1. Assign R or S configuration on the chiral center(s) in each of the given molecule H =CH₂ сн,сня
8. Assign R or S configuration on the chiral center(s) in each of the given molecule Cl 牖. a) H CH2CH3 HO d) c) f)
designate the R/S configuration for any chiral centers нсн, но, сня H.CH, H, CH3 Но, | | H NH20 Кн 23, HC NHA 24. нсн, нсна H CH3 нон Дн 26 но сн, .. .CH OH нд но со Р o . 28 ноги нас < HO 29. Но LOH не 30.
Assign the R/S configuration to each chiral center below. If you have difficulty, try building a molecule.
4. Assign R or S configuration to each chiral center in each of the following molecules (A-D). Which are enantiomers and which are diastereoisomer? Hint: redraw the molecules if it makes it easier to visualize or use a modeling kit. H H A В CH Br Hас, Br 'CHs Нo Hас H он Br Br D CHз Hас Н. "CHз но Он CH3
Determine if the following molecule is chiral and then assign R or S configuration to the chiral carbon(s):
1. (23 pts.) Label each stereocenter (chiral center) as Ror S. Label each molecule as chiral or achiral. CH ен-он H- CH3 . Он CH2OH Сн,он h) н он В ньон нон НО-Б-н ен,он но- н H-LOH CH OH
4. Consider the molecules shown below. Assign the R/S configuration to each chiral center below. If you have difficulty, try building a molecule. (4 points) он Br н NH2 Br
4. Assign R or S configuration at each chiral center below. (2 points) CIH
Circle each chiral center and determine if it is R or S configuration ОН HHн H- CH3 он
2. Mark all stereocenters with an asterisk (*) and assign the configuration (R or S) for each. Also write whether the molecule is chiral, achiral, or meso (3 pts each) H CH2OH b. c. tch Br Сн, 3. Name the following compounds (2 pts each) Br b.