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- Show how the Cahn-Ingold-Prelog sequence rules are used to assign the configuration of the stereogenic centre as either R or S. Select the correct answers from the drop-down boxes. Be sure to answer all parts. Priority (select) Priority (select) V Y V V ?v 'C MeOC 'C ¹H 'C SC Configuration (select) 'H ¹H Priority (select) Priority (select)Polynucleotide H2N. N. HN. :ö: DNA P=0 NH Melphalan Draw the product of this reaction by following the arrow pushing guide above. What kind of reaction (substitution or elimination) is this? vhich one is the nucleophile? Describe the mechanism of the reaction (Sn1 or Sy2 or E1 or E2? Why?Identify the major organic product
- Please don't provide handwritten solution ..... How do you draw the initiation, propagation, and combination termination of Methyl Methacrylate which is CH2=CCOOCH3?(b) Redraw and complete the diagram below to illustrate nucleophilic attack by the N7 atom of a guanine base on a prototypical alkylating agent R-L, where "L" is a leaving group. R Zum N ΝΗ NH₂ -L ?a) Propose a synthesis using a maximum number of 5 synthetic steps, for the dipeptide NH2-ILE-ASP-COOH. Explain your choice of protecting groups
