

5. Indicate the preferred product for the following reactions. Assume proper work-up for each step. (7...
5. Synthesis Reactions: Draw the major products for the following reactions (need not show any byproducts). (3 points each, 21 points) Note: For Diels-Alder reactions, be sure to show relative stereochemistry, if appropriate. CH (be sure to specify the CN product stereochemistry) So, H2SO. b. Br OCH AICI, (show monosub, only) 1. AICI, 2. Zn(Hg), HCI 3. HNO, H,SO d. нс Bry FeBry OCH (be sure to specify the product stereochemistry) f. 1. Brą, hv 2. NaOH
1. Provide the major organic product(s) for each of the following reactions: 1) HNOZ/H, SO 2) Sn/HCl(aq) 3) HO 1) (CH3)2CHCI/AICI: 2) NBS/hv 1) Cly/FeCl3 2) HNO,/H2SO4 1) CH3CH,COCI/AICI 2) H20 оооооооо 3) Zn(Hg)/HCl(aq) 1) SOZ/H,SO 2) Bry/FeBrz 1) (CH3)3CCI/AICI: 2) KMnO/HOIA 2) H30* 1) CH,COCIAICI: 2) H, 3) Bry/FeBry COH 1) SOCI_/pyridine 2) PhCH/AICI 3) H20 1. Br JFeBry 2. Mg/Eto 3. oxirane 4, HO* 1) Bry/FeBry 2) s09/H230 1) NBS/hv 2) PhoNa (1 CH3COCI / AIC وا (2...
for c and d
2. Indicate the preferred product for the following reactions. (Include stereochemistry) HBr, CH 0OCH 1. PhCO,H 2. H'/CH OH H/KMnO Br2, H20
Indicate the preferred product for the following reactions.
Please show work-up.
2 H+/CH2OH
5. (7 pts) Predict the major product(s) for the following reactions. Remember to indicate stereochemistry, when appropriate. If no reaction is expected, write NR. C12 hv а. NBS hv b HBr ROOR с.
C. REACTIONS: (8 points each; 40 points total) For each of the following reactions or series of reactions, draw the final major organic product, reactant, or reagents in the box. Be sure to indicate STEREOCHEMISTRY where pertinent. In multiple step reactions, you may place intermediate products below the reaction for partial credit. 1. NH2 2. 1) NBS, hv 2) NaCN 0.5 eq 3) NaOH, H20 4) HCI 3. 1) NaBH4 2) MCPBA 3) NaOH 4) excess acetic acid, H+
6- Predict the product of the foliowing reactions. Assurme the Assume the necessary work up. (5pts cachi) (2) NabH 1) NaNH2 Pent-1-yne 1)Sía2BH THE 2) H202, NaOH KMno4 20, neutral o, (CH3)2 Hot, KMnO Acidic
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
Give the major product for the following reactions when
N-ethylaniline reacts with each of the following. Show the complete
reaction for each. Assume proper work-up.
a) HCl b) CH,COOH c) (CH),CO d) CH,CH,COCI e) Product in (d), then HNO, H.SO f) Product in (d), then [1] LAH and PH,0
Predict the major product/s formed in each of the following
reactions, indicate if the reagent reacts either regioselectively
or stereospecifically, or both in relevant cases
2. Predict the major product/s formed in cach of the following reactions, indicate if the reagent reacts either regioselectively or stereospecifically, or both in relevant cases (5 x 2 10 points): Write product/s of the reaction using Fischer projection на (Z)3-methyl-pent-2-ene .Write product/s of the reaction using Fischer projection. Br2 Write product/s of the reaction...