please explain the work 3. Predict the major product for the following elimination reaction. Make sure...
please explain the work 5. Predict the major product for the following elimination reaction. Make sure that you draw any relevant chair conformers to support your answer. KOt-Bu H3C CH3 t-BuOH CH3 6. Draw a cycloalkyl bromide with molecular formula C7H13Br that would give exclusively the following alkene under E2 reaction conditions. Use wedges and/or hashes to show the relative stereochemical relationships between groups, and support your answer with a relevant chair structure. CH3 KOt-Bu t-BuOH
Can you explain these 2 especially how you will know the leaving groups... please only answer if you know the correct answer. I will rate 3. Predict the major product for the following elimination reaction. Make sure that you draw any relevant Newman projections (looking down the C3-C4 bond) to support your answer. КО-Bu Hас" ён, t-BuOH 1 Draw a dibromide with molecular formula Ci4H12Br2 that would give exclusively the following alkene 4. under E2 reaction conditions. Use wedges and/or...
Pleaseee only answer if you know the right answer.. I will rate 5. Predict the major product for the following elimination reaction. Make sure that you draw any relevant chair conformers to support your answer. Ts KOt-Bu H3C "ICH3 t-BuOH CH3 6. Draw a cycloalkyl bromide with molecular formula C7H13Br that would give exclusively the following alkene under E2 reaction conditions. Use wedges and/or hashes to show the relative stereochemical relationships between groups, and support your answer with a relevant...
please explain the work 1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. Br H3CY CH3 NaOCH3. CH3OH OH يلي H2SO4 ما H3c OTS KOt-Bu t-BuOH AgNO3 H20 Ph HC, NaOH H2O OH H2SO4
please explain the work for both questions please 1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word “racemic” under any compound that is formed as a racemic mixture. Br AgNO3 H2O KOt-Bu H3CCH3 H36Br t-BuOH OTS NaOCH3 CH3OH CH3 NaOH H20 2. Draw all possible E2...
can you help me explain these especially number 2 Predict the major organic product for each of the following elimination reactions, and indicate 1. whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" under any compound that is formed as a racemic mixture. g. Br AgNO3 Нао h. HасСНз KOt-Bu Hас Br t-BuOH ф- Draw all possible E2 products (including...
2. For each reaction below, please draw the starting material or the major (singular) product, including any pertinent stereochemical details. (3 pts each) 1.TSCI 2. K ES 3. Hg(OAC)2, D20 -OH EtsN t-B 4. NaBH4 3. CHBrg 1. HBr ROOR 2. LDA THE Kot-Bu, t-BuOH 1. og 2. Me,s
2P (a) Draw/predict the major elimination product(s) of the following proposed reaction. Be sure to indicate correct stereochemistry when appropriate in the product. (b) Provide a mechanism that describes the formation of your drawn product. Show how (Newman Projection) any stereochemistry within the mechanism/product results. CHз Br NAOCH3 "CH-CHз
1. [10 pts] Consider the elimination reaction for the following alkyl halide with sodium methoxide in methanol (Na* OCH, CH,OH). CH NaOme MeOH CH Compound A Problem 2c Draw the major expected organic product (a) Redraw Compound A as seen in Viewpoint I below left as a Newman projection on the template provided in Problem 2a (below). Hint: Fill in missing Hs ar C2 and C3 to help you get started! (b) Rotate the C2 C3 bond to obtain the...
CHEM 301 Problem Set #5 2. Draw/predict the major elimination product(s) of the following proposed reaction. Be sure to indicate correct stereochemistry when appropriate in the product. (b) Provide a mechanism that describes the formation of your drawn product. Show how (Newman Projection) any stereochemistry within the mechanism/product results. CH e Br NaOCH **CH2CH, 3. Explain briefly, why neither an SNI nor SN2 reaction between diethyl ether and sodium iodide is favored but an Sw2 reaction between diethyl ether and...