please explain the work for both questions please
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please explain the work for both questions please
1. Predict the major organic product for each...
can you help me explain these especially number 2 Predict the major organic product for each...
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...
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
please explain the work 3. Predict the major product for the following elimination reaction. Make sure...
please explain the work
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. KOt-Bu t-BuOH 4. Draw a dibromide with molecular formula C14H12Br2 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 Newman projection. KOt-Bu t-BuOH
please explain the work 5. 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
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash...
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
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
For each of the following reactions: (1) Draw all of the organic product(s) that would be...
For each of the following reactions: (1) Draw all of the organic product(s) that would be formed, and (2) label each product as formed via S1, S2. E1, or E2. For elimination products, label as major or minor. Pay close attention to regiochemistry, stereochemistry, and whether carbocation rearrangements would occur. - DBN ci Br H20 B A C CH3OH acetone NaOH D Br DMSO
For the first six blanks, please choose only options from the dropdown menus provided below the...
For the first six blanks, please choose only options from the
dropdown menus provided below the pictures.
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
CH3OH ~ ??? Br - în...
Question 1 Predict the major product(s) for each of the following reactions. Show both enantiomers if...
Question 1 Predict the major product(s) for each of the following reactions. Show both enantiomers if a racemic mixture is formed: 1) MCPBA 2) H3O 1) BH3 THF 2) H202 NaOH HBr Br, H2 Pt
please answer all 1. Draw the structure of the principal organic product and predict the stereochemistry...
please answer all
1. Draw the structure of the principal organic product and predict the stereochemistry to be expected from the reaction of (IR, 2R)-1-bromo-2-methylcyclohexane with each of the following: a. NaOCH, in CH,OH at 60° d. NaNH, in NH, at 50° b. aqueous CH,OH at 140° e. aqueous CH,CH,OH at 25° c. Nal in DMSO at 40° 2. Draw the major product(s) (showing appropriate stereochemistry when necessary) for the following reactions. Indicate the mechanism(s) in operation (SNI, SN2, E1,...
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...
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
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. KOt-Bu t-BuOH 4. Draw a dibromide with molecular formula C14H12Br2 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 Newman projection. KOt-Bu t-BuOH
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
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
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
For each of the following reactions: (1) Draw all of the organic product(s) that would be formed, and (2) label each product as formed via S1, S2. E1, or E2. For elimination products, label as major or minor. Pay close attention to regiochemistry, stereochemistry, and whether carbocation rearrangements would occur. - DBN ci Br H20 B A C CH3OH acetone NaOH D Br DMSO
For the first six blanks, please choose only options from the
dropdown menus provided below the pictures.
Dropdown Menus:
1. methyl, primary (unhindered), primary (hindered), secondary,
tertiary
2. poor, weakly basic, strongly basic (hindered), strongly basic
(unhindered)
3. protic, aprotic
4. SN2, SN1, E1, E2, SN2 AND E2, SN1 AND E1, No Reaction
5. randomized, inverted, predictable but not inverted,
unchanged
6. a planar carbocation intermediate, backside attack transition
state, anti-periplanar transition state, other
CH3OH ~ ??? Br - în...
Question 1 Predict the major product(s) for each of the following reactions. Show both enantiomers if a racemic mixture is formed: 1) MCPBA 2) H3O 1) BH3 THF 2) H202 NaOH HBr Br, H2 Pt
please answer all
1. Draw the structure of the principal organic product and predict the stereochemistry to be expected from the reaction of (IR, 2R)-1-bromo-2-methylcyclohexane with each of the following: a. NaOCH, in CH,OH at 60° d. NaNH, in NH, at 50° b. aqueous CH,OH at 140° e. aqueous CH,CH,OH at 25° c. Nal in DMSO at 40° 2. Draw the major product(s) (showing appropriate stereochemistry when necessary) for the following reactions. Indicate the mechanism(s) in operation (SNI, SN2, E1,...
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