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Please help with A.
7. Devise a synthesis of one of the targets below. Legal reagents...
A and B are the products. devise a synthesis to form on eof the two products....
A
and B are the products. devise a synthesis to form on eof the two
products.
7. Devise a synthesis of one of the targets below. Legal reagents are bromobenzene, toluene, acetophenone, benzaldehyde, benzoic acid, MVK, any cycloalkane of 6 C or less, any 2C or less monofunctional organic reagent, and any inorganic reagents. obry odno (+) (+/-)
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-...
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) он
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic...
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-...
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) other reagents glven) MS, Bones он
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons...
One-step synthesis: Design a synthesis, showing all of the reagents and products along the way. You...
One-step synthesis: Design a synthesis, showing all of the
reagents and products along the way. You may use any inorganic
reagent and any organic reagent of two carbons or less.
3) НО. НО ? + En
need help with this one Devise a stepwise synthesis for the compound below using any of...
need help with this one
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) он
Please explain the mechanisms! 1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Mu...
Please explain the mechanisms!
1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
**URGENT IR UNKNOWN: Please Identify the unknown molecule from the IR spectrum shown below. Pick one...
**URGENT IR UNKNOWN: Please Identify the unknown molecule from
the IR spectrum shown below. Pick one from the following from the
list of of possibilities for the unknown molecule:
(1,2-dimethoxybenzene, 1,3-propanediol, 1-bromobutane,
1-octanol, 2,3-dimethyl-2-butanol, 2-cyclohexen-1-one,
2-cylopenten-1-one, 2-methylcyclohexanone, 3,3-dimethyl-2-butanone,
3-ethyltolulene, 3-methyl-1-butanol, 4-benzylpiperidine,
4-methylphenol, N,N-dimethylformamide, N-methylaniline, Acetic
anhydride, Acetone, Acetonitrile, Acetophenone, Acetyl chloride,
Allyl alcohol, Anisole, Benzaldehyde, Benzoic acid, Benzophenone,
Benzoyl chloride, Benzyl acetate, Bromobenzene, Cyclohexanone,
Cyclopentanone,Cyclopropyl methyl ketone, Diethylamine,Dimethyl
malonate, Ethyl cyanoacetate, Gamma-butyrolactone, Heptanoic acid,
Methyl benzoate, Methyl propionate, Napthalene,
Nitrobenzene,O-xylene,...
Devise a synthesis of (Z)-2-butene using one of the starting materials and any of the reagents below using...
Devise a synthesis of (Z)-2-butene using one of the starting materials and any of the reagents below using the than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials HCECH HCEC-CH, HCEC-CH,CH, HCEC-CH,CH,CH, CH, сн. HC=C-C-CH сн. HC=C-C-CH CH₂ Reagents a NaNH / NH (0) diodo ethane | 1-bromo-3-methylbutane i Hz / Lindlar catalyst b NaOH/H20 e 1-bromopropane ht-butyl bromide k H / NH30) Clodomethane 2-bromopropane Hy / Pd on carbon Na / NH...
** URGENT IR UNKNOWN: Please Identify the unknown molecule from the IR spectrum shown below. Pick...
** URGENT IR UNKNOWN: Please Identify the unknown molecule from
the IR spectrum shown below. Pick one from the following from the
list of of possibilities for the unknown molecule:
(1,2-dimethoxybenzene, 1,3-propanediol, 1-bromobutane, 1-octanol,
2,3-dimethyl-2-butanol, 2-cyclohexen-1-one, 2-cylopenten-1-one,
2-methylcyclohexanone, 3,3-dimethyl-2-butanone, 3-ethyltolulene,
3-methyl-1-butanol, 4-benzylpiperidine, 4-methylphenol,
N,N-dimethylformamide, N-methylaniline, Acetic anhydride, Acetone,
Acetonitrile, Acetophenone, Acetyl chloride, Allyl alcohol,
Anisole, Benzaldehyde, Benzoic acid, Benzophenone, Benzoyl
chloride, Benzyl acetate, Bromobenzene, Cyclohexanone,
Cyclopentanone,Cyclopropyl methyl ketone, Diethylamine,Dimethyl
malonate, Ethyl cyanoacetate, Gamma-butyrolactone, Heptanoic acid,
Methyl benzoate, Methyl propionate, Napthalene,...
URGENT IR UNKNOWN: Please Identify the unknown molecule from the IR spectrum shown below. Pick one...
URGENT IR UNKNOWN: Please Identify the unknown molecule from the
IR spectrum shown below. Pick one from the following from the list
of of possibilities for the unknown molecule:
80 70 2109.74cm-1 3021.84cm-1 1598.19cm-1 60 3033.75cm-1 50 1070.67am-1 3058.02cm-1 3080 79am-1 40 30 1443.72cm-1 20 1488.33cm-1 1어 757.39cm-1 3291.90cm-1 -o- -2 4000 3500 3000 2000 2500 1500 1000 500450 cm-1 1,2-dimethoxybenzene (91-16-7) 1,3-propanediol (504-63-2) 1-bromobutane (109-65-9) 1-Octanol (111-87-5) 2,3-dimethyl-2-butanol (594-60-5) 2-cyclohexen-1-one (930-68-7) 2-cyclopenten-1-one (930-30-3) 2-methylcyclohexanone (583-60-8) 3,3-dimethyl-2-butanone (75-97-8) 3-ethyltoluene (620-14-4)...
