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preditct the product and provide a rational mechanism
III). A. Predict the products for the following...
m). A. Predict the products for the following reaction and write a rational mechanism. HO -NH2...
m). A. Predict the products for the following reaction and write a rational mechanism. HO -NH2 (CH3CO)20 Mechanism:
m. A. Predict the products for the following reaction and write a rational mechanism. HO -NH2...
m. A. Predict the products for the following reaction and write a rational mechanism. HO -NH2 (CH3CO)20 Mechanism: M. B. The reaction of 5.30g of p-aminophenol with 15.20 g of acetic anhydride produced 4.35 g of acetaminophen. Calculate the percent yield of acetaminophen. m. C. How did you purify the crude acetaminophen? Briefly explain.
predit the products for the followig reaction and write a rational mechanism 1. A. Predict the...
predit the products for the followig reaction and write a
rational mechanism
1. A. Predict the products for the following reaction and write a rational mechanism. OCH (CH3CORO AICI: Mechanism:
1. A. Predict the products for the following reaction and write a rational mechanism. OCH3 (CH3CO20...
1. A. Predict the products for the following reaction and write a rational mechanism. OCH3 (CH3CO20 AICI: Mechanism: 1. B. Why are much larger quantities of aluminum chloride required for Friedel-Crafts acylation reactions than for alkylation reactions? T.C. A student reacted anisole with acetic anhydride in dichloromethane using aluminum chloride as a catalyst. The student used the experimental procedure as described in the laboratory manual. At the end of the experiment the student failed to get +- methoxyacetophenone. Give reasons...
help! chemistry predict the products and mechanism! the Product. Provide the stable organic product(s) for the...
help! chemistry predict the products and mechanism!
the Product. Provide the stable organic product(s) for the reactions below. predict the Pro 1. Mgº, CH,CH,OCH,CH 2. CO (9) 3. H,O, HCI MgBr (X) 2. H,0,HCI 1. K Cr2O, H,SO, H,0 2. CH, MgBr (1 eq.) 3. H2O, HCI 1. Mgº, CH,CH,OCHCH 2. H20, HCI echanism. The following Grignard reaction has been observed to yield products A and B. MgCI THF-70 C 2. HCI, H20 0. Org. Chem. 1980, 45, 4952-4954. https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01430)...
d for both of the questions 19-31 Predict the product(s) and provide the mechanism for each...
d for both of the questions
19-31 Predict the product(s) and provide the mechanism for each reaction below. What does each mechanism have in common? OH da + 19-32 Predict the product(s) and provide the mechanism for each reaction below. What does each mechanism have in common? HOOH H* catalyst HO OH (d) 0 Ht catalyst 7 CH3OH
1. Predict the product for the following reaction. Provide the mechanism for each reaction. Provide the...
1. Predict the product for the following reaction. Provide the mechanism for each reaction. Provide the sterochemistry and regiochemistry where is appropriate. HBr H2O Cat H+ HBr CHEM 2200-Spring 2020 Hydrohalogenation • Markovnikov orientation • Rearrangement can occur 2. Provide the product for the 2. Provide the product for the following reaction. Provide the sterochemistry and regiochemistry where is appropriate. Show the mechanism for C, and D. 0., b) a HC HCI HCI HBT -- "O HCI
Predict the product or provide the mechanism Predict the Product. Provide the stable organic product(s) for...
Predict the product or provide the mechanism
Predict the Product. Provide the stable organic product(s) for the reactions below. 1. Mgº, CH3CH,OCH CH3 2. CO2 (g) 3. H2O, HCI W MgBr (xs) 2. H2O, HCI 1. K Cr2O7, H2SO4, H2O 2. CH3MgBr (1 eq.) OH 3. H2O, HCI 1. Mgº, CH3CH2OCH2CH3 2. H2O, HCI Mechanism. The following Grignard reaction has been observed to yield products A and B. 1. Me Me MCI THF, -70 °C SOH OH ole er periodo...
7. Predict the major organic product or provide reagents needed to complete each reaction. 1. CH3NH2...
7. Predict the major organic product or provide reagents needed to complete each reaction. 1. CH3NH2 (a-b) excess 2. LIAIHA 3. H20 ia -NH ?? excess (c-d) HO NH2 triethylamine ? (e-f) CEN 1. CHẠMgBr 2. H20, H NH2 (g-h) H20, H* H2. Pd (1-1) CH3NH2 4 products (m) 1. LAIH 2. H2O, H & NH (n) 1. LiAIH4 2. H20, H+ 8. Predict the four possible Aldol condensation products and their dehydration products. KOH, H20.A + H 1. Predict...
