Need help with the R and S configurations for the two chair questions numbered 1 and...
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers and meso compounds. II) Assign the absolute configuration of chiral carbons in each molecule OCH3 HO+Br HS+CN H2N-CH3 HOSH Он HO+CH3 н OCH3 Сн, ососна Br +D HOCH HC-BrHN+Br CH 8. For the following compounds, assign the absolute configuration for those with chiral carbons and identify those that are NOT enantiomers HO C-C-OHY -CCIN 13CH3 HAN CH3 CH3 осі H-CH3 H2N+CH H O+COOH...
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
please help!! Glycerol could react with an excess of which of the following to form a fat or an oil? Choose all that apply Cн,с-он CHsNCH2CH сн CH3(CH2)18COOH CH3 (CH),CH-CН СH)-СООН Cн,сн,он Which could react with an excess of the following to form a fat or an oil? он Choose all that apply req req OH Н он 2req но он 2req OH OH Previous
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
Need help with these ones. ОН СООН С Bг ОН СООН СООН Он сH-N СОO NHA* ОН ОН SOCI, (еxcess) он Н,о* (R) COOH А но СООН A/Н,0* о о- A) NH2 B) N1 Hint: Reductive Amination C) racemic D) Br со, ОН E) но F) КCN
I only need help with f, g, h, and i. Thank you! 2. Indicate if the following structures are chiral or achiral (remember to look for the internal plane of symmetry) a) (CH3)3CCH(CH3)2 b) CH3CH2CH(CH3)CH2CH3 HO OH Он d) он но. Сно CH3 i)H3C. g) h) Н- Br CH20H н н- -Br НООС С. Н CH2CH3 CH3 H н CI
having trouble with R and S configuration, can someone help out with this sheet? 17 Br>Cl'7 S"7 F>ONTO77i77 H 1. Determine the configuration (R or S) of each of the following molecules: (Ph phenyl, a benzene ring as a group) CH-CH3 b. CHs с. но NH2 d. он COOH Ph H Hас CH2CH3 H2N CH&CH NH2 NH2 f. Ph CH3 Ph CHs h. H i. OH c lCOOH н.сн,с F Н.с NH2 h. COOH CHs CH2CH H2N 2. Label the...
Hello just double checking my ochem study guide, please answer ALL the questions you see below, if not let someone else do them please! High rating only given to ALL questions complete Provide the relationship between the two structures shown. In the space provided, indicate S, if the two structures represent the same conformation of the same compound, CF, if the two structures represent different conformations of the same compound, CI, if the two structures are constitutional isomers, E, if...
5:43 PM Thu Oct 31 29% Chem2542 Assignment-6.doc 1. Provide the structure of diene and dienophile required for the synthesis of the following compound via Diels-Alder reaction. Ph сно сно 2. The following a,b-unsaturated ketone can react with nucleophilic reagents to yield 1,2-addition as well as 1,4-addition (conjugate addition) products depending on the nucleophilic reagent. Provide the structure of the major primary 1,2-addition or 1,4 addition product formed in each reaction 1. CH,MgCI 2. HC 1. LIAIH 2. HC 1....
3. Assign R or S configuration to the chirality centers of the following molecules. ҫн, сн, b) но н H Br COOH c) H CH COOH CH,CH н. сн,Cн он HO d) H Br H Br h) CH CH,о, g) HO Н СООН CH hway.com