H. H- OH H OH но OH CH2OH

Q: Draw both pyranose anomers of each aldohexose using a three-dimensional representation with a chair…

A: The following rules should be obeyed to convert Fischer projection to Haworth projection- Draw a…

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: Convert the Fischer projection to the Haworth projectión of the a-py. appropriate positions. The…

A: In biomolecules, the Fischer projection formula of the carbohydrates can be converted into the…

Q: Label each Haworth projection as an α or β anomer and convert the Haworth projection to a…

A:

Q: 2) Part 1: Draw D-glucose in its proper Fischer Projection (using the template below). Part 2: Draw…

A: Given

Q: Label each Haworth projection as an α or β anomer and convert the Haworth projection to a…

A: The anomer in which the alkoxy or hydroxyl group on the anomeric carbon is pointing downward is…

Q: СНО H ОН H- ОН HO: -H- H- OH CH2OH

A: Step 1  We have ;                                          which is L-Glucose . It is an L sugar   →…

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: Draw the products formed when ß-D-galactose is treated with each reagent.a. Ag2O + CH3Ib. NaH +…

A: a.

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

A:

Q: Treatment of D-glucose with NaBH4 gives an alditol A. What L-aldohexose also yields A when treated…

A: Step 1: When aldohexoses react with NaBH4 undergo reduction to form corresponding alditol. When…

Q: Treatment of D-glucose with NaBH4 gives an alditol A. What Laldohexosealso yields A when treated…

A: When aldohexoses react with NaBH4 undergo reduction to form corresponding alditol. When glucose is…

Q: Draw the products formed when β-D-galactose is treated with each reagent. a. Ag2O + CH3I b. NaH +…

A: The OH groups of monosaccharides on reaction with base and an alkyl halide convert into ether. A…

Q: 2. Draw the Haworth projection of the a-anomer CHO HO-H HO- H- H- H OH CH2OH

A: to form a cyclic structure using hetro atom

Q: What monosaccharides are formed in the Kiliani-Fischer synthesis starting with D-xylose? HCFO H--OH…

A: -> Kiliani-fischer synthesis involves addition of cyanide ion to an open chain aldehyde which…

Q: Draw both pyranose anomers of each aldohexose using a three-dimensional representation with a chair…

A: The structure of D-sugar is given by, The steps for the conversion of Fischer projection of D-sugar…

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: 1. Why is "A" the major acetal formed when d-erythrose reacts with H2SO4 and acetone?

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Draw the following monosaccharides, using chair conformations for the pyranoses andHaworth…

A:

Q: Convert attached aldohexose to the indicated anomer using a Haworth projection.

A: Given aldohexose is

Q: On the templates, draw a Haworth projection of the a-isomer and ß-isomer of the sugar shown. (b)…

A:

Q: Answer the following questions about monosaccharide A.a. Draw the α anomer of A in a Haworth…

A: a) The α anomer of A in a Haworth projection has to be given,   The given compounds, The structural…

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

A: When given monosaccharide reacts with water, it forms open chain structure. All the up OH groups…

Q: 3-Fucosyllactose is another HMO found in breast milk. (a) Locate any acetal and hemiacetal. (b) What…

A: The Human Milk Oligosaccharide (HMO) 3-FL (3-Fucosyllactose)the most abundant fucosylated HMOs, and…

Q: What product is formed when D-arabinose is treated with each r (a) H,, Pd; (b) Benedict's reagent?…

A:

Q: What is the name of compound A? CHO H- HO- H- -OH -H -OH CH₂OH A A. D-ribose B. L-talose C.…

A: What is the name of the compound A ?

Q: Label attached Haworth projection as an α or β anomer, and convert the Haworth projection to a…

A: The given molecule is D- Allose. In the given structure, the CH2OH and the anomeric OH group are cis…

Q: Answer the following questions about the eight aldopentoses: a. Which are enantiomers? b. Which are…

A: a.  The aldopentoses are eight in number which consists of D and L form of ribose, arabinose, xylose…

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

A: a. Compound iv is having keto functional group. This keto group is oxidized by Tollens reagent. b.…

Q: Draw the structure of melezitose (either in Haworth or in conformer):…

A: The required Haworth conformation structure of melezitose…

Q: Consider the following compounds: CHO НО -H НО -H -OH -OH CH OH НО HO-H CHO но-+-н Н Н- н-он OH…

A: from the given compounds we have to identify the structure which is an alpha anomer  has an L…

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: How many chirality centers are contained in (a) the aldotetrose and (b) the ketopentose just given…

A:

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: Label attached Haworth projection as an α or β anomer, and convert the Haworth projection to a…

A: In an α-anomer, the CH2OH group and anomeric OH group are trans to each other. Therefore, the…

Q: Convert each compound to a Fischer projection, and label eachstereogenic center as R or S.

A: In Fischer projection, the horizontal bonds are drawn on the wedge that is above the plane while the…

Q: Draw the Fischer and Haworth Projection of the following   Fischer Haworth D- glucose     D-…

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Q: Shown below is the Fischer projection of D-ribulose. Which of the choices below would be a proper of…

A: we have to select the structure of alpha D ribulose

Q: Using Fischer projection structure where no cyclization took place, what product/s formed when…

A:

Q: Label each Haworth projection as an α or β anomer, and convert the Haworth projection to a…

A: The structures are given below along with the answers.

Q: Draw both pyranose anomers of each aldohexose using a threedimensionalrepresentation with a chair…

A: The given structure is,

Q: Convert attached aldohexose to the indicated anomer using a Haworth projection.

A: Carbohydrates are the component of food. They are also called sugars. Aldohexoses are the…

Q: Convert the following Haworth projection to the acyclic form of thealdohexose.

A: Haworth projection is the pyranose form that is the cyclic form. To convert the Haworth projection…

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: 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: 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…