Homework Answers
Add Answer to:
6. Cationic ring-opening polymerization of (S)-3- methyltetrahydrofuran with a catalytic amount of chlorosulfonic acid (HSO3CI) yields...
(21) 3. Consider the Ring Opening Metathesis Polymerization method: the initiating system in ring opening metathesis...
(21) 3. Consider the Ring Opening Metathesis Polymerization method: the initiating system in ring opening metathesis polymerization reactions. ring opening metathesis polymerization reactions. (C) Formulate a detailed mechanism for the ring opening metathesis polymerization reaction. (d) What is the major polymer product formed in the reaction of cyclopentene with the WCI/AIEt catalyst system? (e) Formulate a detailed reaction pathway for the reaction of cyclopentene with MoCls/AlEts catalyst system and draw the structure of the polymer product. (1) What is the...
6a (6 pts) Under the right conditions, ring opening of epoxides can form a polymerization. Draw...
6a (6 pts) Under the right conditions, ring opening of epoxides can form a polymerization. Draw the structure of the formed polymer using polymer notation in the box, and show the mechanism of initation and addition of two monomers below the reaction scheme. NaOMe 2 mmol 44 mmol b. (1 point) with the stoichiometry indicated above, what would "n" be equal to in the polymer? / 13 pts
When 3-methyl-1-butene is treated with a catalytic amount of BF3 and H2O a cationic polymerization process...
When 3-methyl-1-butene is treated with a catalytic amount of BF3 and H2O a cationic polymerization process occurs, but the expected homopolymer is not formed. Explain in detail with mechanism(s), intermediate structure(s) and the final repeat unit(s).
2. During the acid catalyzed polymerization of terephthalic acid and ethylene glycol, some fraction of methanol...
2. During the acid catalyzed polymerization of terephthalic acid and ethylene glycol, some fraction of methanol (CH-OH) is incorporated, but no more ester bonds can be formed. a. Based on the above, what is the extent of reaction, p? b. How does fav determine whether a linear or network polymer is formed as p nears 1? c. Why do you believe the polymer in this reaction will be a gel-network or linear chains? d. What is fivg, the average number...
3 Match the following polymer with the common product in which it is used (see intro...
3 Match the following polymer with the common product in which it is used (see intro for help). 1. polystyrene 2. nylon 3. polypropylene 4. low density polyethylene 5. polycarbonate a. Plastic Bags b. Water Pipes c. Cookware d. Egg containers e. Milk cartons 6. polyethylene f. Carpet and Knitted fabrics 7. polyvinylchloride 9. Automobile bumpers 8. polytetrafluoroethylene h. Rope 4. Shown below are monomers for common polymers that get made. Draw two repeating units of the polymer structure for...
please only do H-M. i have done everything else. 2. During the acid catalyzed polymerization of...
please only do H-M. i have done everything else.
2. During the acid catalyzed polymerization of terephthalic acid and ethylene glycol, some fraction of methanol (CH-OH) is incorporated, but no more ester bonds can be formed. a. Based on the above, what is the extent of reaction, p? b. How does fav determine whether a linear or network polymer is formed as p nears 1? c. Why do you believe the polymer in this reaction will be a gel-network or...
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use...
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate "acidic water"). (6 pts) 4. Draw a stepwise, detailed mechanism for the reaction below. Use curved arrows to indicate the flow of electrons. (Hint: think of this reaction as a combination of addition of HX (step 1) and hydration (step 2)]. In the second step, an...
need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an A...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
Unknown acid 2 6. Complete the following table. Trial 1 Trial 2 Trial 3 Mass of...
Unknown acid 2 6. Complete the following table. Trial 1 Trial 2 Trial 3 Mass of unknown (8) 0.175 0.120 0.122 Initial buret reading (mL) 0.00 22.37 0.00 Final buret reading (mL) 22.37 44.85 22.83 Volume of NaOH added (mL) 22.37 22.48 22.83 We will assume that the data collected for the first trial is not accurate. 7. What is the average mass of unknown acid for Trials 2 and 3? (Must show calculations) 8. What is the average volume...
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition...
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition of the proton to one face of the alkene with simultaneous delivery of a bromide ion from a different molecule of H-Br. 11. Which compound is the strongest nmucleophile for reaction of methane methanesulfonate (CHOS0.CH) in methanol at room temperature? (You may assume that everything is soluble in methanol) (A) potassium bromide (B) cesium iodide (C) sodiam chloride (D) lithium flaoride 12. Which proton...
