Do the reactions below proceed in good yield from left to right as shown? as) он pyridine lby но CI + NH CI O0 e) он +H20 Do the reactions below proceed in good yield from left to right as shown...
Do the reactions below proceed in good yield from left to right as shown? a) V NH2 + CH30 ZI + CH3OH X + HCI + Na ci X NIE pyridine 0 L - 10" NH HO 1 equivalent Do the reactions below proceed in good yield from left to right as shown? svom te - НСІ Viano HO OH LOH - „Domo NaOH H2O mä Na HON ZI 1 equivalent yes + HCI + Na ci
Do the reactions below proceed in good yield from left to right as shown? pyridine 10 Cool 0 1 equivalent trace of HCI OH + HO 1 equivalent + HCI Submit Answer Retry Entire Group 9 more group attempts remaining
?Do the reactions below proceed in good yield from left to right as shown?
Do the reactions below proceed in good yield from left to right as shown? ... ethos NA NaOH H20 Na o HCO OH . SOCH SO2 + HCI m y - wody.com + H2N-CHE Submit Answer Try Another Version 1 item attempt remaining
[Review Topics) [References) Do the reactions below proceed in good yield from left to right as shown? nyt - una to those Submit Answer Retry Entire Group more group attempts remaining [Review Topics] [References Do the reactions below proceed in good yield from left to right as shown? HAN 1 equivalent Submit Answer Retry Entire Group 9 more group attempts remaining [Review Topical References Do the reactions below proceed in good yield from left to right as shown? a) NH2...
W ОН CI E F Give the proper series of reactions, using reagents from the table below, that will carry out the overall transformations shown. (Assume aqueous workup where needed.) 1. Brz/ uv light 2. SOCI2 / THE 3. Mg/Et20 4. Meli/hexane 5. CH3CH2 MgCl 6. PhMgBr 7. NaBH4 8. LIAIHA 9. BH3 / ox 10. POC13/pyridine / THE 11. CrO3/THE 12. PCC/ CH2Cl2 13. Ht / H20 14. ELOH/H 15. t-butoxide 16. OH/H20 17. NH3 18, CO2 19. acetic...
Help! 1. 1. LIAIH4 / dry ether он 2. aqueous H2S04 2. AICl3 Ci но dSN2 Nucleophilic substitutiong a = Electrophilic addition b E2 Elimination c SN1 Nucleophilic substitution f Carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn Electrophilic aromatic substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a -i for your answers. 2. Review Topics] 1. HCI reflux он +...
1. Predict the major product for the reactions shown below; pick any 5: HO xs CHal Ag20 NaOEt EtOH, Δ -H2O HO но он 0 он H2SO4 H20, A heat 1) PhMgBr 1) NaOH, Br2 2) 5% HCI 2)H3O+, Δ OEt 1) PPh3 3) KOtBu 2) O 1) NaOH on. Br 2) O o 1. Predict the major product for the reactions shown below; pick any 5: HO xs CHal Ag20 NaOEt EtOH, Δ -H2O HO но он 0 он...
PPUCTy 627 All the following good yield. In som encountered. Neve lowing reactions have been described in the chemical literature and proceed in ald In some cases the reactants are more complicated than those we have so far ned. Nevertheless, on the basis of what you have already learned, you should be able to predict the principal product in each case. (a) NaC=CH + c Br B. (b) Br Br Y 1. excess NaNH, NH, 2. H0 BE on fa...
Which of the following sequences of reactions (from those shown below) would yield the desired product from the indicated starting material? 1- HBr. CC 2 HBr, ROOR 18 TsCL pyridine 19 NaOEt 20·H/Lindars Catalyst 21 NaNH, (0 22 Brg, hw 8 CH,CHCH CH CI 10- 18-crown-&, KF 25- 0s0, (catalytc), NMO 2) H-O2. NaOH 2) H' (aq) 2) H20 2) DMS 2) NaSH 2) NaBH 2)0% NaOH 2) H,0 12-1) RCOyH 27-1) HglOAc EIOH 14 “ to, 29 1)0 15-...