PLEASE ADD CHIRALITY (R/S) AND STEREOSIOMER/RELATIONSHIP
mCPBA is an epoxidation reagent
Ring opening of unsymmetrical epoxide in acidic medium occurs at more substituted side while in basic medium occurs at least substitited side
Ether synthesis is SN2 reaction.
PLEASE ADD CHIRALITY (R/S) AND STEREOSIOMER/RELATIONSHIP What are the products or product produced in each reaction...
Starting from (R)-3-methylhex-1-yne as the substrate at the center of your page, draw a reaction map showing the regiochemical and stereochemical outcome or outcomes for each of the following series of reagents. Name each of your products, including stereochemical designations for any chirality centers that are generated.A. HgSO4, H2SO4, H2OB. 1. 9-BBN; 2. H2O2, NaOHC. Br2, CCl4D. HBrE. xs HBrF. HBr, ROORG. xs HBr, ROORH. 1. O3; 2. H2OI. H2, Lindlar's catalystJ. Na, NH3
1. What substitution mechanism will the following reaction likely proceed through? (1pt) CH3 HU. : N=C: +3C-Br - NC-C WH + Br HT 2. Label the componetns of the above reation as: Nucleophile, electrophile, leaving group (3pt) 3. Assign R and S configuration to the following reactant and products (2pt) NaOH HO + HO-COCH3 H.COwc-OH + HO-6 H2COCCI H H 4. What ratio should the two above products be formed in and what is their stereochemical relationship? (2pt) 5. Predict...
What is the general class of each test reaction in the introduction? Precipitation? Acid-Base? Oxidation eduction? anoina to aizy ona svidstils Reaction Class 1 2 iliw 15 TO15192do art sshommua bns nosgol rond dass 101 12575 gbubnium oY noi de lo enor Som 10 910 w II woy Xd on abian aningstid on naloga uzib 3 OOH 4 5 DHET 6 7 SET adus 00 9 Complex ion formation 10 11 No reaction 12 13 14 Combination 15 16 17...