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CARBOHYDRATES POST-LAB QUESTIONS [52] 19. Review the Fischer structures of D-galactose, D-glucose, and D-mannose Identify each...
T. How many stereoisomers of beta-D-glucopyranose exist (including itself)? a. 4 e. too many to consider b. 8 с. 16 d. 32 onsider the following Fischer projections and answer the questions: CHO H OH HO H H OH H O ČH2OH glucose CHO CHO H OH Но- СНО н H- OH HO OH HO -н -н H- OH H HO -H HO н- H OH ČH2OH H OH CH2OH OH CH OH allose galactose talose 2. Which pair are not...
D-Glucose is in dynamic equilibrium between the three structures shown below. Choose the form of glucose that best satisfies each of the following characteristics. OPTIONS ARE: alpha-D-glucopyranose, beta-D-glucopyranose, D-glucose (open chain). 1. most reactive form - ? 2. structural unit of disaccharide maltose - ? 3. structural unit of the disaccharide cellobiose - ? 4. structural unit of the polysaccharide glycogen - ? 5. structural unit of the polysaccharide cellulose - ? CH2OH но HO H-C-OH но-с-н н-с-он н-с-он Сн,ОН...
Carbohydrates homework 1. Identify the sugars as aldose or ketose, Lor D, and determine the number of Chiral centers. Сон CHO к он СКО КО- { ой -Н НО Н и о ко ги но И. н 애 CHROM ch, Сон и D Сн оя ь, о H он и к ой ho И 10. И и — ой ch 20h CH₂oh 2. Identify the relation between the structures in each of the following pairs. СКО СКО Си0 Cheon И...
Question 9 15 pts Determine the relationship between each set of structures Set 1: identical Set 2: constitutional isomers Set 3: diastereomers Set 4: diastereomers Set 5: enantiomers 2 OH OH OH e HO... г - 2 ОН ОН ОН Но... 3 ОН Н. СІ НО, CI нс H нс ОН ОН H 5 н- H CHO -ОН ОН CH2OH CHO но- -Н Н- -ОН Сн,ОН Е.
Carbohydrates homework 1. Identify the sugars as aldose or ketose, Lor D, and determine the number of Chiral centers. cv.ok CHO к D ско 1 н- 4 ko ho- M "Т, oly CH₂OH ChooH Chaok И CH₂OH H ой k он ой н ho И no и ой си, ch 20h 2. Identify the relation between the structures in each of the following pairs. с СО со Chow но -И h он lko НЕ OM -v с Р oh -...
35. Enzymatic processing to break down glycogen into glucose occurs at: a. a reducing end. b. a non-reducing end. c. reducing and non-reducing ends simultaneously. d. branch points exclusively. 36. Which furanose is the B anomer of the monosaccharide given by the Fischer projection below? CH2OH 0= но о он a OH но о K он но, HOT о, -н он о. он Он KOH /он но TOH Нон но LOH HO но н но - он но -ОН -н...
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...
Name the following aldoses. (Include in the names the stereochemical designation D or L and, where appropriate, the configuration of the anomeric carbon, alpha or beta. This question is case-sensitive, so capitalize only the D or L.) ball & stick + labels b all & stick + labels The following model is that of an aldopentose: ball & stick - + labels Draw the alpha anomer of the sugar in its furanose form. Classify each of the following sugars. (For...
CARBOHYDRATES POST-LAB QUESTIONS CONT'D 23.Draw the Haworth structure of lactose and explain why this disaccharide gives a positive Benedict's test; make sure to circle the part of the structure that is responsible for the reaction with Benedict's reagent. [5pts) Haworth Projection: (2.5 points) Hemiacetal circled / indicated (2.5 points) CARBOHYDRATES POST-LAB QUESTIONS CONT'D 24. When Benedict's reagent reacts with a reducing sugar, it oxidizes the aldehyde functional group to a carboxylic acid. As seen in the figure below: only a...
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....