2a-m. Provide the missing product(s), reactant(s), or reagents for the following reactions. Show stereochemistry where applicable (including the formation of enantiomers or other stereoisomers). Note: this section continues onto the next page ( D G 1) CH3MgBr 2) H₂O KMnO4 concentrated A TsCl pyridine H₂ II H₂C-C-C-H H₂C-C=C-H H 1) LIAIH, 2) H3O+ B H₂C-C=C-CH3 1) Hg(OAc)2, H₂O H 2) NaBH₁ H₂C H CH3 F

2a-m. Provide the missing product(s), reactant(s), or reagents for the following reactions. Show stereochemistry where applicable (including the formation of enantiomers or other stereoisomers). Note: this section continues onto the next page ( D G 1) CH3MgBr 2) H₂O KMnO4 concentrated A TsCl pyridine H₂ II H₂C-C-C-H H₂C-C=C-H H 1) LIAIH, 2) H3O+ B H₂C-C=C-CH3 1) Hg(OAc)2, H₂O H 2) NaBH₁ H₂C H CH3 F

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...

See similar textbooks

Similar questions

ch Complete the following reactions by providing the missing products and reagents A-G. i) ii) iii) OH H₂PO4 heat Attach File O C E 2 0 N m-CPBA 1. LDA 2. HBr Pravics Local Cilac Br A ♫ D F 99+ a 1. Mg 2. O 3. H₂O+ B G N
9. Write structural formulas for the major organic product(s) for the following reactions. Be sure to indicate stereochemistry when relevant. (CH;CH,CH,),CuLi (a) Cl Br PAL2 (b) HO (c) CH;CH,CH,CH,OH C,H5MgBr 10. Propose a reasonable mechanism for the following reaction Be sure to include all intermediates. (transition states are not necessary) Br Br hv CH3-CH=C(CH3)2 + Br, ČH,-CH=C(CH3)2 CH2=CH–Ċ(CH3)2 11. Indicate how each of the following compounds could be prepared using the given starting material CH;CH,CH,CH3 CH;CH,CH,CH,Br CH;CH,CH,CH3 H,C=CH-CH=CH2 Br CH;CHCH,CH3 CH;CH=CCH,CH3 CH3
1. Predicting Products: Draw the structures of the major organic products of the reaction in the boxes provided. Stereochemistry should be shown if applicable. Each box should have a different molecule. 1) xs MeMgBr 2) H3O+ +
2. Predict the products of the following reactions, paying careful attention to which FG would react in each situation. Br Br OH OH 1) TsCl, pyridine 2) 1 equiv NaCN MeOH mod. heat Br Br OH OH 2 equiv NaOEt 1) PBr3 2) Nal in DMF
3. Predict the product(s) of the following reactions: CH3 CH3CHCH2CH2CO2CH3 2. Hg0* (a) CO2CH2CH3 (b) 1. DIBAH 1. CH3CH2MgBr 2. H30" (c) .COCI CH NH2, ? (d) CO2H CH,OH, ? H2SO4 но CH,CO,COCH,, ? Рyridine (e) CH3 (1) 1. LIAIHA 2. H30 H2C=CHCHCH2CO2CH3 (g) .CONH2 (h) CO2H SOCI2 1. LIAIH, 2. Нао Br CH3 e2016 Cenag Leming
Predict the major product for the following reaction. a) I b) II III d) IV e) V 1 IV OH NH₂ || 1. excess CH31 2. Ag₂O, H₂O heat V N(CH3)2 NHCH3
6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HO
biackboard.gwu.edu/webapPps/assessment/feview/review.jsprattempld Select the major product of the reaction below. 1) TIPSCI, Et3N 2) Na 3) 03, then CH3SCH3 4) CH3CH2LI, then H30* 5) Bu4N* F', H2O CI Selected Answer: Он HO Answers: он он он OH OH OH он Select the major product of the reaction below. The answer is there, but please explain step by step.
2. Show structures for the products formed in the following reactions. Indicate the major products where applicable. Br + NH₂ H HO OH Li(tBuQ)3AIH3 MeOH 1. LiAlH4 2. H₂O* 1. LiAlH4 2. H₂O* KMnO4 NaOH, A EtOH, NaBH CN cat. HCI
2a) (2 ) Provide the reagents or products for the following reactions. Include ALL stereochemistry, where appropriate. i). ii) iii) Z-4-octene CHO 1) MCPBA/DCM 2) H₂O* NaOCH, CH,OH .CO.I heat ol NH₂ OH
Predict the major organic product for the following reaction sequence. Be sure your answer accounts for stereochemistry and regiochemistry, whe appropriate. If multiple stereoisomers are formed, be sure to draw all products using appropriate wedges and dashes. H₂C CH₂ 1. BH3, THF 2. H2O2, NaOH, H₂O 3. PB13 4. (CH3CH2CH2)2CuLi ?
Reagent 3 list; commas separate the choices benzylamine,cyclohexlbromide, cyclohexylamine NaBH3CN catalytic H+, h30, NaOH Reagent 4 list; CH3(Ch2)2MgBr, cyclohexylamine NaBH3CN catalytic H+, Na2 Cr2 O7 H2O H2SO4,cyclohexabromide reagent 5 list; cyclohexylamine NaBH3CN catalytic H+,CH3(Ch2)2MgBr, cyclohexabromide, benzylamine