(21) 3. Consider the Ring Opening Metathesis Polymerization method: the initiating system in ring opening metathesis polymerization reactions. ring opening metathesis polymerization reactions. (C) Formulate a detailed mechanism for the ring opening metathesis polymerization reaction. (d) What is the major polymer product formed in the reaction of cyclopentene with the WCI/AIEt catalyst system? (e) Formulate a detailed reaction pathway for the reaction of cyclopentene with MoCls/AlEts catalyst system and draw the structure of the polymer product. (1) What is the...
6a (6 pts) Under the right conditions, ring opening of epoxides can form a polymerization. Draw the structure of the formed polymer using polymer notation in the box, and show the mechanism of initation and addition of two monomers below the reaction scheme. NaOMe 2 mmol 44 mmol b. (1 point) with the stoichiometry indicated above, what would "n" be equal to in the polymer? / 13 pts
2. During the acid catalyzed polymerization of terephthalic acid and ethylene glycol, some fraction of methanol (CH-OH) is incorporated, but no more ester bonds can be formed. a. Based on the above, what is the extent of reaction, p? b. How does fav determine whether a linear or network polymer is formed as p nears 1? c. Why do you believe the polymer in this reaction will be a gel-network or linear chains? d. What is fivg, the average number...
3 Match the following polymer with the common product in which it is used (see intro for help). 1. polystyrene 2. nylon 3. polypropylene 4. low density polyethylene 5. polycarbonate a. Plastic Bags b. Water Pipes c. Cookware d. Egg containers e. Milk cartons 6. polyethylene f. Carpet and Knitted fabrics 7. polyvinylchloride 9. Automobile bumpers 8. polytetrafluoroethylene h. Rope 4. Shown below are monomers for common polymers that get made. Draw two repeating units of the polymer structure for...
please only do H-M. i have done everything else.
2. During the acid catalyzed polymerization of terephthalic acid and ethylene glycol, some fraction of methanol (CH-OH) is incorporated, but no more ester bonds can be formed. a. Based on the above, what is the extent of reaction, p? b. How does fav determine whether a linear or network polymer is formed as p nears 1? c. Why do you believe the polymer in this reaction will be a gel-network or...
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate "acidic water"). (6 pts) 4. Draw a stepwise, detailed mechanism for the reaction below. Use curved arrows to indicate the flow of electrons. (Hint: think of this reaction as a combination of addition of HX (step 1) and hydration (step 2)]. In the second step, an...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
Unknown acid 2 6. Complete the following table. Trial 1 Trial 2 Trial 3 Mass of unknown (8) 0.175 0.120 0.122 Initial buret reading (mL) 0.00 22.37 0.00 Final buret reading (mL) 22.37 44.85 22.83 Volume of NaOH added (mL) 22.37 22.48 22.83 We will assume that the data collected for the first trial is not accurate. 7. What is the average mass of unknown acid for Trials 2 and 3? (Must show calculations) 8. What is the average volume...
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition of the proton to one face of the alkene with simultaneous delivery of a bromide ion from a different molecule of H-Br. 11. Which compound is the strongest nmucleophile for reaction of methane methanesulfonate (CHOS0.CH) in methanol at room temperature? (You may assume that everything is soluble in methanol) (A) potassium bromide (B) cesium iodide (C) sodiam chloride (D) lithium flaoride 12. Which proton...
Most questions answered within 3 hours.
-
Calculate the equillibrium constent K for a redox reaction that
has E°cell = -.98 V at...
asked 9 minutes ago -
A concave spherical mirror has a radius of curvature of
magnitude 19.6 cm.
(a) Find the...
asked 10 minutes ago -
3. draw a diagram of the magnetic field:
a. around a long straight wire with a...
asked 9 minutes ago -
If you titrated 30.0 mL of 0.1 M HCl with 0.1 M NaOH, indicate
the approximate...
asked 18 minutes ago -
NADH passes electrons into the electron transport chain. List
the carriers that would receive the electrons,...
asked 26 minutes ago -
A cylindrical cable with a resistivity of 1.6x10-8 Ω·m and cross
sectional area of 3x10-5 m^2...
asked 26 minutes ago -
True or False.
A consumer with convex preferences who is indifferent between
the bundles (5,2) and...
asked 29 minutes ago -
A diamond's index of refraction for red light, 656 nm, is 2.410,
while that for blue...
asked 42 minutes ago -
Compare HPLC, SPE, and GC. Identify the differences, the
advantages, and the weaknesses of each method.
asked 43 minutes ago -
Characteristic x-rays emitted by potassium have a wavelength of
0.374 nm. What is the energy of...
asked 46 minutes ago -
there is a function to create two random numbers between 1 and
25 and a function...
asked 1 hour ago -
At a certain temperature, the ?pKp for the decomposition of
H2SH2S is 0.832.0.832.
H2S(g)↽−−⇀H2(g)+S(g)H2S(g)↽−−⇀H2(g)+S(g)
Initially, only...
asked 58 minutes ago