D- gulose 2- epimer is D- idose ( compound Q)
Beta anomer of Q i.e. beta anomer of D idose in Haworth projection is Idopyranose.
Hence structure of beta form of D- Idopyranose is option (b)
--- не тvмvv мина ролет. Compound Q is the 2-epimer of D-gulose. Which of the following...
rt the following Fisher projection into a Haworth projection. Draw only the a anomer. (12 points) CHO но -н нон но o -н bordando o HH -OH CH,OH он contrario si wololo zelo (tiga) audio to 10 mon si batu
Question 2 Identify all D-monosaccharides below: CHO НЕОН НОН Н -ОН НОНЕН CHO НО. -Н НОН НО-НН НО. -Н НО -Н CH2OH ІІ H Н ОН 0= НО-Н НЕОН Н ОН CH2OH CHO Н- -ОН НОН НЕОН НО-Н НЕОН CH OH IV — о Н- НОНЕН Н- ОН НО-Н Н ОН НО НО- CH2OH Ео Н ОН -Н -Н Н. -ОН Н VI CH2OH H ОН 0 Н- НО. -Н НО -Н Н VII Н Нон 0= НЕОН НО-НН НО....
please draw the correct one if not in option and explain. HP Question 2 The Fisher projection below is equivalent to which Haworth structure if the anomer formed is alpha? Cно H- OH но- -H н- Он H- -Он CH-он CH2OH 1) Он Он он Он CH2OH 2) OH Он OH
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
3. (2 pts) Use the Fischer projections shown below to answer the following questions. Reference Sugar a) Which sugar is an epimer of the reference sugar? он ньон Нонн -он -он CH OH b) Which sugar is an enantiomer of the reference sugar? c) Name the reference sugar shown. 1) 2) 5) СОН сон он 9 1 HOH HO- нон } I I но- н нон нон нон CH OH Нон нон нон нон CH OH 5 + } н...
Which is the major product of this reaction? CN 1. Et MgBr 2. acid workup our order on one A B C D A B С D Which compound is a D-isomer? Н. Н. T НО- -Н НО——н НО -Н Н——он Но——Н НО- H -Н он І Н. -он H- -он НО -Н НО -Н CH2OH НО- Н -ОН НО -Н СН2ОН Н. -он НОН Сньон CH OH А B с D OA B Ос D
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): •...
1) SHOW WORK STEP By STEP below is Figure 7-3 Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-allose, (b) D-gulose, and (c) D-ribose at C-2, C-3, and C-4. Answer Epimers differ by the configuration about only one carbon. (a) D-altrose (C-2), D-glucose (C-3), D-gulose (C-4) (b) D-idose (C-2), D-galactose (C-3), D-allose (C-4) (c) D-arabinose (C-2), D-xylose (C-3) (a) D-Aldoses Three carbons Four carbons Five carbons но не HO -OH н-с-он CH, OH D-Glyceraldehyde но-с-н H-C-OH снион D-Threose...
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...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D) below based on carbonyl group and number of carbons (c.8. aldohexose, ketotriose, etc.). Classify them as an antiomer. Indicate the number of chiral carbons for each sugar. Sugar Classification based on carbonyl group and number of carbons Lor D enantiomer Number of chiral carbons н-с-он HO-6-H. н-с-он ін,он CH,OH C=0 HO-C-H н-с-он HO-C-H. ён,он снон c=0 | HO-C-H ін,он H-C-OH CH, OH CD 2....