Please draw detailed step by step mechansim with arrows
Please draw detailed step by step mechansim with arrows OH 1) H 2) CH CH-CH Br,...
1. NaOEt CO2Et 2. H30+ 3. heat Br. Br CORET + H3C V CO2H H₂C + CO2 + E H3C CO2Et The malonic ester synthesis is a carbonyl alkylation reaction. It is used to prepare carboxylic acids from primary alkyl halides, lengthening the carbon In progress by two atoms. Thus, the product can be visualized as being a "substituted acetic acid." The reaction consists of three steps: generation of the enolate anion followed by SN 2 reaction with a primary...
Draw the arrows for the 7-step mechanism in formation of the mixed acetal shown. Map CH,OH OH mi # + HO ht Mixed ACETAL HEMIACETAL click to edit H. 0 Step он H Step w HỘ One H Two HⓇ H H 16 Step 3. Step HÖCH3 Step + H H Five Four Step 6 Draw the arrows for the 7-step mechanism for hydrolysis of an acetal to a carbonyl. Map . H2O Hö: H,O L; E i + CH,CH,OH...
Hi I need help predicting the products for these
reactions
OEt NaOCH.CH CH,CH OH b. H, O/H,0 a. NaOCH.CH CH,CH,OH b. Br c. NaOHH O, beat d. H2O*/H2O 1. NaCN, DMSO 2. CH,MgBr, Eto 3. H.O/H,O EN 2. NaH, CH,Br chemoselective 1. a. NaOet, EtOH Br b. 2. a. NaOH/H,O, heat b. H30+/H20 CY.NECEN cy OH b. then add HC-NH2 a. NaCN, DMSO b. HO*/H,0
Can you please show ( step by step with arrows )the
mechanism for how each reaction came about with its product. Thank
you
1. Br, hv 2. NaOCH, CH,OH 1. BrMgCH2CH3 CH3CH2OCH2CH3 2. dilute HCI. H20 110 DIASTEREAMERS 1. NaBH, CH,OH 2. HCI, H20 Br 141 HBr (excess) NaOC(CH3), HOC(CH3)3
1) + NaOH J) PCC OH CHCI K) H CH OH L) 1. Mg, ether Br 2. 3. H2O M) OH I Na Cr2O7 H2SO4
8. Draw a detailed arrow pushing mechanism for the following transformation. You must show arrows for every step, writing statements like “proton transfer” without showing the arrows for that step is not an acceptable answer. 1. NaOEt, EtOH لا ملہ ان ام Et 2. Hz0+, Heat
Which step is incorrect in the following reaction! Dicho Do in Do D20+ in D20 CHO 020- А в None are incorrect (all are correct) OB Ос Which intermediate is involved in this base-promoted hydrolysis? NaOH/H2O OH + OCH OKOCH, 1 olo options Which sequence of reagents would accomplish this transformation? 1. NaOEt 2. (CH3),CHCH,BE 3. H,09, Heat 1. NaOEt 1. NaoEt 2. CH,CH,CH,CH,Br 2. (CH),CHCH,CH,Br 3. H30*, Heat 3. H,0*, Heat 1. NaOEt 2. (CH3),CHCH, CH,CH,Br 3. H30*, Heat...
1) + NaOH J) OH PCC CH,C1, K) H СН,ОН L) 1. Mg, ether -Br o 2. 3. H,0 M) OH Na Cr 0 H2SO4 4. Propose Mechanism (Show your work) (14 pts) A) CH,CH,CH,OH CHỊCH CHỊCHCHỊCOH
COLUMNA 0 NO2 19 COLUMN B O + OH OH A) HAN AICI: 1) ch 2 BHA 3) H,09 B) YN B 1) My C) ОН 2) 2)CO2 3) H30 4) CH3OH D) 3) E) 0 OH H 1)DBAL-H 2)Ph PCH2 3) mCPBA 1) SOCI2 2CH.NH. pyridine 3) excess LAHA 4)H,0* F) 0 O 4) OH o G) excess HB H) 5) 1) 6) H30* Δ. Mglk J) 7) OH 0 2 1,0 hp question completion Status: Н. 6) Н...
19 1) mCPBA 2) MeOH,H 20 1) LIATH (excess) 2) H20+, H30+ 21 1) NaNH, 2) CH,CH,Br 3) HBr (2 equiv.) 22.Draw DETAILED arrow.pushing mechanisms for the following transformations: (8 points) H-Br: ër: