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- Which of the given reactions would form meso product? H₂O, H2SO4 III m CH3 CH₂ONa CH3OH || H₂O, H2SO4 CH3 1. LiAlH4, THF 2. H₂O CH3 IVDraw the final organic product of the following three-step reaction of bromomethylbenzene. Br 1. NaCN 2. CH3MgBr 3. H3O*, H₂O Select Draw / ||| ||| Templates с H More N Erase Q2 QThe reaction shown can give two different mono-alkylation products depending on the conditions. Draw the kinetic and thermodynamic products of the reaction. 1. base Kinetic + Thermodynamic Products 2. CH3CH₂Br (1 equiv.) Draw the kinetic product. Draw the thermodynamic product. Select Draw Rings More Erase Select Draw Rings More Erase / ||| ||| C H O / || III C H O
- Choose the reagent(s) that would be most likely to complete this reaction. I||| / A B C D 1. BH3-THF 2. H2O2, NaOH Br₂ H₂O OsO4 (catalytic) NMO RCO3H Done4. Draw the final major product(s) for each multistep synthesis reaction. H3O* OMe H3PO4 Jones Et,NH reagent H30* PBR3 KOC(CH3)3 1. O3 NABH3CN HO- 2. DMS NH3, H3O* Br KOC(CH3)3 1. ВНз PCC H3O* 2. H2О2, ОН CH2CI2please explain why the circled answer choice is correct.
- 2. Propose electron-pushing arrows for each step of the radical mechanism shown below. PhO,s.-so,Ph jor for > H [w-o [w-o Pho2s-sO,Ph H5. Show the products for the following reaction based on the curved arrows showing the mechanism. CH3-O + Br H-CH₂-CH-C || HC. CH CH CH | CHDetermine the mechanism of nucleophilic substitution of each reaction and draw the products, including stereochemistr CH₂CH3 CI Br + CN d. + CH3COOH a. acetone + -OCH3 e. DMF f. b. C. ||||| a ||||| Br H Br CH2CH2CH3 + CH3OH DMSO H CH3 CI Br + OCH₂CH3 + CH3CH₂OH
- Draw the alkyl bromide for reaction 2. Select Draw Rings More Erase | 7 | | H Br Reagents Carboxylic Acid Product 1. Diethyl malonate, NaOC2H5, C2H5OH 2. NaOH, H2O 3. H3O*, heat ОН Draw the alkyl bromide for reaction 3.From the following reaction are step 1 and 2 correct?, explain why or why not and draw the whole mechanismCH3 || CH3CHCI CH3CH2CHCH,OH ČH3 a. Draw the structure of the tetrahedral intermediate INITIALLY FORMED in the reaction shown. • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na", I', in your answer. • In cases where there is more than one answer, just draw one. opy aste Previous
