Question 7Please predict the products for each of the following reactions:ABCD1. Na2. PrBrNa101. TsCI, Py2. NaBr, DMSOASOCI₂, PyTsClPy (pyridine)H-N→CrO3ClBPCCOHNa2Cr2O7H₂SO4HCIZnCl22. KI, DMF1. MsCI, Et₂N (base)сDox o

Step 1:Step 2:Hence option B is correctStep 3: Step 4:

Answered: Question 7 Please predict the products…

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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Question 8 Please predict the products for each of the following reactions: ABCD A 1. Na 2. PrBr Na 10 1. TsCI, Py 2. NaBr, DMSO SOCI₂, Py H-NG Cro₂Cl Py (pyridine) OH PCC Na2Cr2O7 H2SO4 HCI ZnCl2 1. MsCI, Et N (base) 2. KI, DMF B с D Br
Question 5 Please predict the products for each of the following reactions: 1. Na 2. PrBr Na 10 1. TsCl, Py 2. NaBr, DMSO SOCI₂, Py H-NO CrO3Cl TsCl y (pyridine) Py ( PCC OH Na2Cr2O7 H2SO4 HCI ZnCl2 2. KI, DMF 1. MsCI, Et3N (base) A B C D А ABCD OMS NO REACTION
0 The target diol is synthesized in one step from 1-methylcyclopentene, but your lab partner exhausted the supply of that alkene. Fortunately, you have plenty of isomers (CH₁) on hand from which to synthesize 1-methylcyclopentene and, ultimately, the diol. Provide the missing reagents and organic structures needed to most efficiently produce the target product. reagent 1 Compound A Draw compound A. Select Draw Rings More с H Compound B Erase reagent 2 Identify reagent 1. reagent 3 H3C.. HO ....|H OH
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Question 4 Please predict the products for each of the following reactions: 1. Na 2. PrBr Na 10 1. TsCl, Py 2. NaBr, DMSO SOCI₂, Py H-N→ Θ Cro₂Cl TsCl Py (pyridine) OH PCC Na2Cr2O7 H2SO4 HCI ZnCl2 1. MsCI, Et N (base) 2. KI, DMF A B с ABCD NO REACTION D
Question 2 Please predict the products for each of the following reactions: 1. Na 2. PrBr Na 10 1. TsCl, Py 2. NaBr, DMSO SOCI₂, Py H-N→ Cro₂Cl Py (pyridine) OH PCC Na2Cr2O7 H2SO4 HCI ZnCl2 1. MsCI, Et N (base) 2. KI, DMF A B с D ABCD Н OH NO REACTION
HO NH2 CO₂Me PG! A NH HO PG² HO CO₂Me PG! NH `PG³ PG! `NH PG3 PG! `NH B PG2 CO₂Me C PG20 LiBH4 strong reducing agent, strong nucleophile PG! NH OH
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Predict the products, if any, of the following reactions. 20-35 (a) ascorbic ac (1) LiAlH4 -COOH (2) H3O+ (b) (1) NaCN CH₂Br (2) H3O+, heat (c) (1) SOCl2 (d) KMnO4, H₂O oct-4-yne (warm, concd.) (2) AlCl3 COOH (e) CH₂OH Na2Cr2O7, H2SO4 (f) Ph (1) BH3.THF CH3CH2-CH-COOH (2) H₁₂O+
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Question 9 Please predict the products for each of the following reactions: A ABCD 1. Na 2. PrBr เวรเ Py (pyridine) Na 10 9 OH 18 1. TsCI, Py 2. NaBr, DMSO SOCI₂, Py H-N'+ CrO3Cl PCC Na2Cr2O7 H2SO4 HCI ZnCl2 2. KI, DMF 1. MsCI, Et N (base) B с D Na NO REACTION

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Question 7 Please predict the products for each of the following reactions: ABCD 1. Na 2. PrBr Na 10 1. TsCI, Py 2. NaBr, DMSO A SOCI₂, Py TsCl Py (pyridine) H-N→ CrO3Cl B PCC OH Na2Cr2O7 H₂SO4 HCI ZnCl2 2. KI, DMF 1. MsCI, Et₂N (base) с D ox o