Label each stereogenic C centre in compounds 1-8 as R or S (remember to label centres in multistriatin);Classify where possible as syn or anti diastereomer
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Label each stereogenic C centre in compounds 1-8 as R
or S (remember to label centres...
R / S stereocenters 8. Try R 1 S stereocenter! Label each group on the stereocenter...
R / S stereocenters
8. Try R 1 S stereocenter! Label each group on the stereocenter as 1, 2, 3, or 4. First look at the 4 atoms directly bonded to the stereocenter (chiral carbon). For tiebreakers, use the 3 bonds (other than bond to stereocenter) that are on each of the "tied" carbons. 4 atomsTiebreaker Rank (3 other bonds) Br Once you have rankings, Make sure #4 is pointed away, then see which direction the 1 to 2 to...
Determine the oxidation number of each clement in the R S following ions or compounds. 0...
Determine the oxidation number of each clement in the R S following ions or compounds. 0 -2 (a) BO, (d) Cal (b) CO2- (e) H SIO GC-+ 30-2 c) - HSO- (pl GFS-1 d Cast2 Haul e_Hat Sixt6 03-22 $_H=+1 $216-02-2 7. Which two of the following reactions are oxidation reduction reactions? Explain your answer in each case Classify the remaining reaction. uds) (a) Zn(s) + 2 NO, (aq) + 4H,O'faq) → Zn2+ (aq) + 2 NO 8) + 6H2O(C)...
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8....
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8. Label the indicated atoms in the structure below as 1º, 2º, 3º, or 4º. PB A A B co 9. Draw Newman projections for the day-diethylane about the C4CS bond, Circle the most stable conforme if you need additional space, please feel free to the backside of this paper 10. Draw the chair conformation and ring-flip for the given compound. Calculate the sterie strain...
R / S stereocenters
8. Try R 1 S stereocenter! Label each group on the stereocenter as 1, 2, 3, or 4. First look at the 4 atoms directly bonded to the stereocenter (chiral carbon). For tiebreakers, use the 3 bonds (other than bond to stereocenter) that are on each of the "tied" carbons. 4 atomsTiebreaker Rank (3 other bonds) Br Once you have rankings, Make sure #4 is pointed away, then see which direction the 1 to 2 to...
Determine the oxidation number of each clement in the R S following ions or compounds. 0 -2 (a) BO, (d) Cal (b) CO2- (e) H SIO GC-+ 30-2 c) - HSO- (pl GFS-1 d Cast2 Haul e_Hat Sixt6 03-22 $_H=+1 $216-02-2 7. Which two of the following reactions are oxidation reduction reactions? Explain your answer in each case Classify the remaining reaction. uds) (a) Zn(s) + 2 NO, (aq) + 4H,O'faq) → Zn2+ (aq) + 2 NO 8) + 6H2O(C)...
6. Provide the IUPAC names for the compounds below Name: 7. Draw the following: cis-1-isobutyl-2-propyleyclopentane 8. Label the indicated atoms in the structure below as 1º, 2º, 3º, or 4º. PB A A B co 9. Draw Newman projections for the day-diethylane about the C4CS bond, Circle the most stable conforme if you need additional space, please feel free to the backside of this paper 10. Draw the chair conformation and ring-flip for the given compound. Calculate the sterie strain...
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