can you help me explain these especially number 2
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can you help me explain these especially number 2
Predict the major organic product for each...
please explain the work for both questions please 1. Predict the major organic product for each...
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...
please explain the work 1. Predict the major organic product for each of the following elimination...
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
Can you explain these 2 especially how you will know the leaving groups... please only answer...
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...
1. Predict the major organic product for each of the following reactions. Be sure to clearly...
1. Predict the major organic product for each of the following reactions. 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. B12 Ph Ph H20 H2 Pd/C OSO4 CH3 NMO H3C 1) Hg(OAC)2, H20 2) NaBH4, aq. NaOH CH3 812 CCl4 now any resposta Hac 1) BH3, THE 2) H2O2, aq. NaOH
16. Give the major product that you would expect to be formed in each of the...
16. Give the major product that you would expect to be formed in each of the following reactions. If you think there is no reaction write NR after the arrow. In each case give the mechanism (SN1, SN2, E1 or E2) by which the product is formed. Also indicate the correct stereochemistry when applicable. Both product and the mechanism should be correct to get credit. No partial credit. Nal -BuOK Acetone t-Buo NaSH DMF Br, H NaOMe DMSO MeOH,rt t-BuOH...
For letters h & i : For each of the following reactions, predict the major mechanistic pathway (SN1/SN2/E1/E2...
For
letters h & i :
For each of the following reactions, predict the major
mechanistic pathway (SN1/SN2/E1/E2) and the major organic
products
1. (cont.) (h) НСОН CHB -CHBr HCOH - (0) CH,CH,CH,CH,Br- NH 2. For each of the following indicate which reaction will occur faster. Explain your reasoning. (No credit will be given for guesses) (a) The reaction of (CH),CBr with 0.001M aqueous NaOH or 0.10M aqueous NaOH (b) The reaction of 2-bromobutane with NaOH in DMSO or NaSH...
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...
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
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...
1. Predict the major organic product for each of the following reactions. 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. B12 Ph Ph H20 H2 Pd/C OSO4 CH3 NMO H3C 1) Hg(OAC)2, H20 2) NaBH4, aq. NaOH CH3 812 CCl4 now any resposta Hac 1) BH3, THE 2) H2O2, aq. NaOH
16. Give the major product that you would expect to be formed in each of the following reactions. If you think there is no reaction write NR after the arrow. In each case give the mechanism (SN1, SN2, E1 or E2) by which the product is formed. Also indicate the correct stereochemistry when applicable. Both product and the mechanism should be correct to get credit. No partial credit. Nal -BuOK Acetone t-Buo NaSH DMF Br, H NaOMe DMSO MeOH,rt t-BuOH...
For
letters h & i :
For each of the following reactions, predict the major
mechanistic pathway (SN1/SN2/E1/E2) and the major organic
products
1. (cont.) (h) НСОН CHB -CHBr HCOH - (0) CH,CH,CH,CH,Br- NH 2. For each of the following indicate which reaction will occur faster. Explain your reasoning. (No credit will be given for guesses) (a) The reaction of (CH),CBr with 0.001M aqueous NaOH or 0.10M aqueous NaOH (b) The reaction of 2-bromobutane with NaOH in DMSO or NaSH...
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