organic chemistry 353, show the mechanism in detail please.
thanke you
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organic chemistry 353, show the mechanism in detail please.
thanke you
8. (18 pts.) Complete two...
help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 8. (18 pts.) Complete...
help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
8. (18 pts.) Complete two of the three multistep syntheses below. You will not recieve extra credit for doing all three. You do not need to provide an arrow pushing mechanism. Be as specific as possible and draw a star next the two you would like me to grade. e =
need help 1. (16 pts.) Complete two of the three multistep syntheses below. You will not...
need help
1. (16 pts.) Complete two of the three multistep syntheses below. You will not recieve extra credit for doing all three. You do not need to provide an arrow pushing mechanism. Be as specific as possible and draw a star next the two you would like me to grade. Mind your stereochemistry. -OH = -ОН HEH - -Li
5.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 9. (15 pts.) A)...
5.help, this got me really
confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS
9. (15 pts.) A) circle the more likely product of the reaction below B) provide an arrow-pushing mechanism for the entire reaction including electrophile formation C) draw three resonance structures of the intermediate justifying your answer to part A OMe ОMe Оме HNO H, SO NOZ
Organic Chemistry 2 Please show detailed arrow-pushing mechanism. Best regards. C) Please concisely explain how the...
Organic Chemistry 2
Please show detailed arrow-pushing
mechanism.
Best regards.
C) Please concisely explain how the below homo-aldol reaction can proceeds in the absence of a strong enough base. You also need to explain why the amine can be catalytic. (6 points, no mechanism needed, but a key intermediate might help). 'NH 10 CH3 CH3
organic chemistry 353 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution...
organic chemistry 353
2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): SO3H OH e 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. n Briefly describe w 4. (5 pts. Provide an example of an EAS reaction creates an arene that is less reactive than benzene (be specific, include reagents, you do not need to show the mechanism)
3.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 1. (4 pts) Arrange...
3.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
4.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS 1. (4 pts) Arrange...
4.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
Organic Chemistry 2 Please show detailed arrow-pushing mechanism. Best regards. 8) 20 points total. A) 10...
Organic Chemistry 2
Please show detailed arrow-pushing
mechanism.
Best regards.
8) 20 points total. A) 10 points: Please fill in the box with the appropriate product. Provide the mechanism for the second step. 5% no OOH 'N OH 21 50% QOH AcОН. Şo
Topic: Organic Chemistry Please make all drawings very clear. Please show all work and side products...
Topic: Organic Chemistry Please make all drawings very clear.
Please show all work and side products along with brief
explanations. Thank you.
4. Provide a complete curved-arrow mechanism for the transformation shown below. You do not need to account for any stereochemistry in your mechanism NH2 Me Me HO Ph Мео pH 5 O Ph
Organic Chemistry 2 Please show detailed arrow-pushing mechanism. Best regards. D) The following intramolecular Claisen can...
Organic Chemistry 2
Please show detailed arrow-pushing
mechanism.
Best regards.
D) The following intramolecular Claisen can give 2 possible products, however only one is observed. Please draw both in the appropriate box. Then, explain in less than 2 sentences and 2 structures why we only get the major product 7 points.. (1 point per box, 5 points for the explanation, 7 points total section). box. Then, explain in less than 2 mo XS NaoMe Meo moo n ome MeoH OMe...
help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
8. (18 pts.) Complete two of the three multistep syntheses below. You will not recieve extra credit for doing all three. You do not need to provide an arrow pushing mechanism. Be as specific as possible and draw a star next the two you would like me to grade. e =
need help
1. (16 pts.) Complete two of the three multistep syntheses below. You will not recieve extra credit for doing all three. You do not need to provide an arrow pushing mechanism. Be as specific as possible and draw a star next the two you would like me to grade. Mind your stereochemistry. -OH = -ОН HEH - -Li
5.help, this got me really
confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS
9. (15 pts.) A) circle the more likely product of the reaction below B) provide an arrow-pushing mechanism for the entire reaction including electrophile formation C) draw three resonance structures of the intermediate justifying your answer to part A OMe ОMe Оме HNO H, SO NOZ
Organic Chemistry 2
Please show detailed arrow-pushing
mechanism.
Best regards.
C) Please concisely explain how the below homo-aldol reaction can proceeds in the absence of a strong enough base. You also need to explain why the amine can be catalytic. (6 points, no mechanism needed, but a key intermediate might help). 'NH 10 CH3 CH3
organic chemistry 353
2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): SO3H OH e 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. n Briefly describe w 4. (5 pts. Provide an example of an EAS reaction creates an arene that is less reactive than benzene (be specific, include reagents, you do not need to show the mechanism)
3.Help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
4.help, this got me really confused. ORGANIC CHEMISTRY 353 UPPER
LEVEL. THANKS
1. (4 pts) Arrange the following compounds in order of increasing acidity (4 = most acidic): HH Meo OME 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): Br OMe 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. 4. (5 pts. Provide an example of an EAS reaction creates an arene that is...
Organic Chemistry 2
Please show detailed arrow-pushing
mechanism.
Best regards.
8) 20 points total. A) 10 points: Please fill in the box with the appropriate product. Provide the mechanism for the second step. 5% no OOH 'N OH 21 50% QOH AcОН. Şo
Topic: Organic Chemistry Please make all drawings very clear.
Please show all work and side products along with brief
explanations. Thank you.
4. Provide a complete curved-arrow mechanism for the transformation shown below. You do not need to account for any stereochemistry in your mechanism NH2 Me Me HO Ph Мео pH 5 O Ph
Organic Chemistry 2
Please show detailed arrow-pushing
mechanism.
Best regards.
D) The following intramolecular Claisen can give 2 possible products, however only one is observed. Please draw both in the appropriate box. Then, explain in less than 2 sentences and 2 structures why we only get the major product 7 points.. (1 point per box, 5 points for the explanation, 7 points total section). box. Then, explain in less than 2 mo XS NaoMe Meo moo n ome MeoH OMe...
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