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Draw the structures
a Ng Nadime they! Soysamide b. propionic botyric anhydride c. Methyl cyclohexanê...
using the picture of the synthesis of methyl benzoate as a reference, name and draw the...
using the picture of the synthesis of methyl benzoate as a
reference, name and draw
the structure of the product of the reaction involving propionic
acid and isopropyl alcohol. Is the product a liquid or a
solid?
H2SO4 Y OH + H2C-OH 0 + H2O benzoic acid methanol benzoic acid methanol methyl benzoate methyl benzoate + H₂O OH propionic acid isopropyl alcohol
Q5: How will you convert the following? (0.5 mark each) a) Acetone to 2-methyl-2-propanol b) Acetone...
Q5: How will you convert the following? (0.5 mark each) a) Acetone to 2-methyl-2-propanol b) Acetone to 2-propanol c) Acetaldehyde to acetic acid d) Formaldehyde to 1-propanol e) Acetaldehyde to 2-butanol 1) Draw the structure of the following molecules i. Phenyl benzoate ii. Propanoic anhydride iii. Isopropyl acetate iv. 3-formylcyclopentane carboxylic acid v. 2,2-dimethylbutane dioic acid
1. There are three possible resonance structures of phenoxide; draw them and show electron pushing arrows....
1. There are three possible resonance structures of phenoxide; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid 2. There are three possible resonance structures of phenyl ethanoate, draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid 3. There are three possible resonance structures of methyl benzoate; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid
3. There are three possible resonance structures of methyl benzoate; draw them and show electron pushing...
3. There are three possible resonance structures of methyl benzoate; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid
Consider the resonance structures of acetanilide and methyl benzoate provided above. How does the -COOCH3 substituent on...
Consider the resonance structures of acetanilide and methyl
benzoate provided above.
How does the -COOCH3 substituent on methyl benzoate direct?
Do the partial charges shown on either acetanilide or
methyl-benzoate activate or deactivate the electrophilic
substitution reaction?
Is there a correlation between directing and activating groups?
Explain.
I
Resonance structures of methyl-benzoate and the resulting partial charges are shown below. How does the benzoate group direct? 0: -1 =O :00 00 OA Several resonance structures of acetanilide are shown below:...
Draw the reaction mechanism for the nitration of methyl benzoate to methyl nitrobenzoate, please show all...
Draw the reaction mechanism for the nitration of methyl benzoate to methyl nitrobenzoate, please show all resonance structures for each possible substitution position to explain why methyl m-nitrobenzoate was the favored isomer.
draw a mechanism for methyl 3 benzoate 2. For the nitration of methyl benzoate: Which product...
draw a mechanism for methyl 3 benzoate
2. For the nitration of methyl benzoate: Which product did you get? What evidence doyou have for this? Wasyourproduct pure? Whatevidence do you have for this? Explain your a. b. evidence. c. Draw the mechanism for the product you got. d. Calculate percent yield. Show your work
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne ...
Draw structures corresponding to the following names:
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
Give IUPAC names for the following compounds: Draw structures corresponding to each of the given names....
Give IUPAC names for the following compounds: Draw structures corresponding to each of the given names. A. 2-phenyl-2-propanol B. 2, 3-diphenyl-2-hexene C. 2-hydroxyacetophenone D. 5, 5-dimcthyl-l, 3, 6-cycloheptatriene-l-carboxylicacid E. Acetic anhydride
3. Draw the structures of each of the following molecules and then provide the reagents needed...
3. Draw the structures of each of the following molecules and then provide the reagents needed to convert each of the given starting materials into the required pro a) dimethyl sulfide dimethyl sulfoxide b) phenol methyl phenyl ether c) dimethyl ketone 2-propanol ㅡㅡ
using the picture of the synthesis of methyl benzoate as a
reference, name and draw
the structure of the product of the reaction involving propionic
acid and isopropyl alcohol. Is the product a liquid or a
solid?
H2SO4 Y OH + H2C-OH 0 + H2O benzoic acid methanol benzoic acid methanol methyl benzoate methyl benzoate + H₂O OH propionic acid isopropyl alcohol
Q5: How will you convert the following? (0.5 mark each) a) Acetone to 2-methyl-2-propanol b) Acetone to 2-propanol c) Acetaldehyde to acetic acid d) Formaldehyde to 1-propanol e) Acetaldehyde to 2-butanol 1) Draw the structure of the following molecules i. Phenyl benzoate ii. Propanoic anhydride iii. Isopropyl acetate iv. 3-formylcyclopentane carboxylic acid v. 2,2-dimethylbutane dioic acid
1. There are three possible resonance structures of phenoxide; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid 2. There are three possible resonance structures of phenyl ethanoate, draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid 3. There are three possible resonance structures of methyl benzoate; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid
3. There are three possible resonance structures of methyl benzoate; draw them and show electron pushing arrows. Then draw the overall resonance hybrid. (1 point) Hybrid
Consider the resonance structures of acetanilide and methyl
benzoate provided above.
How does the -COOCH3 substituent on methyl benzoate direct?
Do the partial charges shown on either acetanilide or
methyl-benzoate activate or deactivate the electrophilic
substitution reaction?
Is there a correlation between directing and activating groups?
Explain.
I
Resonance structures of methyl-benzoate and the resulting partial charges are shown below. How does the benzoate group direct? 0: -1 =O :00 00 OA Several resonance structures of acetanilide are shown below:...
draw a mechanism for methyl 3 benzoate
2. For the nitration of methyl benzoate: Which product did you get? What evidence doyou have for this? Wasyourproduct pure? Whatevidence do you have for this? Explain your a. b. evidence. c. Draw the mechanism for the product you got. d. Calculate percent yield. Show your work
Draw structures corresponding to the following names:
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
Give IUPAC names for the following compounds: Draw structures corresponding to each of the given names. A. 2-phenyl-2-propanol B. 2, 3-diphenyl-2-hexene C. 2-hydroxyacetophenone D. 5, 5-dimcthyl-l, 3, 6-cycloheptatriene-l-carboxylicacid E. Acetic anhydride
3. Draw the structures of each of the following molecules and then provide the reagents needed to convert each of the given starting materials into the required pro a) dimethyl sulfide dimethyl sulfoxide b) phenol methyl phenyl ether c) dimethyl ketone 2-propanol ㅡㅡ
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