a) there is no chiral center, hence there will be no R and S assignment.
b ) 2nd and 3rd carbon are chiral centers.
This is a Fischer projection, hence all vertical bonds are going away from the viewer and all horizontal bonds are coming towards the viewer.
Priority order at C2: F > C(Cl,Br) > CH3 > H
The eyesight moves in the clockwise direction but the lowest priority group is not going away from the viewer. Hence the configuration is "S".
Now priority order at C3: Br > Cl > CHF > CH3
The eyesight moves in clockwise direction and lowest priority group CH3 is going away from the viewer. Hence, configuration is "R".
Please note that I am using your numbering as shown in the question and this numbering is not as per the IUPAC system.
c) In this compound the C3 is a chiral center.
Priority order at C3: OH > COOH > CH2 > H
Eyesight moves in the anticlockwise direction. But lowest priority group is not going away from the viewer. Hence the configuration is R.
d) 
assign the R** he R or S designation to each enter by number in The follawing...
3. Assign R or S configuration to the following molecules: Br I F H F H F Br Br -CHE CH=CH2 CH2CH3 CH2CH3 out from H₂C... -CH3 OH CH3CH, -CH=CH2 CH3 CH(CH3)2 H
Designation of Configuration - The R, S System 20 Assign priorities to the groups in each set. (a) --H -CH, OH –CH,OH (0) -CH-CH=CH, CH=CH2 –CH =CH-COOH (c) CH –H COO –NH, (0) CH CHSH –NH -CHO 3.21 Flu
3. Assign R or S configuration to the following molecules: Br F H F . Br F Br -CH CH=CH2 H CH2CH3 CH2CH3 CH3 CH2 --CH3 OH H -CH=CH2 H3C 7 CH3 H CH(CH3)2
3. Assign R or S configuration to the following molecules: Br F Н. F H- Br CH, Br CHECH, H CH2CH3 CH2CH3 CH, CH, -CHE OH H CH=CH2 H3CH2 HY CH(CH3)2 CH 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers Identical d Meso Compounds
3. Assign R or Sconfiguration to the following molecules: Br F н. F Br Br -CH. CH=CH, H CH,CH CH2CH3 CH,CH, -CHE OH -CH=CH2 H3C CH, HI CH(CH3)2
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
Please answer all three if possible but mainly number 5
Br SCHLECH, 3. Assign R or Sconfiguration to the following molecules: Br F H. I H Br CH F F I . CH2CH3 CH2CH3 CH3CH -CH3 OH CH=CH2 H3C Сн, H "CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers c. identical d. Meso Compounds GH 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate...
Assign R, S configurations to each indicated chirality center in the molecules below. A. OH B. COOH НО. ---H co CHANH CH; HAN HO H norepinephrine alaine 0 D. C. H E. HOC OH moje H н. CH3 H2C H НО CO H CH2 tartaric acid dihydrocaryone
3. Assign R or S configuration on all chirial centers in each of the given Fischer projections. Then, draw the perspective drawing for each structure in the boxes below. Take particular care to indicate stereochemistry properly. 0 он HO- OCH HECH2CH2C HC Br HO H- I W OH H- a) CH₂ 6 CH₂OH OCH d) CH3 Perspective drawings:
3. Assign R or S configuration on all chirial centers in each of the given Fischer projections. Then, draw the perspective drawing for each structure in the boxes below. Take particular care to indicate stereochemistry properly. 0 он HO- OCH HECH2CH2C HC Br HO H- I W OH H- a) CH₂ 6 CH₂OH OCH d) CH3 Perspective drawings: