Question: could someone explain why these are wrong? A. For the following atachmsents, which would have the highest priority in the Cahn-Ingold-Prelog rules: (a) CCH (ab)
A. For the following atachmsents, which would have the highest priority in the Cahn-Ingold-Prelog rules: (a) CCH (ab) COOH, (c) NH2 or (d) NO2 B. Which of the following cyeloalkanes has the highest (best) aqueons solubility: (a) cyclobatane, (b) cyclopentane, or (e) cyclohexane C. Which of the following cormpounds contains a non-carbon chiral center: (a) (b) (c) D. Compound A has a specific rotation of -16.0 . If the observed rotation for a 400 , mg sample of Compound B dissolved in 6.0mL of acetone is recorded at +16.0 , what is the likely composition of the solution: (a) diastereomer of Compound A,(b) enantiomer of Compound A, or (c) racemic mixture 5. (4 points each) Determine the relationshap between eoch of the following pairs of molecules: Identical Compounds Conformations Constitutiopar isomers Diastereomers some for mwia different Enantiomers Identical Compounds. Conformations Constitutional isomers Diastereomers Enantiomers A. For the following atachmsents, which would have the highest priority in the Cahn-Ingold-Prelog rules: (a) CCH (ab) COOH, (c) NH2 or (d) NO2 B. Which of the following cyeloalkanes has the highest (best) aqueons solubility: (a) cyclobatane, (b) cyclopentane, or (e) cyclohexane C. Which of the following cormpounds contains a non-carbon chiral center: (a) (b) (c) D. Compound A has a specific rotation of -16.0 . If the observed rotation for a 400 , mg sample of Compound B dissolved in 6.0mL of acetone is recorded at +16.0 , what is the likely composition of the solution: (a) diastereomer of Compound A,(b) enantiomer of Compound A, or (c) racemic mixture 5. (4 points each) Determine the relationshap between eoch of the following pairs of molecules: Identical Compounds Conformations Constitutiopar isomers Diastereomers some for mwia different Enantiomers Identical Compounds. Conformations Constitutional isomers Diastereomers Enantiomers
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