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- In the box below draw the tetrahedral representation of the R enantiomer of the amino acid valine, CH3CH(CH3)CH(NH2)CO2H.WHAT IS THE. RIS CONFIUURATION RELATIONSH IP? Br он VS HO Br.I need help calculating the binding constant and the free energy of binding Base Pairs – A & C 5 ml each Temperature, (°C) 25.00 [A], (M) 0.0441955 [C], (M) 0.0441955 [AC], (M) 0.00580452 Base Pairs – A & T 5 ml each Temperature, (°C) 25.00 [A], (M) 0.00163564 [T], (M) 0.00163564 [AT], (M) 0.0483644
- 8. Explain the following observations: RO™ RCOO, PhO", or RS OCH₂CH₂COOR PhOCH₂CH₂COO™, RCOOCH₂CH₂COO™, RSCH₂CH₂COO™ or4. [a] What can one conclude regarding the nature of the transition state structure for the following cases [i] AS *> "tighter" or "looser" in the transition structure than at the start? > 0, and [ii] AS +<0? In particular, is the transition state structureWhich of the Allwing Paren thesis) has the highest molor heat Cupacity a) Glyeine (97A) 6) Alanıne (121 A) f Leucine (1AI A) Phunylalanıne (228 n") S Tryptophan (204 A) Omino aud residues (accessible surfaa area in In water?
- 6. Fully explain the following regioselectivityDraw the structure of a meso compound with the formula CgH18. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. Ⓡ Sn [F ? ChemDoodleWhich of the following set of molecules is IR active? * HСІ, 02, Н20 O N2, CO, NH3 О СHЗСH20Н, Н2, Н20 O NH3, H20, PCI5
