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
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- 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 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 OHQuestion 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 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 REACTIONChemist 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= HQuestion 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
- 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 D0 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 OH15. Did the reaction occur by SN1, SN2, E1, E2, or none of the above? Br F a) SN1 b) SN2 c) El d) E2 e) none of the above OHY A I need someone to explain why the answer is A please.
- 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 REACTIONH14.41 - Level 3 :: Unanswered • 3 attempts left Compound A produces compound E in four steps. What is compound A? a b C C D d E e Br 1) MeMgBr H2Cr207 1) MgBr H2SO4 (conc.) 2) H20 2) H2O NaBr Possible starting materials HO H. HO. a) b) c) d) e) AWhat 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 (+) (±)