Rank each set of substituents using the Cahn-Ingold-Prelog sequence rules by numbering the highest priority substituent 1 and numbering the lowest priority substituent 4. Place the number in the blank below the substituent. -CH₂-I -C=N-OH -C-OCH3 -CH=CHCH3
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- 7. Rank each set of substituents using the sequence rules by numbering the highest priority substituent 1 and numbering the lowest priority substituent 4. Place the number in the blank below the substituent. 0= H CH CHCH3 CH= N CH3 CH3= highest priority group, 4 = lowest Rank the substituents shown below in order of Cahn-Ingold-Prelog priorities (1 priority group). -CH2BR -H -OH -CH3Rank the substituents shown below in order of Cahn-Ingold-Prelog priorities (1 = highest priority group, 4 = lowest priority group). -CO₂H 0 -CH=0 O -CH=CH₂ -CH₂CI 0 O
- 1. Assign priorities to these set of Substituents а. -ОН, -СН2CH3 , -CH=CH2 -OCH2CH3 b. -NH2 -NO2 -NHCH3 , -C=N с. -СH2CH3 -CH2SH , -CH(CH3)2 -C=CH d. CH COCH3 -coČCH3 e. -CH(CH3)2 , -C(CH3)3 , -CH2CH(CH3)2 ,-CH2C(CH3)3 f. -OCI , -NHCI -OBr -NHB. End of document IRank the substituents in each of the following sets according to the sequence rules: -OH, -CH2CH3, -H, -CH₂OCH3, -CH-CH2, -CH2NH2, -CH3, -CO2CH3, -Br, E F G H I A B с D Please fill in blanks with letters A-I representing the substituents above them acccording to the sequence rules, from highest to lowest:CH3 HCI CH3 CH3 CH3-CH-OH ZnCl, CH3-CH-CI CH3-C=0 BCD DCB BCD DCB
- Rank the substituents shown below in order of Cahn-Ingold-Prelog priorities (1 = highest priority group, 4 = lowest priority group). -NH₂ -OH -CH3 -FGive the IUPAC name for each of the following: || CH,CH,-0-C-CH,CH, a. b. CH,CH,CH, СН,— С-О-CH,CH,CH,Q8 Conformational Analysis of Cycloalkanes In this question you will look at the conformations of the following molecule: CH3 C В F CH3 D -E A H3C F I II Energy Costs for Interactions in Alkane Conformers: Computed Energy Cost (kJ/mol)* 3.8 Interaction H+H eclipsed H+CH3 eclipsed CH3+CH3 eclipsed CH3+CH3 gauche H»CH(CH3)2 gauche H CH(CH:)2 eclipsed CH3+CH(CH3)2 gauche CH3+CH(CH3)2 eclipsed HeC(CH:)3 eclipsed CH3+C(CH3)3 gauche CH3+C(CH:)3 eclipsed H+I eclipsed I+CH3 gauche I+CH3 eclipsed "Values computed with Gaussian09 using B3LYP/6-31G(d) for structure optimization and B3LYP/6-311+G(2df,3p) for the conformation energy. The calculations were performed in the gas phase (no solvent). *This result for t-butyl is a bit peculiar given that the value is less than that for isopropyl, but there is an explanation that I can tell you about in office hours! 4.8 12.6 3.7 (0.0) 3.1 3.6 17.3 2.8 13.6 18.7 6.7 1.2 15.5 Steric Strain in Monosubstituted Cyclohexanes: 1,3-Diaxial strain Y (kJ/mol)…
- For each pair of substituents, select the higher priority substituent according to the Cahn-Ingold-Prelog system. B. Which substituent has higher priority? A. Which substituent has higher priority? H2 CH3 H2 .C. CH ČH3 H2 CH3 -CH Br H2 CH2 C. Which substituent has higher priority? CENRank the substituents shown below in order of Cahn-Ingold-Prelog priorities (1 = highest priority group, 4 = lowest priority group). -OCH3 -CH=0 -CH2OH -BrFor the molecule given, prioritize each substituent on the stereogenic carbon, and assign absolute stereochemistry. Part: 0 / 2 Part 1 of 2 Cl Assign priority to each substituent. -CH,O- - CH3 - CH₂0¹8- - C1 (Choose one) ▼ (Choose one) (Choose one) ▼ (Choose one) ▼ X