26) Predict the major product for the following reaction and draw the full mechanism for product...
26) Predict the major product for the following reaction and draw the full mechanism for product formation (Hint: Aldol Condensation Reaction) 6 pts NaOH/H2O Heat Н. Bonus: Provide a step wise synthesis for the following conversions? 6 Pts (Multi step) wie Br A) OH OH NH2 B) OH C)
m). A. Predict the products for the following reaction and write a rational mechanism. HO -NH2 (CH3CO)20 Mechanism:
m. A. Predict the products for the following reaction and write a rational mechanism. HO -NH2 (CH3CO)20 Mechanism: M. B. The reaction of 5.30g of p-aminophenol with 15.20 g of acetic anhydride produced 4.35 g of acetaminophen. Calculate the percent yield of acetaminophen. m. C. How did you purify the crude acetaminophen? Briefly explain.
predit the products for the followig reaction and write a
rational mechanism
1. A. Predict the products for the following reaction and write a rational mechanism. OCH (CH3CORO AICI: Mechanism:
1. A. Predict the products for the following reaction and write a rational mechanism. OCH3 (CH3CO20 AICI: Mechanism: 1. B. Why are much larger quantities of aluminum chloride required for Friedel-Crafts acylation reactions than for alkylation reactions? T.C. A student reacted anisole with acetic anhydride in dichloromethane using aluminum chloride as a catalyst. The student used the experimental procedure as described in the laboratory manual. At the end of the experiment the student failed to get +- methoxyacetophenone. Give reasons...
help! chemistry predict the products and mechanism!
the Product. Provide the stable organic product(s) for the reactions below. predict the Pro 1. Mgº, CH,CH,OCH,CH 2. CO (9) 3. H,O, HCI MgBr (X) 2. H,0,HCI 1. K Cr2O, H,SO, H,0 2. CH, MgBr (1 eq.) 3. H2O, HCI 1. Mgº, CH,CH,OCHCH 2. H20, HCI echanism. The following Grignard reaction has been observed to yield products A and B. MgCI THF-70 C 2. HCI, H20 0. Org. Chem. 1980, 45, 4952-4954. https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01430)...
d for both of the questions
19-31 Predict the product(s) and provide the mechanism for each reaction below. What does each mechanism have in common? OH da + 19-32 Predict the product(s) and provide the mechanism for each reaction below. What does each mechanism have in common? HOOH H* catalyst HO OH (d) 0 Ht catalyst 7 CH3OH
1. Predict the product for the following reaction. Provide the mechanism for each reaction. Provide the sterochemistry and regiochemistry where is appropriate. HBr H2O Cat H+ HBr CHEM 2200-Spring 2020 Hydrohalogenation • Markovnikov orientation • Rearrangement can occur 2. Provide the product for the 2. Provide the product for the following reaction. Provide the sterochemistry and regiochemistry where is appropriate. Show the mechanism for C, and D. 0., b) a HC HCI HCI HBT -- "O HCI
Predict the product or provide the mechanism
Predict the Product. Provide the stable organic product(s) for the reactions below. 1. Mgº, CH3CH,OCH CH3 2. CO2 (g) 3. H2O, HCI W MgBr (xs) 2. H2O, HCI 1. K Cr2O7, H2SO4, H2O 2. CH3MgBr (1 eq.) OH 3. H2O, HCI 1. Mgº, CH3CH2OCH2CH3 2. H2O, HCI Mechanism. The following Grignard reaction has been observed to yield products A and B. 1. Me Me MCI THF, -70 °C SOH OH ole er periodo...
7. Predict the major organic product or provide reagents needed to complete each reaction. 1. CH3NH2 (a-b) excess 2. LIAIHA 3. H20 ia -NH ?? excess (c-d) HO NH2 triethylamine ? (e-f) CEN 1. CHẠMgBr 2. H20, H NH2 (g-h) H20, H* H2. Pd (1-1) CH3NH2 4 products (m) 1. LAIH 2. H2O, H & NH (n) 1. LiAIH4 2. H20, H+ 8. Predict the four possible Aldol condensation products and their dehydration products. KOH, H20.A + H 1. Predict...
26) Predict the major product for the following reaction and draw the full mechanism for product formation (Hint: Aldol Condensation Reaction) 6 pts NaOH/H2O Heat Н. Bonus: Provide a step wise synthesis for the following conversions? 6 Pts (Multi step) wie Br A) OH OH NH2 B) OH C)
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