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5. Show the expected products for the following reactions: (2 pts each, 16 pts total) 0...
5,6,7,8th please 5. Show the expected products for the following reactions: (2 pts each, 16 pts total) 0 O NH 1) Conc, KMnO4, NaOH 2) H20+ 3) xs PhMgCI 4) H20" 1) KCN, HCl 2) PCC, CHCI 3) PhyP 1) dilute H2SO4 2) PCC, CH.CL 3) NH w 1) SOCI 2) EtMgBr 3) H.O ОН 1) KCN, HCl 2) H0 3) SOCI, 4) i 1) HCI | 2) HENNH. [H] 3) KOH,H,O, heat 1) RCO,H 2) LAIH 3) H.O 4)...
This is really important. If you are 100% sure it is corect then thank you. 5. Show the expected products for the following reactions: (2 pts each, 16 pts total) NH 1) Conc, KMnO4, NaOH 2) H,0 3) xs PhMgCI 4) H, 1) KN, HC| 2) PCC, CHCI 3) Php 1) dilute H2SO4 2) PCC, CH.CH 3) ΝΗ 1) SOCI 2) Mir 3) H0 ) KCN, | | 2) H0 3) SOCI: 4) 1) HCI 2) VIỆN NHẸ. [W] 3)...
Question 4: Complete each of the following reactions by giving the principal organic 20 pts product(s) COOK diazomethane А KOH PhCH BI COOH B b) 1. LAIH SOCI D соон E 2. H,0 1. NaBH LiAlH, F G d. 2. HBT 3, KCN sodium acetate e. CHỊCH CHÚCOCI H ру 1. LiAlH CH-CH-CH-CH-COCl + CHỊCH-CH-CH-NH, 2. H2O
1. Write structures for the lettered organic product(s) in the following reactions: (4 pts each) H, CH2OH A 1) CHCI B 2) OH OH O== + с D + E Conc. KMnO4 OH/H,0 OH PBrz F CH2CH MgBr CH3MgBr H H30 1) 03 2) Zn, H20 2Eq. HBT H3C-CEC-H NaH H3C-C=C-H K
For Questions 9-13, choose the correct reagents for the following functional group conversion. 9. A. PCC B. H2CrO C. NaBH.4 D. KMnO4 10. 2 HO CN A. HCN/H2SO4 B. KCN C. HCN/KCN D. NH:/NaOH 2 он A. 1) 4-bromobutanal /2) Mg'/ether /3) H B. NaOH MgBr D. LDA 12. CI Zn(Hg) HCI B. 2) Raney Ni, H2 1)H2N.NL 12. CI Zn(Hg) HCI ) 15 B. 2) Raney Ni, H2 1)H2N C. 2) NaOH/H20, heat NaCI D. 13. 2 Zn(Hg) HCI...
5. Give the organic products of each of the following multistep syntheses. You are required to draw only the structures of the final products. Drawing the products of individual steps is optional and may be graded for partial marks. No mechanisms are required. 1.H20* 2. Na2Cr207, H2SO44 2 a) 3. PhMgBr 4. H2O 1. EtMgBr 2. H2O 3. Na2Cr207, H2SO4 (aq) 3. EtMgBr 4. H20 1. NaNH, 2. Mel 3. NaNH2 HCECH 4. Eti 5. Na, NH, 1. Mg /...
The best way to synthesize the following amine is: HN 1. SOCI 2. ex NH; HO 3. LiAIH 4. H20 1. NaN; Br 2. H. Ni 1. NaCN Br 2. LAIH, 3 H,0 1. ex. NH 2 LAIH 3 но HO
2. (40 pts, 4 pts each) Prediet-the-products. Draw the major organic product after each series of reactions. You must draw the correct regioisomer and/or stereoisomer for full credit. Some schemes contain more than one step; you do not need to draw the product after each step. Only the final products drawn in the boxes provided will be graded. 1. Brz, CHCI 1. Na, NHI -CHE 2. NaOMe (xs) DMSO 2. mCPBA CHCI 3. H. HSO4 НО. CI Но, Me 1....
4. Synthesis Reactions. Draw the feature product of the following reactions. (8 x 3 pts) 1. Mg Ph Br 2. CO2 3. H a "NH2 Ph 1. NaOH, CI 2. LAIH b. CHỊCH NHA NaBHgCN, H+ Ph C. Br (excess) NH d NaOH H HO OH H CH e. 1. NaOH H2O NH 2. H+ o= 1. NaOH H2O 2. SOCI N(CH3)2 3 HO
NO, 00) 1.80.H.SO 2 онкона 3.HO pp.) 2 Na NDIO 1.2.2,0 2 DO XS PCC HO CH ON OH XSHCIO NH إياها NINH w.) OH OH XS Bobbitt's SiO, CH2Cl2 ww.) OH 1. XS KMnONaOH(aq). A 2. H,O* HO 1. NaNO.HCI 2. H,PO (a) CHO NH yy.) NH 1. NaNO, HCl(conc) 2. D.PO 1. LITHF 2. D20 14 aaa) wo NaBHJEICH bbb.) су Cl2 FeBry HO НО. Feb COL) H 1 KM. NOW 2. Ho didd) cleum com) NO 1....