A) Write the productes) for the following reactions Na CN +-Очок Na OE+ Br NaOET +...
Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (10 points total) Br HBr CH2CI Br2 HBr Но ROOR CH,OH Н,о н* Н,о° 1) Hg(O,CCF3)2 CH,OH 1) BН, THF 2) H,О, NaOH, Нао 2) NaBH, NaOH 1) Hg(OAc) Н0, THF/ Hа Pd/C 2) NaBH, NaOH
12. Draw all major products for the following reactions. Indicate any region specificity Mark, Non Mark, syn or anti addition were necessary. (36 points) HgSO H SO. Na NH 1.2 HB 2. cther R BH THE NaOH, HOA Bry CCL OH NaOCI HOAC o E HBr ROOR hy NBS, hy 1. Hg(OAC), H,O/THF 2. NaBHA Br 1. NaNH Br 1. LAIH 2. H0
Draw the major products for the following reactions below. Write no reaction if no reaction. Br NBS hy NO2 Br2 FeBr3 Cl2 FeCl3 НО, Nal O N НО, CI AICI: KMnO4
Draw the major product for the following reactions.
-OH 2. Draw the major product for the following reactions. 1) TSCI 2) NaOEt, Heat 3) O; 4) DMS 1) NBS, heat (I cq.) 2) NaNH, DMSO 3) KMnO4 (aq) NaOH, cold 4) NaOCI, acetic acid 1) O 2) H,0 3)NI, H, 150, 100 atm 1) RBH 2) H.O, NaOH 3) NBS, heat (I eq) 1) KMnO heat 2) Na, NH, CH OH 3) Bry, light (I eq) 1) NBS, light 2)...
1. Determine whether the following reactions go through SN or SNP and write the products, with stereochemistry as applicable. BrNHz NaOEt Nal OMS KCN CI DMSO Br HO NaSH DMSO Tso CH3 Nal Acetone CH3 2. The following reactions each undergo SNmechanisms. For each explain why you would predict the substitution products to come from an SN2mechanism and fill in the product. If stereochemistry is given in the reactants, give the correct stereochemistry in the products. Cl + Z Na...
can you please provide the major products reactions
with the stereochemistry. thank you
HBr оос CN NC Br2 ОН FeBrz НО ОН 1 н* CI он NaOCH Br Eto OEt
please help asap in all sections!!
Question 5 Methyl 4-methylpentanoate is one of 120 volatile compournds identified in a study of metabolites from Streptomyces bacteria (Actinomycetologica 2009, 23, 27-33) Mathy 4-methylpentanoate The synthesis of Methyl 4-methylpentanoate using 2-methylbutane involves several steps. Part-1 of the reaction scheme (2-methylbutane to 3-methyl-1-butene) is illustrated below. Identity the reagent involved in each step and arange them accordingly Br A by NaOH; Os and H20; HBr/ROOR; NaOEt/EtOH NaOH; O and HyO; NaDE/EROH; HBr/RDOR Br: NaOE/EOH;...
3. Draw the product(s) of the following reactions. You do not have to include stereochemistry. (2 points per box) uLi HBr kinetic 1.OH CN- 3. но 4. Draw the product of the following Diels-Alder reactions. Include stereochemistry as appropriate CN CN CO2Me
3. Draw the product(s) of the following reactions. You do not have to include stereochemistry. (2 points per box) uLi HBr kinetic 1.OH CN- 3. но 4. Draw the product of the following Diels-Alder reactions. Include stereochemistry as...
Predict the products of the following reactions.
Na, NH3 1 equivalent HBr f. Br NaNH2 (excess) Br g. 1. Sia BH, THF 2. H202, NaOH h. HgSO HSO HO I
What is the correct sequence of reactions that can achieve the
following multistep transformation?
List in the correct order. (No spaces nor commas in between
letters) eg: GAKJO
☺ > REAGENTS A Br2 B TosCl, pyr CHOH SO, cat DO Na 1 MeBr 2. EtBr 3. NaNH 1 eq E 1. OsO4 2. NaHSO3 F NaNHExcess GHO H NBS, hv I HBr ROOR L HBr M NaOtBu N NaOEt O NaoMe PETOH, H+ Cat Q NaCN RH, Lindlar's SH, Pt...