring. Draw an electron arrow on your linear ribose drawing above, indicating which nucleophile attacks which electrophile to...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if a di- or polysaccharide (e.g., B,B-2,3; if there is more than one glycosidic bond, draw an arrow from each label to its corresponding bond). CH,OH CH2OH CH OН но н H Н H Он Н OH н OH Он Н ОН O H Но он b. a. OH H OH CH-OH O H Но ОН Н CH2OH CH2 CH2OH он OCH CH3 Но н...
Classify each monosaccharide by the type of carbonyl group and the number of carbons in the chair - СН,ОН aldo. lect) HO- CH HO– –H HO– –H H- C-OH CH,OH pints CHOH References с н— Но— —ОН —н , сн,он | keo Oose "C
13.34 For each of the following give the monosaccharide units produced by hydrolysis, the type of glycosidic bond, and the name of the disaccharide including a or B: а. СН,ОН СН,ОН НА - 0 H н Он н/ о он н НО Н н ОН НОН СН,ОН - 0 Н НИ / Н ОН Н HO н Оно НОСНО ННО Н СН,ОН OHн
Question 1 (1 point) Choose the reducing sugars (select all that apply): СН,ОН СН,ОН не — о он н ОН НА // Н v H ОН НА у н н н ОН н ОН CH,OH 1 ОНОН а снион и онон н СН,ОН ОН —0, ОН ОН ОН CH2OH -о- слъ We were unable to transcribe this imageQuestion 2 (1 point) Monosaccharide B can be cat Сн,ОН н Дон ү0 р. Н ОН HOCH2 ОН HV СН,ОН В. Г ОН...
Draw the Haworth Projection for the compound represented by this model. also need help answering these questions that go along with the model i included Model 5 (This model does not rotate) Н H CH,OH С C НО НО C Н C с. H ОН) ОН Н (b) Haworth projection formulas of cyclic monosaccharides. View model #5 of the cyclic monosaccharide and answer the following: • Is the ring structure a pyranose (6 sides) or a furanose (5 sides): •...