Draw the product, pleaseกDL. CH,CH,CH,Mg Br2. H₂O1. H₂O*2. PCCJ. CH,MgBr4. HOLHCN KEN2. H,O A

We ahve to predict the products.

Answered: Draw the product, please ง ง L.…

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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HO ОН Cro H,SO, `CH3 f) H3C .00 Br2 -OCH3 FeBr3 g) CH3 NBS Na*O-t-Bu h)
CH3 HBr a) ? Br NaOC2H5 / isi b) 1.NABH4 2. Hао co,C2H5 1. Hg(OAc)2/THF/H2O d) 2. NaBHaГОн .CO2C2H5 isi e)
Cl Br h. -CH3 Br T H₂C-CH i. CH Cl CH₂CH3
OH Br₂ H₂C-H₂C CH₂. Br
Given the product/s of reaction, provide the reactants a. Н-С—С—Н b. -CH;Br + HBr С. CH,CH, Br
Select the missing reagents in the following multistep synthesis. Ignore any inorganic byproducts formed. 'H Š H O H₂O OH @ 1. NaOH, heat 2. Neutralizing work-up 1 H3O+ O TSOH, H₂O O H a A B C D E HOCH2CH2CH₂OH NaOH HOCH2CH2CH₂OH TSOH HOCH2CH2CH₂OH H₂O TSOH, H₂O CH₂OH(2 eq) TSOH
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.
Complete the following reactions My HC-O H&C KCN C. CHO Na HC-CH,-B d. H.C KMnO H.C HO CH KMrO, 0- + H,C~ H.C HI CH
CI ..*|||| Me CI Br H Br NaOH Acetone CH₂S: DMSO DMF MeOH ONa
What is the product? CALA © B. C OC. D OD. B MeO₂C A. CO₂Me H MeO₂C. ಚಿಕ C. MeO₂C B. MeO₂C. D.
Gu: For pair of structures below, tell whether they represent the same structure! b. CH3 a, CH3 AD OH Br CH3 OH H CH3 HO Br
Reagents a. CeHsCHO b. NaOH, ethanol c. Pyrrolidine, cat. H* d. H2C=CHCN e. H30* f. LDA g. ELOC(=0)CO,Et h. BRCH2CH=CH2 Na* OEt, ethanol j. Br2, H* k. K* t-BuO 1. CH2(CO2Et)2 m. heat Select reagents from the table to synthesize this compound from cyclopentanone. Enter the letters of the chosen reagents, in the order that you wish to use them, without spaces or punctuation (i.e. geda). Submit Answer Try Another Version 1 Item attempt remaining

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Draw the product, please ง ง L. CR,CH-CH-Mg Dr 2. H₂O 1. HO 2. PCC J. CH,MgBr 4. H,O LHCN KCN 2. H,O. A