Answer the following questions about compound A, represented in the given ball-and-stick model. In a ball-and-stick model, each black sphere represents acarbon atom and each white sphere represents a hydrogen atom.Part 1 of 4Give the IUPAC name for compound A.8-methylnon-1-enePart 2 of 4Draw the skeletal structure for compound A.Part: 2/4Part 3 of 4caDraw the skeletal structure for the product formed when compound A is treated with H, in the presence of a metal catalyst.Part: 3/4Part 4 of 4O: AEDraw the skeletal structure for the product formed when compound A is treated with H₂O in the presence of H₂SO4-Click and drag to start drawing astructure.'b

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Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Identify the type of isomerism exhibited by the following pairs of monosaccharides D-glyceraldehyde & dihydroxyacetone D-glucose & D-mannose α-D-glucose & β-D-glucose d-galactose & l-galactose D-glucose & D-allose A. optical isomers B. Diastereomers C. Epimers D. enantiomers E. Functional Isomers
A) what does the figure illustrate? B) Label the components in the figure pointed by the arrows and briefly mention the bonding partners involved in each case
Provide the precise chemical description (anomer, isomer, and ring form) of the mono-saccharide subunits that are forming the tri-saccharide sugar molecule. Note the indicated numbering of the carbon atoms for the middle and the right subunit. Research the generic name of the tri-saccharide once you have identified the mono-saccharide subunits. Left subunit: Middle subunit: Right subunit: Name of sugar: b) Provide the precise chemical description of the two bonds that connect the sugar subunits?
Identify the catalyst that acts on the boxed structure
For the drug Amlodipine What is one modification could be made to a functional group in order to determine SAR ? Explain why the modification would be useful to determine the SAR.For the drug Amlodipine What is one modification could be made to a functional group in order to determine SAR ? Explain why the modification would be useful to determine the SAR.
2) Consider the following disaccharide which was formed from the breakdown of a polysaccharide found in plant material. ОН Glycosidic linkage: H H OH H H НО H H. OH H. ОН OH H НО H ОН a. Label the glycosidic linkage above in the following format: a/B(# → #) b. Would you expect this disaccharide to have been formed from amylose or amylopectin? c. Describe at least two chemical tests that would give insight into the structure of this disaccharide, assuming you've isolated it and wanted to elucidate the structure from scratch. Include detail on not only the tests you would use but what results you would expect to get given the structure above. Assume you can analyze the structure of any monosaccharide you get from your chemical tests.
Describe the quarternary structure of the enzyme aspartate transcarbamoylase: Dodecamer Monomer Tetramer Hexamer Decamer
With respect to the following compound Gal(816) Glc, what information can we deduce? O the compound is a D-enantiomer. O the glucose residue is the 5 anomer C-6 of glucose is joined to C-1 of galactose by a glycosidic bond. the galactose residue is at the reducing end. O C-6 of galactose is joined to C-1 of glucose by a glycosidic bond.
Consider the structure shown below. он 3 5 CH; O CH, O H CH; O 1 H-N-CH,-C-N-CH;-C-N-CH-C-N-CH-C-N-CH-C-ơ 2 H. H H Fill in the blank with an integer (1, 2, 3, 4, 5..) as shown in the diagram or to represent a specified number. A hydrophilic side chain is indicated by the number
draw all the structures of the tribasic amino acid lysine involved in the equilibrium reactions that would take place during titration against NaOH, starting with the fully protonated form below (draw the R-group in full). H;N+- CH - COOH (CH2)4 NH3+

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