For the following reaction: a) Complete the reaction schemes by drawing the appropriate reagents and/or products...
Complete the following reaction sequences by drawing the major products or the reagents necessary to make them. Be sure to include stereochemistry when appropriate. 1. (48 pts) Complete the following reaction sequences by drawing the major products or the reagents necessary to make them. Be sure to include stereochemistry when appropriate. HBr Benzene FeBr3 HO NaH DMF hv NaNH2 2 BnBr CH2Cl2 Benzene Br2 cat. H+ H2o Ph NaOH NBS H Br H20 hv
Any help is appreciated!! 1) The following three schemes are missing reagents or products. Each missing reagent is 2 pts, each missing product is 3 pts. Do not add any reagents if something is already specified. Each scheme is independent. mCPBA DMP HN 2) Draw the mechanism of the acyl substitution reaction shown below. (8 pts)
Complete the following reaction sequences by drawing the major products or reagents needed to make them. 2. (2 4 pts) Complete the following reaction sequences by drawing the major products or the reagents necessary to make them. Be sure to include stereochemistry when appropiate Br2 H20 Br HBr NaNH2 b. H202 m-CPBA c.
The instructions say: Complete the following reaction sequences by drawing the major products or the reagents necessary to make them. Be sure to include stereochemistry when appropriate. reagents necessary to make them. Be sure to include stereochemistry when appropriate H2 (8) H2o Lindlar's cat Br 04 NaOEt b. CH2Cl2 DMSO NaNH Br NaOEt d. EtOH Br2 KOr-Bu MeOH HOr-Bu OH H2 (g) Pd /C
1) The following three schemes are missing reagents or products. Each missing reagent is 2 pts, each missing product is 3 pts. Do not add any reagents if something is already specified. Each scheme is independent. mCPBA Ą — men of — Toque — 29 - - Y- DMP - -
(32 pts) Complete the following reaction sequences by drawing the major products or the reagents necessary to make them. Be sure to include stereochemistry when appropriate. 2. NaOEt 'Br DMF EtOH, Δ Br 2 Cl Cl Cl HO Br Cl Cl H2 (8) Lindlar's cat.
asap 7. Base your answers to the following questions on the reactions or schemes below 0-0. +HO- For this reaction, equilibrium favors the products over the reactants. Explain why a. b. For the propagation step, this is a "guided" mechanism. I gave you all the reagents and products, just add in the arrows where appropriate! ONR2O-NR2 The termination step is also incredibly strange here. The following occurs either radically or ionically, but we aren't sure yet. At the very least,...
(30 pts) (a) Complete the following reactions by drawing the major products or the reagents to make them. (b) Label each reaction as Sy1.S2, El, E2, or addition. Be sure to 1. KOMe b. HOMe H20 d. MeOH cat. H Cl EtoH Cl
6. (15 points) Complete the following reaction schemes by providing the necessary product, starting material, and/or reagents in the boxes provided. Be sure to note any regio- and/or stereocontrol in the reaction. HO* 1. BH, THE 2.H2O, OH, H,0 HCEC: THE (solvent) 7. (4 points) Answer the following by providing the missing term in the space provide. order kinetics in the rate a. SN2 mechanisms are so named because they show determining step. intermediate, which can rearrange during the b....
3. (a) Consider the reaction Provide a mechanism scheme below. Provide a suitable reagent to complete the first step reagent (b) Provide a detailed mechanism for the transformation below 3. (a) Consider the reaction Provide a mechanism scheme below. Provide a suitable reagent to complete the first step reagent (b) Provide a detailed mechanism for the transformation below