Draw the product of the reaction shown below at physiological pH (pH = 7.4). Ignore inorganic byproducts. HO Θ H3N O BOC-Leu DCC Select to Draw Q
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- Explain this result: Acetic acid (CH3COOH), labeled at its OH oxygen with the uncommon 18O isotope (shown in red), was treated with aqueous base, and then the solution was acidified. Two products having the 18O label at different locations were formed.Explain this result: Acetic acid (CH3COOH), labeled at its OH oxygen with the uncommon 18O isotope (shown in red), was treated with aqueousbase, and then the solution was acidified. Two products having the 18Olabel at different locations were formed.Draw a mechanism of the reduction of 188Re-perrhenate (Re(VII)) to Re(V) by using SnCl2.
- Give typed explanation 27. Arrange the following molecules in order of increasing acidity CH3CO₂H, H₂O, CH₂=CH₂, CH3CH₂OHa. Propose a synthetic pathway for cis-[NiCl2(CO)2] using trans-effect. b. Propose the methods to differentiate the isomers in between [RhCl2(H2O)4]Cl and [RhCl3(H2O)3].H2O.The following reaction has a ΔSsystem < 0 O2(g) → 2O(g) T or F can you explain why this is false?
- Suppose we aempt the conversion of fumaric acid to deuterated malic acid with BD3·THF,followed by oxidation with D2O2in NaOD(aq). Show all the possible stereoisomers (as Fisherprojections) that may be formed, and draw the mechanistic pathways (showing stereochemistry)that lead to these possible productsShow how the synthetic scheme developed in Problem 23.67 can be modified to synthesize this triiodobenzoic acid X-ray contrast agent.Name the following amine, including R, S stereochemistry, and draw the product of its reaction with excess iodomethane followed by heating with Ag2O (Hofmann elimination). Is the stereochemistry of the alkene product Z or E? Explain.