(a) So, the absolute R and S
configuration with their IUPAC name of the given molecule including
their numbering of the group (on the priority basis) and the
direction of rotation is given as below:-

(b) So, the absolute R and S configuration with their IUPAC name of the given molecule including their numbering of the group (on the priority basis) and the direction of rotation is given as below:-

(c) So, the absolute R and S configuration with their IUPAC name of the given molecule including their numbering of the group (on the priority basis) and the direction of rotation is given as below:-

4. (4 points) Assign absolute configuration (R or S) to each stereogenic center of the molecules...
3. (4 points) Assign absolute configuration to each stereogenic center(s) in each molecule, draw an enantiomer of each molecule, and then indicate if each molecule optically active or optically inactive. (a) (b) Он но. но- Он CHS enantiomer enantiomer
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 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
15 uestion 25 Assign the Ror S configuration to each stereogenic center in the Fischer projection below. CHO HTH a+H H- OH CH3 O R, S, R R, R, R OOOOO S, S, S SRS S, S, R
Assign R/S configurations to each chiral center in the following molecules. Clearly label the stereocenter and show your priority ranking. If no chiral centers exist, write "achiral." (15 pts) GEHICH ANTICHE VSH он "CH, HjC NH2 OH
3. R, S Configurations Assign R, S configurations to each indicated chirality center in the molecules below. 14. OH 15. COOH ---H CH NH2 HỌN H -CH3 HO alanine norepinephrine - 18. 16. HOC / OHH HV CH; НС . H7 HO COH CH2 dihydrocarvone tartaric acid
4. Assign R or S configuration at each chiral center below. (2 points) CIH
4. (26 points) Identify each chiral carbon in the molecules below with an asterisk (*) and assign R or s absolute configuration to each chiral carbon. Then, state (in the box provided) whether the molecules are enantiomers, identical, diastereomers, or not related. Hint: if it looks like a Fischer projection then it is a Fischer projection. ...1111 O піон аnd and .Ley O Era o C CHO CH,OH C. H oH and OHCH IH Сн,он
Question 1: Assign the absolute configuration of the chirality center as R or S. ОН Answer: Q:2. Which of the following is the correct IUPAC name of the following structure? A. (S)-3-ethyl-2-methyl hexa ne (R)-3-ethyl-2-methyl hexane (S)-3-ethyl-2-methylpentane (R)-3-ethyl-2-methyl pe ntane В. Answer:
please help with both questions
Clearly assign priorities ( 1-4) for the substituents attached to the mark following molecules. (You do NOT need to determine R or S. Just assign priorities.) ed chirality center in each of the 1. он NH2 2. Circle (or ighlight) all chirality centers in a derivative of progesterone, a cortisone like molecule (shown). Make sure locate all the H's on the molecule first. но- он OH
Clearly assign priorities ( 1-4) for the substituents attached...