Learning arget 8 Criteria for satisfactory score Conversion between projections must be correct (represent the same molecule). Stereoisomeric relationship must be correctly identified. Explanation must be logical and in agreement with the stated stereoisomeric relationship. Tasks 1. Convert the bond-line structure of isomer B (Figure 5) to its Fischer projection. 2. Determine the stereoisomeric relationship between compounds in Figure 5 and explain your choice. CH3 H-NH2 NH, 0 -NH2 H3C, H- CH3 H +CI NH, ČI `CH3 isomer A isomer B Figure 5: Isomers

E. Draw the two ring interconversion structures each for cis and trans 1-cyclopropyl-2-ethylcyclohexane and rank all four according to stability (code: 1 = most stable to 4 = least stable). Be sure to also draw all hydrogen atoms and justify your four stability choices.

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Convert the following to a Newman projection using the template provided. Name the compound including R or S configuration. ļ F F

Your document is saved. Click CONVERT A. Conjugated Molecules I I) Designate each molecule as conjugated or not conjugated. For conjugated molecules, circle the atoms that are conjugated. HO. NH2 но. HO ... Chat with II) Use the molecule below to answer the following: a) Number of lone pairs 10 Automatic Zoom 2020, LegalSimpli Software, LLC. a subsidiary of Conversion Labs, Inc., All rights res + t Page: 1 of 2 MacBook Pro