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- Predict the product(s) and provide the complete mechanism for each reaction below.Consider the cyclization reaction mechanism that is partially detailed below and predict the structures of key intermediates. Only draw resonance structures with carbanions and not oxyanions. G CH;00C [1] NaOCH3 [2] H2O COOCH3 Na* :OCH3 H H- CH;ö. :0: :0:e Give the mechanism for the following reachou. CHOH exass CHO OCH3 + H-O
- Q, - write a Mechanism that explains hint he stereochemisty (sed pmacal rearangemendy a) CotH6 fonn Hcl b) HeoH O wr,te he Mechanism fer OH CHBrg NAOH (Carbene)What will be the major product of the following reaction and what is the likely mechanism for its formation? (CH;);COK Br racemic OCCCH3)3 OCCH3)3 ÓCCCH3)3 A B C D EQ1. For each reaction, give the expected substitution product and predict whether the mechanism will be first order (Sy1) or second order (Sx2): a) 2-chloro-2-methylbutane + CH;COOH b) isobutyl bromide + NaOMe c) 1-iodo-1-methylcyclohexane + CH;CH;OH
- P CHE 124 ORGANIC CHEMISTRY TUT2 2020 (Prote on Failed) Mailings Review View n and might be unsafe. Click for more details. Enable Editing 2. What are the major products obtained from the following reactions? Indicate the geometry (cis/trans). HBr, CH,COOH 近 91 81 61 L. 5. 8. 6.Q2: Suggest mechanisms for the reactions belowe OH TSOH OH OH OH TSOH OHQ1 Complete the following reactions with mechanism ( OCH3 AICI, i) CH3-CH3-CH3-Ci NO2 dilute HNο, ii) CH3 iii)
- Give a complete mechanism with step by step in details OMSO I10'cPropose a complete mechanism to account for the two products of the reaction shown below. Please illustrate any and all intermediates, resonance forms, curved arrows, formal charges, and lone pairs as necessary. CI OCH2CH3 Br HCI Br + Br CH;CH2OH2. For each reaction, give the expected substitution product and predict whether the mechanism will be first order (Sw1) or second order (Sw2): a) 2-chloro-2-methylbutane + CH;COOH b) isobutyl bromide + NƏQME, c) 1-iodo-1-methylcyclohexane + CH;CH;OH