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predict the products which would be expected. if multiple stereoisomers are possible draw all of them....
predict the product(s) which would be expected. if multiple stereoisomers are possible draw all of them. Br Br Br Br 1) xs NaNH2 2 H₂O Br
3.) Predict the products of each of the following and show all possible products and stereoisomers. Specify which product is the major product and which is minor. Identify which stereoisomer is favored or write racemic. HBE HBr H30* (cat)/H,0
Predict the elimination products for the following reaction. Identify the major and minor stereoisomers and draw them in the indicated box. This is a possible product, but the two phenyl rings repulse sterically, making this unstable. Consider the other more stable stereoisomer.
4. Predict the possible organic product(s) from the following reactions. Where relevant, show all stereoisomers. Pay particular attention to any information given in the product boxes. explair wnswers daw aroustolz OH Can you + HCI substitution AND elimination products + Н,о но., HCI only products with formula C1ghH1C +H2O H2SO4 OH only products with formula CeH120 HBr + 6 mono-addition products including stereoisomers 1 1
Extra credit: Draw all the possible products, including stereoisomers, for this reaca Br кон
Draw and name all possible stereoisomers of products of Wittig reaction between trans-cinnamaldehyde and benzyltriphenylphosphorous ylide. Which stereoisomer should be the most stable and why?
3. (16 points) For the following cyclohexane stereoisomers, draw all possible chair representations and rank them from lowest to highest in energy.
If appropriate, please include multiple stereoisomers with the appropriate dashes and wedges. Thanks! Predict the major organic product for the following multistep sequence. Be sure your answer accounts for stereochemistry and regiochemistry, where appropriate. If multiple stereoisomers are formed, be sure to draw all products using appropriate wedges and dashes. Ha CH3 1. H C 2. H30+ Нас CH3 Ph CH3 3. Ph
3. Draw all the products, including all stereoisomers that form when the optically active compound below reacts with HCl. Which of these will be optically active? Mengh HCI optically active
in question 3, are they asking for the stereoisomers ? which would be six possible stereoisomers ? If so then no need to answer question 3. Thanks. sorry, i meant question 2. 2. Draw all possible isomers of the following compound and assign all of the hydrogen atoms on each carbon atopm (except for methyl hydrogens) as homotopic, enantiotopic or distereotopic. 3. Estimate the ky/kp values for the following reactions and explain your reasoning. what can you be HCN H...