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 CH316Classify the following substituents as activators and deactivators
- Rank 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 ORank the substituents shown below in order of Cahn-Ingold-Prelog priorities (1 = highest priority group, 4 = lowest priority group). -NH₂ -OH -CH3 -FFor 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
- Assign relative priorities to each set of substituents: a. -CH2CH2CH3 -CH(CH3)2 -CH = CH2 -CH3 b. - CH2NH2 -NH2 - OH -CH2OH c. -C(=O)CH3 - CH =CH2 -Cl -C=NPART 1: For the decalin derivative below please identify the correct Newman projection: Please type your answer as a letter: A, B, C, or D. The answer for PART 1: Н H Н. A B CH3 CH3 Н CH3 CH3 Н အက်သလို လုံး Н. под Н OH CH3 OH H3C Н H3C H₂C H3C H3C Н Н The answer for PART 2: A CH3 OH E C CH3 CH3 OH "CH₂ CH3 H H3C. H3C Н H Н. H.C..... H3C OH OH CH3 PART 2: For the Newman projection below please identify the corresponding decalin derivative with the correct stereochemistry: Please type your answer as a letter: A, B, C, ..., or H. CH3 H B н Н OH F CH3 CH₂ OH он "CH3 OH CH₂ CH3 H3C H H₂C Н H3C Н H C D CH3 SASA SA CH3 H₂C CH3 H₂C" H3C" он CH3 H OH CH3 G CH3 CH3 CH3 ÕH D CH3 CH3 CH3 H H H3C_ Н.С Н CH3 CH₂ H OH H Н CH3Arrange the substituents in order of decreasing priority when determining E/Z stereochemistry of an alkene (i.e., 1 is the highest priority substituent, 4 is the lowest priority substituent). – NHCH3 II - CH v - OCH3 -CH,CI >
- Indicate whether the following double bond is in E or Z configuration and which is the highest priority substituent on each side of the double bond.. NH₂ HS- OZ Configuration: I, CH3 OZ Configuration: I, NH2 OZ Configuration: CH2SH, CH3 E Configuration: CH2SH, CH3 E Configuration: 1, NH2 E Configuration: I, CH3Alcohols can be converted to alkyl chlorides using SOCl2 with complete inversion of stereochemistry. Using curved arrows draw the stepwise mechanism for chlorination of an alcohol. Be sure to include lone pairs necessary to the mechanism steps and any non-zero formal charges.Identify A-D