draw all products circle the major product if there are only I product or no products are preferred don't circle if rxn produces 2 stereoisomers draw both and if it produces multiple regioisomers draw all of them and circle single most stable 3 кову
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- draw all products circle the major product if there are only I product or no products are preferred don't circle if rxn produces 2 stereoisomers draw both and if it produces multiple regioisomers draw all of them and circle single most stable I Na MeA B Br FeBr3 1 2 0 =Li then H30* LIAIH4 then H3O* Propose reaction conditions (A) and draw the products (B, C and D) of each transformation. Curved arrow mechanisms are not required.S) Draw the expected major product (except when I explicitly ask for a minor product) in each box NaOCI CH;CO,H : CH,CN : H20 1) `MgBr OH 2) H20 C10H180 C12H240 C12H240 major stereoisomer minor stereoisomer base C13H9F203 "Fiflunisal" NSAID Drug produced by Merck in 1971 NC. CN heat C10H12N2 enant #1 C1OH12N2 enant #2 show "relative stereochemistry" of the methyl groups in the product for full credit. Two enantiomers are produced, draw one in one box, the other in the other box.
- Label each stereogenic center as R or S. R S НО. Br О CI Br ОН ОН4. Draw the products or reactants: ** a NC NC H3COOC- H3COOC include stereochemistry CN CN CO₂H O CO₂H Draw the endo/exo10:06 .l LTE chem1 CI CI Compaund A Compaund B a) draw the enantiomers of Compound A and Compound B if possible b) what is the Structeural reationship between compaund A and campaund B? ••. Share Modify Comment More
- Ⓒs Draw the specified TMO for each of the given Spueres. I nodes are there Ⓒ HOMO of N (ally cation) ] How many о номо @ Lumo of Dr (allylanion) in each of the TMO drawn ⒸHOMO of 1,3- butadiene Ⓒ LUMO of etherer) CH3COH [H] CH3CH₂CH₂NCH₂CH₂CH3 CH₂CH₂CH3 ? [H] + CH3CH₂CH₂CI BASEo o HCI Br₂ Br₂ H₂O Addition Stereochemistry 00
- Draw the major product from this reaction. Use a dash and/or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore acid byproducts. mCPBA Q AtQ7. Using the CabolagaldRKalog rule, assign the absolute stereochemistry to each stereogenic centre in compounds a-d, and determine whether they are chiral or not. a) b) OH OH H3C CH3 H3C CH3 NH2 c) d) OH H -0 H- H3C CH3 н он OH ОНPredict the major isolated organic product. 1. NaNH2 2. CH3BR 3. H2, Lindlar 4. MCPBA OH А. С. OH OH D. ОН OH A. B.