
Last part is not in English language .
CHINH, HN CHINH, 19LiAH 2) H,0 Br NaN, 1) LAH 2) H0 1) LAH 2) H.O...
Me Me Br Me MgBr 2. HaO H+ cat 1. NaN 2. LiAlH4 (LAH) then Haot Et 1. LDA, -78 oc then Me O. Et NH OH Ph
А NaOH Heated KOH Reagent Reapeut Product 1 Hgso/H.O H Br/h 144a HLV Pa at 2.H0 . LDA OH CI: Repeat 1.) Su BH Product 2 2.)H,O, NOH NBS/ 50% H,SO4 Н,0 ОН ОН ОН ОН т ОН A с D
1) Provide structures for A-J in the following roadmap. H NaN LiAIH SOCI, CHINH + B с D- CH,OH (xs) CH,OH E+ A CHOS 1) KOH, H20 2) H,07 NH SOCI 2) Propose a mechanism for the following transformation, including arrows to describe electron flow, and all intermediates. CN Oro NaOH H2O are OH
H,Cro SOCI: H,0 Pyridine PCC CH,CI, HIO HR Peroxide 2. H,0,HCI NES CH- - HN CH,I, Zn(Cu) ether 1.0, 2. (CH) KCN HCN 1.00 2. NaHSO, H,0 HO 2. HCI, H20 H.SO 1. BH. THE 2. H,O, NaOH 1. HgOAC), 2,0 2. NaBH, HUNCH, 1. NBH 2. H.O
2. Predict the product. CH,CHINH Or . 1. excess CH 1 2. Ag,0,H,O heat 5. Match the reagents to the corresponding reaction. G. H20 H. xs CH3CH2NH2 A. SOCI2, pyridine B. Ethanol, pyridine C. 1) xs LAH 2) H20 D. 1) xs CH,CHMgBr 2) H30 E. 1) NaOH 2) H30* F. 1) DIBAH 2) H20 1. 1) LiAl(OR)2) H20 J. (CH2CH2) Culi K. xs NH3 L. 1) NaOH 2) CHÚCHỊCHÚCOCI M. Butanol, H
7) OH 1. NaBH 2. H.O OH 8) NaOH HOO, A HT 9) Ph Ph El siguiente compuesto fue sintetizado en 2 pasos a partir de una cetona y el ión de 5) cianuro. Haz un análisis retrosintético para determinar la estructura de la cetona.. No es necesario escribir las condiciones de reacción. (3 pts) HO OH ión de cianuro cetona 1
The best way to synthesize the following amine is: HN 1. NBS, hy 2. NaNH, NHÀ 1. HNO3 H2SO4 2. Fe, HCI 3. NaOH 1. Biz, FeBrz 2. NaN; 3. H. Ni 1. NaCN Br 2. LiAlH 3. H20
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
pls do B to P thanks
HCFO AIC Br CH O A (Substitution) NO 1) LDA 2) H,о* 1) NaOh 2) 3) H5o', A 2) нCL H,о H then H.O EIMgBr H 1) Eto 2) но", А EtO OEt CN NaH J Br LDA/THF K -78 °C Br LDATHF L 0°C Br S H2 Raney Ni M 1) CF COOOH 2) LIAIH N Ph.PECHCH ETOH P HCI
HCFO AIC Br CH O A (Substitution) NO 1) LDA 2) H,о* 1)...
Pages 1. BH THE 2. H.O., NaOH Cly, H,0 r Chino 1. HP 2. Radiactive Works