2) Part 1: Draw D-glucose in its proper Fischer Projection (using the template below). Part 2: Draw B-D-glucopyranose in its proper Haworth Projection (using the template below) H.

Q: An aldohexose would have the functional group A. See first image B. See second image C. -CH3 D.…

A: Functional group is a molecule or group of atoms  that have its own characteristic property…

Q: . Determine the number of stereoisomers possible for a ketopentose

A: Stereoisomerism can be defined as the isomerism in which molecules have the same molecular formula…

Q: Draw the Fischer projection of the product of the reduction reaction of D-Talose at C1C1. Drag the…

A: A Fischer projection or Fischer projection formula is a convention used to depict a stereoformula in…

Q: Shown below is a sugar in chair form. Which Fischer projection gives this same sugar?

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Q: Why are the last two compounds called meso diastereomers? I understand the meso part, but aren't…

A: Enantiomers are the mirror images of each other and mirror images are non-superimposable on each…

Q: What is the configuration of each of the asymmetric centers in the Fischer projection ofa.…

A: If carbon is bonded with four different substituents, then that center is called a chiral center or…

Q: When the only difference between two Fischer projections is that the projection appears to have…

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Q: below backbone. Notate each stereocenter with asterisks.Draw the appropriate wedges and dashes to…

A: Stereocentre has all four different groups which are attached to that group .

Q: D-Mannose and D-fructose are related via two keto-enol tautomerisms. Draw the structure of the…

A: The structure of D-mannose and D-fructose is as follows:

Q: Draw the Fischer projections of the four aldotetroses. Draw the D-sugar on the left and its L-isomer…

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Q: OH OH OH ÓH monosaccharide A

A: We have to find out the most stable chair conformation of monosachharide A is

Q: 6. The Fischer projection for fructose is shown below. Is it a D-sugar or an L-sugar? a. It is a…

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Q: a) Which of the following monosaccharides will react with Tollens’ reagent? Circle all that apply.…

A: The functional groups are the key components of the molecule and are responsible for providing the…

Q: How many stereoisomers are possible for an aldopentose?

A: We know NaBH4 is a reducing reagent it can reduce -aldehyde to alcohol. But since H- can attack from…

Q: a. Draw the enantiomer of D-fructose.b. Draw an epimer of D-fructose at C4. What is the name of this…

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Q: Circle the correct answer in each sentence. Projection 1 is a (boat ; fischer ; haworth ; sawhorse)…

A: Given are two sugar molecules and both are monosaccharide.

Q: Which aldotetrose is the structure shown? Is it d-erythrose, d-threose, l-erythrose, or l-threose?…

A: The given Fischer projection can be sketched on paper as follows:

Q: Draw the β anomer of a monosaccharide epimeric with D-glucose at C2 using a Haworth projection.

A: The anomers can be represented as the cyclic geometric variation of the monosaccharides will be…

Q: 2. Convert the following line structure into a Fischer projection. ОН ОН HO ОН ОН

A: In the Fisher projection,bonds which are below the plane of paper are written on right hand side and…

Q: Given the Fisher projection

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Q: Label the attached stereogenic center as R or S

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Q: ОН ОН H. HO, Но но i) Draw a Fischer projection. ii) From the Fischer projection in question (a) i),…

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Q: Draw Fischer projection of the mirror image (enantiomer) D-robose c. Are these molecules…

A: Enantiomers are the pair of chemical compounds whose molecular structures have a non-superimposable…

Q: A student decided that the configuration of the asymmetric centers in a sugar such as d-glucose…

A: The asymmetric centre's configuration which is farthest from the C=O (carbonyl group) helps in the…

Q: 1. Draw the Fischer projection for a) D-Glucose and b) D-Galactose and their corresponding…

A: 1.Enantiomers are compounds that are non super imposable mirror images of each other.

Q: CH,OH A. Circle the anomeric sugar on the left OH B. Circle the carbon that makes the given sugar…

A: Anomers are cyclic monosaccharides which differ in configuration on one carbon, mostly C-1 in case…

Q: Monosaccharide Structure and Stereochemistry For D-arabinose: Draw an epimer at C3.

A: To find: C3 epimer of D- arabinose

Q: The Fischer Projection of Talose is shown below. Draw its methyl glycoside in its lowest energy…

A: Talose is an aldohexose sugar. It is an unnatural monosaccharide that is soluble in water and…

Q: Draw the α-d-tagatopyranose sugars using Haworth projections:

A: The projection which represents the structural formula of sugar into cyclic form with three…

Q: Draw the ß anomer of a monosaccharide epimeric with D-glucose at C2 using a Haworth projection.

A: The anomers can be described as the cyclic geometric variation of the monosaccharides will be found…

Q: Q4. Draw a Fischer projection of L-psicose. Psicose is the C3 epimer of fructose. Draw a chair…

A: Epimers are carbohydrates which vary in one position for the placement of the -OH group. For a sugar…

Q: a) Which of the following monosaccharides will react with Tollens’ reagent? Circle all that apply.…

A: The functional group belonging to a molecule is an important component that furnishes the…

Q: (a) Is the following stereoisomer of a D or L sugar? (b) In the box provided, draw the enantiomer of…

A: In the Fischer projection of any sugar, The most oxidized atom stays at top as here is CHO group.…

Q: HO

A: If carbon is surrounded by four different group then that carbon is known as chiral carbon.

Q: Draw the chair confirmation of: (a) B-D-mannopyranose (the C2 epimer of glucose) (b)…

A: Pyranose is a 6 membered chain with 5 carbon atoms and one oxygen atom.

Q: A Fischer projection formula of one monosaccharide is given in a box. Which of the following is the…

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Q: d) Draw the structure of the expected product when monosaccharide C undergo mutarotation upon…

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Q: How to Assign R,S designations to  stereogenic center in glucose ?

A: Glucose is a monosaccharide, having formula C6H1206. It is an important simple sugar that circulates…

Q: 3. How many stereogenic centres does the cholesterol have? А. 5 но В. 6 C. 7 cholesterol D. 8

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Q: Please draw the expanded structure of D-altrose and its Fischer Projection (chiral C represented as…

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Q: D-Talose differs from D-Glucose at carbons 2 and 4. ( A. Draw D-Talose on the Fischer template…

A: The open and pyranose structures of D-Talose is as follows;

Q: How many stereoisomers are possible for a. a ketoheptose? b. an aldoheptose? c. a ketotriose?

A: Asymmetric(chiral) centre- It is a molecule having a special arrangement of ligands which is not…

Q: How many d-aldoheptoses are possible? Draw the Fischer projection of one of them and its enantiomer.

A: When the monosaccharide unit has seven carbon atoms, it is termed as heptose. When the heptose has…

Q: How many different aldoheptoses are there? How many are D-sugars? Draw all D-aldoheptoses having the…

A: Aldoheptose is defined as a sugar containing 7 carbon atoms out of which 5 carbon atoms are chiral…

Q: 4.2 Consider the following Haworth projection of monosaccharide A: OH OH OH OH ÓH monosaccharide A…

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Q: Assign R, S designations to each stereogenic center in glucose.

A: The carbon atom which is bonded to four different groups is known as stereogenic or chiral center.…

Q: c. Label the stereocenter at far right on each structure as R or S as appropriate for both anomeric…

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Q: What sugar is the C-3 epimer of d-xylose? . What sugar is the C-5 epimer of d-allose? What sugar is…

A: Hello. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If…