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- Considering stereochemistry, draw the resulting E2 elimination product when H, is removed. H₂ H All H Br |||| X AJ U: S G9) Draw the conformer structure, Newman projection, before elimination and the elimination product of the following reaction: Br CH3ONA HONZ IS ON Determine which substitution mechanism occurs and draw the products, including stereochemistry. + -OCH3 DMSO Br H + CH3OH Br CH,CH, CH3
- For the following reaction, decide whether a solution of the products would be optically active or not and why. You will need to know the product of this reaction in order to solve this problem. To preview the image click here Br CH3 Na: CEN: acetone O Not optically active, achiral product is formed O Not optically active, racemic mixture is formed O Not optically active, a meso compound is formed O Optically active, a single enantiomer is formedPredict the stereochemical outcome of the following E2 reaction: CI CI4. Draw the products or reactants: ** a NC NC H3COOC- H3COOC include stereochemistry CN CN CO₂H O CO₂H Draw the endo/exo
- Draw a veasonable mechanism for this reaction that involves free radicals. hv DH cat. OH Ph Pn H,CUse mechanism arrows to show the mechanism indicated for each reaction. Draw all possible regiochemical and stereochemical products and indicate if the reaction solution is optically active or not. OTS Ph NaNH, SN2 CH₂OH SN1 Is the reaction solution optically active: yes or no?. Is the reaction solution optically active: yes or no?Select all the possible enols for the following compound? Colect Compound OH on of all es e u B G A F BOOOO
- Determine the major product(s) of the following reaction: (En: enantiomer) Bľ2 Br, ? H,O ОН A) + En Br Br В) + En Br ОН C) + En HQ Br YOH D) + EnDraw the favored product(s) of the following reactions (organic chemistry)What is the major elimination product obtained from the following reaction? CH3 CH3 NaOCH₂CH3 HOCH₂CH3 Ot-Bu || CH3 Ot-Bu ||| CH3 IV CH3