Predict the product of this E2 elimination reaction. 1 ||| Br H3C Ph f Ph Ph H3C Ph Ph H CH3 Ph || reaction CH3 H3C NaOCH3 IV Ph H₂C Brill Ph CH3 Ph CH₂ Ph
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- Synthesis - Drawing Saved Synthesize the following compound from cyclohexanol, ethanol, and any other needed reagents. он Part 1 out of 2 plnts Preparation of organometallic reagent: еВook Print References A B CH3CH2OH CH3 CH2MGB. draw structure ... Draw the intermediate product above and select the correct reagent for A. O Br, O NaBr O HBr O Select the correct reagent for B. O Mg O MgBr2 O MgI, O MgO Hin Soluti raw 11 e here to searchWhich of the following substrates will have the fastest rate of reaction with NaCN in DMSO? OA) B) Br O D) CI3. Predict the major product for the reaction shown here and draw the complete detailed mechanism for each reaction. Explain your answers. Provide which product is the thermodynamic and kinetic product. O: e 1. LDA 2. CI CHE 1. NaOC(CH3)3 2. CI
- can you explain how can we determine major and minor product from these reaction elimination-addition? &=&=1561=6, NH₂ majo CH, NH₂ NH₂ &=-&-&-& majo CH3 OCH, CI NINH, NH 3liq. KNH₂ NH309. Br ΚΝΗ, NH CI CH₁ 80 80 OCH, majo NH, NH₂ mino CH3 mino NH₂ NH₂ NH, NH, CI majo CH3 majo NH₂ NH₂Determine 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 + CH3CH₂OHFor the following compound: ته HO Draw a mechanism for the tautomerization process under BASIC conditions: Mechanism A: H-5: ·H Mechanism B: H-5: -H Mechanism C: H-0: H-O: Mechanism D: . © H-OH2 ل سے -H م - H-O: H-OO که فری -H H-00 H... H ·H H H m-o-m H: H H H H... H ته + H-OO H-00 O. H :: H © H-O-H -H
- 10. Draw the complete, detailed mechanism (curved arrows) for the following reaction, and predict the major product. CH3 ▪OH 1. DMSO (COCI)2 2. Et3N H1. Provide the mechanism. shay=& NaOEt EtOH CO₂Etat product will result from the reaction shown? (Just mention the class of compound not the nomenclature) CH3 HOCH,CH,OH CH;CHCH,CH,CH,C-H H+