Add The substituents in the proper locations on the chair confirmations for each of the following cyclohexanes and the ring inversion compounds 5. ก
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- just part c thanksQ8. Draw the two possible chair-like conformations of compound 1. Using the Çabo LAgld erelog priority rules, assign the absolute stereochemistry to each stareogenic centre contained in compound 1. NH2 'F 1Predict the Ma Show the correct stereochemistry when needed!! Ph NH3 CI substitution H3 + NH3 NH3 P
- Do not use chatgpt. Thank you!Starting from the wedge-and-dash structure below (sighting down the indicated bond), rotate the back carbon to provide the structure in the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded. H H|||| Br H₂C Br H CH₂ Edit Newman Projection CH3 CH3Q7. Using the Cahn-Ingold-Prelog rule, assign the absolute stereochemistry to each stereogenic centre in compounds a-d, and determine whether they are chiral or not. a) b) OH OH H3C CH3 H3C CH3 NH2 c) d) OH H -0 H- H H3C* *CH3 OH OH ОН
- Draw the best chair conformation of trans 1-t-butyl-3-methylcyclohexane.8. The anti-formation of (5)-3-phenyl-2-butanone is included. Draw the attack produce of NaBHa by the face if of this conformation.3 13. Which Newman projection represents the least stable conformation for cis-1-t-butyl-4- methylcyclohexane? B D H