8. predict the major organic products of each of the following reaction conditions? 9. show how...
8. Predict the major organic products of each of the following reaction conditions (20 points) 1) LiAIH diethylether н 4 2) Н-о Н.о KOH CrO,, H,SO,, H,О он acetone (co-solvent) 1) CH3MgBr, diethylether 2) Н-о 9. Show how you could synthesize the targeted products from the starting epoxides. Show all reagents and reaction conditions in the boxes above the reaction arrows Но Hас ОСHЗ но O
Predict the major organic products of each of the following reaction conditions Н.О + КОН CrO3, H2SO4, H20 HO acetone (co-solvent) 1) CH3MgBr, diethylether 2) H2O
7. Predict the major organic product or provide reagents needed to complete each reaction. 1. CH3NH2 (a-b) excess 2. LIAIHA 3. H20 ia -NH ?? excess (c-d) HO NH2 triethylamine ? (e-f) CEN 1. CHẠMgBr 2. H20, H NH2 (g-h) H20, H* H2. Pd (1-1) CH3NH2 4 products (m) 1. LAIH 2. H2O, H & NH (n) 1. LiAIH4 2. H20, H+ 8. Predict the four possible Aldol condensation products and their dehydration products. KOH, H20.A + H 1. Predict...
Predict the major organic products of each reaction below. Show appropriate stereochemistry when relevant. 13. (30) Predict the major organic productís) of each reaction below. Show appropriate stereochemistry whern relevant Na, NH3
Predict the major organic product or products for each of the following. Be sure to include stereochemistry where appropriate. Assume each is in the most appropriate solvent. Remember, "no reaction" may be an answer. Please clearly label the answer and explain in detail. Thanks in advance. HgSO4 H2SO4 H2O Br2 HCI 0 MgBr - b) H+
HO HO 17. Predict the major organic products of each reaction. (8 pts.) 1) Hg(OAC) H2O 2) NaBH
a) Complete the curved arrow electron-pushing mechanism and predict the major organic product of the reaction when 1-chloropentane is treated with hydroxide in ethanol as shown below. Use curved arrows to show the conversion to the product. Draw the structure of the organic product formed in the reaction. Draw lone pairs. CH3 :ci: СНЫСн,он HO b) Select the option that describes the mechanism of the reaction above. 10 SNI OSN2 Ο Ε1 lo ez
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
1. (10 points) Predict the major organic product or products for each of the following. Be sure to include stereochemistry where appropriate. Assume each is in the most appropriate solvent. Remember, "no reaction" may be an answer. a) O3 b) DMS HgSO4 H2SO4 H20 B12 HCI MgBr b) H+
Predict the products of the following elimination reaction. Draw the major organic product formed in the following reaction. For the alcohol reaction below, give the major organic product.