We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
Draw the products formed in the reactions below: 1) LDA 2) 3) H20 NaOCH3 b CH3OH,...
2) CHs LDA 1) LDA 3 2) Ci OH, H20 -OH, H2O CHO 1 LDA 2) CH3CH2Br Он, H2O 1) NaOEt 8 2) NaOEt OEt 10 Cl NaH 2 (excess) 12 HO Bra(excess) 13 HO LDA 14L THF, -78 C NaOEt, EtOH NaOEt, EtOH 16 NaOEt, EtOH 17 Br но 18 OOEt 1)NaOEt, EtOH 2) H3O 19 OEt 20 l HO o CHO + H20
colecta NaOH H + CH3 then heat NaOH tir then heat NaOH (CH3)2Culi then heat 1. NaOCH3 CH3OH OCH3 2. dil. HCI O 1. LDA 1. LIAIHA het hy 2. Br 2. H2O* 1. NaOCH3 1. NaOCH3 2. CI OCH; 2. Ph Br 3. H3O+, heat 1. LDA 1. LDA 요 2. 0 CI 3. H3O+ 2. H 3. H30+
Provide the products for the following reactions:
1. LDA, THF, -78 C 1. LDA, THF, -78 C a yoyo a la misma 0 2. VI NaOCH3, CH3OH 1 eq. 2. H30*. H20
1. Draw the product(s) of the following reactions. Include stereochemistry when relevant. If stereoisomers are formed then draw out and label the relationship between your structures. Ph-N3 40°C HN-NH2 SACOMe 150 °C d. CO2CH3 210 °C нсОСН3 In hv ZI 160 °C OBn 85 °C OBn OBno= o 1 equiv. CI K2CO3 heat PhCH N= H 1. LDA (1 equiv.) P 2. Ph Ph 3. aqueous work-up heat EtOH NaOEt 2. Draw the mechanism for the following transformations. I Н...
1. Predict the major organic products of the following reactions. Draw all stereoisomers that are formed. НО, OH 1 eq ,H2SO4 (assume H2O workup of reaction to neutralize product) 1. LDA 2. (assume H,O workup of reaction to neutralize product) 3. Hg(OAC)2 4. NaBH, EtOH 1eq HBr EtOH ambiente 1. Brz. CCL 2. NaOET, ETOH OH
Please write neatly.
3. Show the products formed in the tollowing reactions draw two enols 1) Mg. Et O 2) CO2 3) H:O NHz Jo .OTo. 쁘. pyridne CI NH Ci CI 0 SOCl OH heat NH 1) CH3MgBr excess CH, CH, -OCH,C 2) H2O COOMe LIAIH OH Ci 0
3. Show the products formed in the tollowing reactions draw two enols 1) Mg. Et O 2) CO2 3) H:O NHz Jo .OTo. 쁘. pyridne CI NH Ci CI
0...
Question 4 (4 points) What is the final, major product of the synthesis below? CH3OH 1) O3, CH2Cl2, -78 °C 2) H202 NaOCH HOCH ?. H2SO4 (cat.) CH3 Question 5 (4 points) Predict the product(s) of the following Diels-Alder reaction below. - ? COOCH3 + enantiomer COOCH3 N NCOOCH COOCH N-COOCH N-COOCH, Question 6 (4 points) What is the correct set of reagents for the synthesis of the compound at right with the starting diene at left? H₂N. NH2 H...
draw or name structures in 1-3. in the reactions, draw the
products or write the reagents
Naming: 2) 5 - hydroxy-6-methyl-3,7-dioxo - 5-heptenoic acid DO 3) oH ich Y Reaction : 1) Mor - 1) | -| 1. Mg CI 2. CD 3. NH, C,H, 0. 1.H, OH 2. Br₂ , H₂O 3. PDC 1. MAI 2. H30+ 3. Ts CI 4. LDA
Predict the products for each reaction shown below N NaOH N NaOH THF LDA 1) NaH, THF EtO THF-78 °C 2) CH3CH2Br heat HO CH3COOH KOH CH3NH2 KOH MeOH 1) NaOMe, MeOH 1) HCI, H20 OH 2) PhCH2Br 2) 180 °C
Q1- Fill in the boxes with the product of the following reactions. Draw only the PREDOMİNANT REGIOISOMER. When a racemic mixture is formed mark the chiral center with an ASTERICK () and write RACEMİC in the box. 1 Eq LDA 0 1 Eq NaOH 1) 0.5 Eq LDA1) Cat NaOH 2) H30 јнзо-, Heat , NaOEt, EtOH 1. NaOEt EtOH Br 1) NaOH, H2O 2) H3O 3) Heat 1) (CH3)zMgBr 2) H30 2 a2- Fill in the boxes with the...