Add the missing starting materials, reagents, or products
(aqueous work-up is assumed where necessary) Caution: Don't forget
to consider stereochemistry.
Add the missing starting materials, reagents, or products (aqueous work-up is assumed where necessary) Caution: Don't...
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+ OH CH,OH NaOH Meo NH2 room temp. HO OH Meo Me ОН Meo 2. Provide appropriate conditions to convert each of the following starting mana hexanoic acid (some transformations may require more than one step): It each of the following starting materials into OH OH ОMe "NH₂
3. Provide the reagents necessary to carry out the following reactions or provide the starting materials or major products of the following reactions, Indicate racemic mixtures where necessary. (39 pts) 1)AIC осн, a. Ph 2) PaC H Н,со 45 1) HS0, HNO b. 2) Pd/c. H Н,со он c. Ph HO, он
Complete the reactions by filling in the missing starting
materials, reagents, or products
2. NaNO2 HCI NO2 1. SnCl2 HCI HO3S CuBr
Please Print! 2. Fill in the missing reactants, reagents & conditions, or products. Show stereochemistry where appropriate. 10 points. MgBr OH then H30+ „CH₃ HAN CH3 Ht cat MgBr N-CH₃ Мео (then H30t Meo он NaCN -CH3 CH₃ OTS CN or CH "CH₃ +
2. Complete the following reaction schemes by giving the structure of the missing products, starting materials, or solvents. Give the correct stereochemistry where appropriate H, CCB KOH, DMF HE b. 5CHANH T B DMSO (CH),CLI THE CH2CH3 CICH,CH SNa aprotic solvents NaN SN
1. Provide the products, starting materials, or reagents. regioselectivity of the reactions. Use filled or dashed wedges, where appropriate. (0.6 pts) Be sure to consider both the stereoselectivity andior 21 H20 H20 [1] (sia)2BH H2SO4 HgSO4 12] NaOH, H202 CH3 2 HCI CH
(45 pts.) Provide anylall missing products or reactants foe the following reaction equaons All required reagents or catalysts mustbe included for ful credit. Clearly indicate proper stereochemistry and/oe regiochemistry where appropriate. If more than one isomer is possible all must be shown for full eredit. Mechanisms are not necessary, but my belp as a method of "sbowing work" for partial credit. b. H2S04 +H20 ? +Br Most stable configuration
What is the major organic product for #2,4,5?
On the synthesis what is the reagents, starting materials, and
intermediates?
the major organic product(s) of the following reactions. Indicate stereochemistry Reactions, Predict Where neAnswer 4 reactions below, 1 points each, 4 points total). bold and dashed wedges). Partial credit will be given to correct work so show 1. Excess CHal 3. Heat necessary (with NH2 1. NaNO2. HC 2. CuCN 2. Br 2. H2N-NH2 (CH3)2CHOH 1. PhCH2NH2 2. LiAIHA 5. Synthesis....
draw the starting material, intermediate, and products where
its necessary for the parts
Draw the required intermediate compound of the following chemical transformation on benzene. NH, NH AICI, intermediate 2. KOH, H, O heat Draw the product of the following reaction (TsOH is a strong acid): excess MeOH TsOH Along with cyclopentanone, draw the other reagent required to form the following compound. You can use organic or inorganic reagents as necessary. Bangunan naman dari setenga e lemente una campana wa...
4. Fill-in-the-blanks: draw the missing reactants or products involved in the following single or multi-step reactions. Indicate stereochemistry and draw multiple stereoisomers where applicable. i EtOH EtOH [H2SO4] 1) EtMgBr 2) H20 5. For most ketones, hydrate formation is unfavorable, because the equilibrium favors the ketone rather than the hydrate. However, the equilibrium for hydration of hexafluoroacetone favors the hydrate. Propose a mechanism for this transformation below and provide an explanation for this observation. H2O Но он F3CX CF3 F3C...