2.
Help, this got me really
confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS
Homework Answers
Gilmanns reagent R2CuLi undergo conjugate addition with enone.
Suzuki coupling reaction occurs between aryl borates and aryl/alkyl halides.
Wolff kishnner Reduction convert the ketone into alkane.
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2.Help, this got me really
confused. ORGANIC CHEMISTRY 353 UPPER LEVEL. THANKS
6. (21 pts.) Fill...
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...
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
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 =
whoever can help, it would be amazing! 353 organic chemistry upper level. 10. (3 pts.) Which statement best describes th...
whoever can help, it would be amazing! 353 organic chemistry
upper level.
10. (3 pts.) Which statement best describes the value of using an enamine vs. an enolate in synthesis? a) An enamine is acidic b) Enamines are more volatile and can be removed from solution more easily c) Enamine formation does not require a very strong base d) Enamines can be formed from tertiary amines 11. (6 pts.) Circle the major product for the reactions below: NH2 NH2 NH2...
Queston 6 (56 pts.). Provide the missing major organic products, or reagents/conditions, or organic reactants, as...
Queston 6 (56 pts.). Provide the missing major organic products, or reagents/conditions, or organic reactants, as appropriate. Do not forget to include stereochemistry as appropriate unless specified otherwise. 2. Hgo :0: :o 1. Na* CN 2. H30* /heat gnore stereochemistry c) :Br: :OH d) 1 Equiv H3C CI: e) Ph h) heat (Aldol reaction)
Organic chemistry 352. please help me. thanks! 1 a. The anti-influenza drug Tamiflu inhibits an enzyme involved in the r...
Organic chemistry 352. please help me. thanks!
1 a. The anti-influenza drug Tamiflu inhibits an enzyme involved in the release of new flu viruses from a host cel. When taken, Tamiflu does not become active until it reaches the liver, where it is hydrolyzed by an esterase Esterases are enzymes that catalyze the hydrolysis of esters. Draw the organic products formed when the ester group of tamiflu is hydrolyzed. Assume acidic conditions H/HO) Hio CHCH2) CHO 0 Tamiflu b. A...
Really really confused about this problem.Please tell me the answer as specific as possible!Thanks! 2. Answer...
Really really confused about this problem.Please tell me the
answer as specific as possible!Thanks!
2. Answer the following based on the table below which is the cost of one of many identical firms in a perfectly competitive market. Assume the good can only be produced in whole quantities (ie q = 4.7 not possible). All given numbers in the table are exact. (No rounding). Also assume that the amount of capital the firm is stuck with in the SR to...
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...
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
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 =
whoever can help, it would be amazing! 353 organic chemistry
upper level.
10. (3 pts.) Which statement best describes the value of using an enamine vs. an enolate in synthesis? a) An enamine is acidic b) Enamines are more volatile and can be removed from solution more easily c) Enamine formation does not require a very strong base d) Enamines can be formed from tertiary amines 11. (6 pts.) Circle the major product for the reactions below: NH2 NH2 NH2...
Queston 6 (56 pts.). Provide the missing major organic products, or reagents/conditions, or organic reactants, as appropriate. Do not forget to include stereochemistry as appropriate unless specified otherwise. 2. Hgo :0: :o 1. Na* CN 2. H30* /heat gnore stereochemistry c) :Br: :OH d) 1 Equiv H3C CI: e) Ph h) heat (Aldol reaction)
Organic chemistry 352. please help me. thanks!
1 a. The anti-influenza drug Tamiflu inhibits an enzyme involved in the release of new flu viruses from a host cel. When taken, Tamiflu does not become active until it reaches the liver, where it is hydrolyzed by an esterase Esterases are enzymes that catalyze the hydrolysis of esters. Draw the organic products formed when the ester group of tamiflu is hydrolyzed. Assume acidic conditions H/HO) Hio CHCH2) CHO 0 Tamiflu b. A...
Really really confused about this problem.Please tell me the
answer as specific as possible!Thanks!
2. Answer the following based on the table below which is the cost of one of many identical firms in a perfectly competitive market. Assume the good can only be produced in whole quantities (ie q = 4.7 not possible). All given numbers in the table are exact. (No rounding). Also assume that the amount of capital the firm is stuck with in the SR to...
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