Question questions. Answer the following A) Compare and contrast triglycerides in fat and oils? Draw an example of each B) Examine the isomers below. What makes them isomers of each other? Draw the disaccharide that can be made by linking these sugars and
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- Analyze the following biomolecule using the criteria listed below. Be sure to be clear, concise, and complete with your responses. 1. What class of biomolecules does this compound belong to? Explain why. 2. Break this compound down into its components and clearly identify each section of the molecule by labelling (circle or draw an arrow to) its backbone structure, all functional groups, and all biomolecules in the structure. 00-P-O NH3 HODescribe the important biochemical properties of carbohydrates and why carbohydrates would be considered polar molecules. A▾ B I X @ F 7Gentiobiose (D-Glc(ß1→6)D-Glc) is a disaccharide found in some plant glycosides. Draw the Haworth structure of gentiobiose based on its abbreviated name. Show all multiatom groups using the groups tool. Show stereochemistry using wedge (upward) or dash (downward) bonds.
- Draw the amino acid product that results from a transamination reaction involving pyruvate and glutamate, shown in the image below. Draw the product as it would occur at the pH of most body fluids, including all charges. You do not need to draw the other product of the reaction. O NH3 3D CH3-C-C-o-+ 0-CH-CH CH2-C-0--→? pyruvate glutamate Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Include all hydrogen atoms and charges. > View Available Hint(s) CONT. H. N. NV CI Br 1] -C- C1 SIHere is still another lipid-related question. a. Draw the structure of a soap molecule, derived from a myristic acid triglyceride. No sticks. You CAN bunch the CH2 groups together. b. Write the COMPLETE AND BALANCED reaction for your soap reacting with hard water containing Fe*. NO STICKS! c. Describe what you would see if you used a detergent (rather than a soap) in the presence of Fe*. The more detail you give, the more points you will earn. No reactions are needed here.BIOCHEMISTRY LECTURE SOLUTIONS AND ANSWERS SHOULD BE HANDWRITTEN. The following structure is sorbose CH2OH 1. Is this D or L sorbose? C = O | Н-С-ОН 2. Is this a ketose or an aldose? 3. Which carbon atoms will cause it to cyclize? НО - С - Н 4. Draw the boat conformation of no. 3. Н-С-ОН 5. Draw the chair conformation of no. 3. CH2OH 6. How many stereoisomers does sorbose have? 7. Draw all the L isomers of this sugar. 8. Group the L isomers as enantiomers and diastereomers. 9. Draw B-D-sorbofuranose. Draw B-D-sorbofuranosyl(2-1) B-D-glucopyranoside. Is this a reducing sugar? What would be the probable function of this disaccharide, structural or storage?
- OFF Draw with Add Pen Trackpad Q1: Complete the following table: (A.C 1.1, 1.2) Molecular Formula Molecule Structural Formula o-d=0 CH2 CH3 Variable H. --H-N H. H. H 1-- Amino Acid C2H5NO2 (Glycine R=H) Glycerol H H . H H HH H H но . H H H H H HH a-glucose glish (United Kingdom) MacBook ProBIOCHEMISTRY LECTURE SOLUTIONS AND ANSWERS SHOULD BE HANDWRITTEN. . The following structure is sorbose CH2OH C-0 C = O Н-С-ОН ize? НО - С - Н Н-С-ОН 5.1 CH2OH 6. F'- 7. Draw all the L isomers of this sugar. 8. Group the L isomers as enantiomers and diastereomers. 9. Draw B-D-sorbofuranose. Draw B-D-sorbofuranosyl(2–1) B-D-glucopyranoside. Is this a reducing sugar? What would be the probable function of this disaccharide, structural or storage?BIOCHEMISTRY LECTURE SOLUTIONS AND ANSWERS SHOULD BE HANDWRITTEN. : The following structure is sorbose CH2OH C = O Н-С-ОН НО - С - Н 4. Draw the boat conformation of no. 3. Н-С-ОН 5. Draw the chair conformation of no. 3. CH2OH 6. How many stereoisomers does sorbose have? 7. Draw all the L isomers of this sugar. 8. Group the L isomers as enantiomers and diastereomers. 9. Draw B-D-sorbofuranose. Draw B-D-sorbofuranosyl(2–1) B-D-glucopyranoside. Is this a reducing sugar? What would be the probable function of this disaccharide, structural or storage?
- AMINO ACIDS 1. Write the tripeptide structure for: val-ser-cys. 2. Write the reactions for: phe + serModify isoleucine to show the predominant forms at pH 1, 7, and 13. Isoleucine has, values of 2.4 (carboxyl group) and 9.7 (amino group). Isoleucine at pH 7 Isoleucine at pH 1 CH3 CH₂ + H₂C CH +H₂N- C H Incorrect Isoleucine at pH 13 Incorrect H₂C H₂N- CH₂ | CH₂ CH c- C H 0 ĭ Incorrect H₂C +H₂N-For disaccharide b, give the monosaccharide units produced by hydrolysis, the type of glycosidic bond, and the name of the disaccharide, including a or 8. CHOH CH,OH H. OH H. HO Match the words in the left column to the appropriate blanks in the sentences on the right. Reset Help galactose and fructose When the disaccharide is hydrolyzed, the monosaccharide units that are produced are two molecules of fructose two molecules of glucose The type of glycosidic bond shown for the disaccharide in thin part is 8-1,4 The name of the disaccharide including a or A in B-1,2 a-1,4 a- 1,2 a-lactose B-lactose a-maltose B-maltose