Identify four electrophilic sites in the molecule below.69Aubagio(Teriflunomide)F3C.В`NHNC.`OHHA|C Identify the product of the following reaction:AOH1.MgBrEt,0 (solvent)జయ2. NH,CIAВCD

Four electrophilic sites are B C G F

Answered: 69 Aubagio (Teriflunomide) F3C. `NH NC.…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Predict the product
105. Determine the one or two steps it takes to get from the starting material to the product using the reactions found in this chapter. a. b. H₂C-C OH *-* OH H₂C-C H₂C H₂C U=O CH₂ CH₂-OH CH3-CH-CH₂-CH-CH3 I CH₂ - CH3 CH3–CH2–C-CH, CH3 O CH₂ || CH3-CH-CH₂-C-CH3 CH₂CH3 Br CH3 CH₂-C-CH3 CH3
O Reagents Available a. CH₂=CHCH₂CI, AICI 3 CH3 b. CH₂Br₂, OH™ C. CH3CH₂COCI, AICI 3 d. H₂, Pt e. NBS, CCI4 f. K* tBuO™ g. CO, HCI, CUCI/AICI3 h. CH3CH₂CH₂COCI, AICI 3 i. BrCH₂CH₂Br, OH- j. CH3CH₂CI, AICI 3 k. RCO3H I. H3O+ Using conditions from the table, show how you would synthesize this compound from catechol (1,2-benzenediol). Select reagents from the table in the order that you wish to use them, i.e. aced; do not include punctuation or spaces. If more than one route exists, choose the shorter one; in no case will a synthesis require more than 5 steps.
1. Fill in the missing products or reactants. OH lydle you diw pantera endio garis 1. CH3CH₂MgBr 2. H* SOCI₂ 10 OH 01 OH H3O+ 1. Na 2. CH₂Br OCH₂CH3 CH₂ N ₂
25 идё массам 1) Tsci 2) NaI S excess CH₂ MI Felly/Al₂O3 (ene reaction) CH₂D AIM CI (Prins Fan) E B COM X Naci DMSD 150°C how is this formed?
Predict the reagent(s) needed to perform the following reaction. O OH O
Complete the following reaction 165yb + 161 Er e 165 Er +Ve et n 165Tm 165 Lu 165Hf Р
29 eBook Print References What product results from this reaction? HC с HC A 2 c=c H3C H3C HO CH3 CH3 c=0 CH3 H3C H3C-c-c - CH3 I ОН CH3COOH B D Д H3C H3C - C — CH3 c - CH3 CH3 H3C H3c-c-c - CH3 | | H OH

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69 Aubagio (Teriflunomide) F3C. `NH NC. `OH H A |C E G