Homework Answers
1,2 ethylene glycol and phthalic acid condense to give a monomer called glycol monophthalate with elimination of water. The glycol monophthalate has one -OH group at one end and one -COOH group at the other end. They polymerize with elimination of water as hydroxy group takes participate while acid group doesn't to give polyethylene phthalate which is a diestar.
The Modification of structure of ethylene glycol and
phthalic acid with elimination of water as shown as below.
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Polyethylene phthalate is a copolymer containing phthalic acid and ethylene glycol. Modify the molecules to show...
estion 14 of 14 Attemp For the dehydration shown, use curved arrows to show the formation...
estion 14 of 14 Attemp For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H,SOą, then draw the structure of the major product of the elimination. ОН H, SO product Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation the carbocation intermediate. Note: HSO, is formed from step 1, but not shown. Select Draw...
Modify the structures to show the bonds broken and formed in each acid-base reaction. Include counterions...
Modify the structures to show the bonds broken and formed in each acid-base reaction. Include counterions and charges where applicable. Modify the structures to show the products of Reaction A. Select Draw Rings More Erase H — a ISZ ZI + HCI Modify the structures to show the products of Reaction B. Select Draw Rings More Erase non li N -H + Lit-O-H - OH Modify the structures to show the products of Reaction C. Select Draw Rings More Erase...
Attempt 1 Question 7 of 9 > Butanone undergoes a nucleophilic addition with a Grignard reagent...
Attempt 1 Question 7 of 9 > Butanone undergoes a nucleophilic addition with a Grignard reagent made from 1-bromopropane and magnesium metal in THF solution. The alkoxide formed from the nucleophilic addition is then conveted into the final product by the careful addition of dilute acid. Complete the mechanism by following the instructions provided for each step.. Step 1. Nucleophilic Addition in THF Draw the alkoxide intermediate. Add a series of curved arrows to the sketch to demonstra a nucleophilic...
please tell me whats wrong in my answer, Im so confused. Modify the molecule to show...
please tell me whats wrong in my answer, Im so confused.
Modify the molecule to show the products formed by the hydrolysis of tripalmitoylglycerol. Add or remove atoms or bond as needed. Show all hydrogen atoms. Select Draw Rings More Erase VICONH I u H,C - OH Us HC OH HO CH UFU O 1. нс — он HO £ܝ @lala
acetlysalicycle acid question vities and Due Dates Ch 17 Assignment Score: 2400/2700 Resources C Give Up?...
acetlysalicycle acid question
vities and Due Dates Ch 17 Assignment Score: 2400/2700 Resources C Give Up? Hint Check Answer Question 21 of 27 > Attempt 4 Acetylsalicylic acid (aspirin) can be synthesized from salicylic acid and acetic acid in an acidic solution. COOH COOH CH3COOH HC + H2O salicylic acid acetylsalicylic acid (aspirin) Complete the structure of aspirin by removing the R substituent and drawing the correct functional group. Draw Select Rings Groups More Erase about us Careers privacy policy...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
estion 14 of 14 Attemp For the dehydration shown, use curved arrows to show the formation of the carbocation intermediate in the presence of sulfuric acid H,SOą, then draw the structure of the major product of the elimination. ОН H, SO product Step 1: Use curved arrows to complete the protonation mechanism of the alcohol. Step 2: Use a curved arrow to show the formation the carbocation intermediate. Note: HSO, is formed from step 1, but not shown. Select Draw...
Modify the structures to show the bonds broken and formed in each acid-base reaction. Include counterions and charges where applicable. Modify the structures to show the products of Reaction A. Select Draw Rings More Erase H — a ISZ ZI + HCI Modify the structures to show the products of Reaction B. Select Draw Rings More Erase non li N -H + Lit-O-H - OH Modify the structures to show the products of Reaction C. Select Draw Rings More Erase...
Attempt 1 Question 7 of 9 > Butanone undergoes a nucleophilic addition with a Grignard reagent made from 1-bromopropane and magnesium metal in THF solution. The alkoxide formed from the nucleophilic addition is then conveted into the final product by the careful addition of dilute acid. Complete the mechanism by following the instructions provided for each step.. Step 1. Nucleophilic Addition in THF Draw the alkoxide intermediate. Add a series of curved arrows to the sketch to demonstra a nucleophilic...
please tell me whats wrong in my answer, Im so confused.
Modify the molecule to show the products formed by the hydrolysis of tripalmitoylglycerol. Add or remove atoms or bond as needed. Show all hydrogen atoms. Select Draw Rings More Erase VICONH I u H,C - OH Us HC OH HO CH UFU O 1. нс — он HO £ܝ @lala
acetlysalicycle acid question
vities and Due Dates Ch 17 Assignment Score: 2400/2700 Resources C Give Up? Hint Check Answer Question 21 of 27 > Attempt 4 Acetylsalicylic acid (aspirin) can be synthesized from salicylic acid and acetic acid in an acidic solution. COOH COOH CH3COOH HC + H2O salicylic acid acetylsalicylic acid (aspirin) Complete the structure of aspirin by removing the R substituent and drawing the correct functional group. Draw Select Rings Groups More Erase about us Careers privacy policy...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
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