Question 4 Please predict the products for each of the following reactions: Na 1. Na 2. PrBr TsCl Py (pyridine) 1. TsCl, Py 2. NaBr, DMSO 9 10 SOCI₂, Py H-N→ CrO3Cl PCC OH Na2Cr2O7 H2SO4 5 HCI ZnCl2 2. KI, DMF 1. MsCI, Et₂N (base) A B C A C (BUD NO REACTION D
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- 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 REACTIONQuestion 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 REACTIONPlease predict the products for each of the following reactions: A Na 2. PrBr 1. Na 1. TsCI, Py 2. NaBr, DMSO SOCI₂, Py B 9 8 10 H-NO CrO₂Cl TSCI Py (pyridine) OH 3 1. MSCI, Et3N (base) 2. KI, DMF C PCC NO REACTION Na₂Cr₂O7 H₂SO4 HCI ZnCl₂ D OH
- 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 BrQuestion 3 Please predict the products for each of the following reactions: Na 1. Na 2. PrBr 1. TsCl, Py 2. NaBr, DMSO SOCI₂, Py 9 10 H-NO Cro₂Cl TsCl Py (pyridine) 3 OH 5 PCC Na2Cr2O7 H2SO4 HCI ZnCl2 1. MsCI, Et N (base) 2. KI, DMF A B с D ABCD H OH NO REACTIONPlease predict the products for each of the following reactions: Na A 2. PrBr 1. Na 1. TsCI, Py 2. NaBr, DMSO SOCI2, Py 6 8 Co 10 H-NⒸ CrO₂Cl B TSCI Py (pyridine) 6 2 OH LC 5 2. KI, DMF 1. MSCI, Et3N (base) с PCC H Na₂Cr₂O7 H₂SO4 HCI ZnCl₂ D OH
- Chemist Escoja los reactivos necesarios para la siguiente síntesis: A Br OH A = Mg, THF B = PCC, CH2C12 C= 1. acetona; 2. H2O Leyenda de reactivos: acetona = O + x + x formaldehido= H H MgBr B OH acetaldehído= HWhat is the major organic product of the following reaction? Problem viewing the image, Click Here O A OB O C OD A. B. C. C. D. 1. Hg(OAc)2, H₂O 2. NaBH4 D. OH t to allo OH OH f OH (+) OH (+) (±)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
- 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 OHQuestion 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 REACTION2. Predict the structure of the products (A-E) of the following reactions. BugSnH OMe AIBN Toluene, 80 "C OH 1) NaH, CS,, BnBr Ph B HO" 2) BuzSnH, AIBN H Toluene, 80 °C BuşSnH SPh AIBN Toluene, 80 "c 1) LDA, THF, -78 °C then PhSeBr D 2) H202 1) AIBN, SnBu, Me. Br E 2) O, then PPhg