A
and B are the products. devise a synthesis to form on eof the two
products.
7. Devise a synthesis of one of the targets below. Legal reagents are bromobenzene, toluene, acetophenone, benzaldehyde, benzoic acid, MVK, any cycloalkane of 6 C or less, any 2C or less monofunctional organic reagent, and any inorganic reagents. obry odno (+) (+/-)
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) он
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic...
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) other reagents glven) MS, Bones он
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons...
One-step synthesis: Design a synthesis, showing all of the
reagents and products along the way. You may use any inorganic
reagent and any organic reagent of two carbons or less.
3) НО. НО ? + En
need help with this one
Devise a stepwise synthesis for the compound below using any of the following reagents: cyclohex-2- enone, alcohols, alkenes, and/or alkynes of FOUR carbons or less, benzene, any inorganic reagents, any oxidizing or reducing agents, and any peroxyacids. DO NOT GIVE MECHANISMS. (Bonus: make your cyclohex-2-enone using only the other reagents given) он
Please explain the mechanisms!
1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
**URGENT IR UNKNOWN: Please Identify the unknown molecule from
the IR spectrum shown below. Pick one from the following from the
list of of possibilities for the unknown molecule:
(1,2-dimethoxybenzene, 1,3-propanediol, 1-bromobutane,
1-octanol, 2,3-dimethyl-2-butanol, 2-cyclohexen-1-one,
2-cylopenten-1-one, 2-methylcyclohexanone, 3,3-dimethyl-2-butanone,
3-ethyltolulene, 3-methyl-1-butanol, 4-benzylpiperidine,
4-methylphenol, N,N-dimethylformamide, N-methylaniline, Acetic
anhydride, Acetone, Acetonitrile, Acetophenone, Acetyl chloride,
Allyl alcohol, Anisole, Benzaldehyde, Benzoic acid, Benzophenone,
Benzoyl chloride, Benzyl acetate, Bromobenzene, Cyclohexanone,
Cyclopentanone,Cyclopropyl methyl ketone, Diethylamine,Dimethyl
malonate, Ethyl cyanoacetate, Gamma-butyrolactone, Heptanoic acid,
Methyl benzoate, Methyl propionate, Napthalene,
Nitrobenzene,O-xylene,...
Devise a synthesis of (Z)-2-butene using one of the starting materials and any of the reagents below using the than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials HCECH HCEC-CH, HCEC-CH,CH, HCEC-CH,CH,CH, CH, сн. HC=C-C-CH сн. HC=C-C-CH CH₂ Reagents a NaNH / NH (0) diodo ethane | 1-bromo-3-methylbutane i Hz / Lindlar catalyst b NaOH/H20 e 1-bromopropane ht-butyl bromide k H / NH30) Clodomethane 2-bromopropane Hy / Pd on carbon Na / NH...
** URGENT IR UNKNOWN: Please Identify the unknown molecule from
the IR spectrum shown below. Pick one from the following from the
list of of possibilities for the unknown molecule:
(1,2-dimethoxybenzene, 1,3-propanediol, 1-bromobutane, 1-octanol,
2,3-dimethyl-2-butanol, 2-cyclohexen-1-one, 2-cylopenten-1-one,
2-methylcyclohexanone, 3,3-dimethyl-2-butanone, 3-ethyltolulene,
3-methyl-1-butanol, 4-benzylpiperidine, 4-methylphenol,
N,N-dimethylformamide, N-methylaniline, Acetic anhydride, Acetone,
Acetonitrile, Acetophenone, Acetyl chloride, Allyl alcohol,
Anisole, Benzaldehyde, Benzoic acid, Benzophenone, Benzoyl
chloride, Benzyl acetate, Bromobenzene, Cyclohexanone,
Cyclopentanone,Cyclopropyl methyl ketone, Diethylamine,Dimethyl
malonate, Ethyl cyanoacetate, Gamma-butyrolactone, Heptanoic acid,
Methyl benzoate, Methyl propionate, Napthalene,...
URGENT IR UNKNOWN: Please Identify the unknown molecule from the
IR spectrum shown below. Pick one from the following from the list
of of possibilities for the unknown molecule:
80 70 2109.74cm-1 3021.84cm-1 1598.19cm-1 60 3033.75cm-1 50 1070.67am-1 3058.02cm-1 3080 79am-1 40 30 1443.72cm-1 20 1488.33cm-1 1어 757.39cm-1 3291.90cm-1 -o- -2 4000 3500 3000 2000 2500 1500 1000 500450 cm-1 1,2-dimethoxybenzene (91-16-7) 1,3-propanediol (504-63-2) 1-bromobutane (109-65-9) 1-Octanol (111-87-5) 2,3-dimethyl-2-butanol (594-60-5) 2-cyclohexen-1-one (930-68-7) 2-cyclopenten-1-one (930-30-3) 2-methylcyclohexanone (583-60-8) 3,3-dimethyl-2-butanone (75-97-8) 3-ethyltoluene (620-14-4)...
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