Using the following monomer: H2C CH C CH- CH CH CH C-F (the benzene ring does not react) draw the mechanism for the formation of the polymer, stopping after attaching three units of the monomer together. DETAIL!! You will need more than one reaction, and yes, this will be one time you need to consider the mechanism. (20 pt.)

pls help ill rate u

(75)  (75) Consider the following reaction.  From the given choices of intermediates and/or final products, choose the 5 related to this reaction and put them in order to describe the complete mechanism (all the steps involved) for this reaction.

26: d,e,f

Chemistry help with mechanism plz OH 2 CI S. H. NaOH Он Procedure

3. The thermal polymerization of B-carboxymethyl caprolactam proceeds by an initial isomerization via a second-order kinetic process followed by condensation of the isomer to the polymer: -NH -NH2 Isomerization Polymerization HO The data below were obtained at 270 °C for the polymerization of B-carboxymethyl caprolactam. t (min) c (mol fraction) 20 0.042 30 0.039 40 0.028 50 0.024 60 0.021 80 0.018 90 0.015 110 0.013 120 0.012 Given that the rates of polymerization are first order in vNH, and v(cO),0 and vNH, = V(CO),0 - (1) Using a graphical method, determine whether these data indicate catalyzed or uncatalyzed conditions, and evaluate the rate constant for the polymerization. (ii) Describe a method by which the values of c (mol fraction) might be determined. (Where vNH, and v(co),0 are the number of NH2 and (CO),0 functional groups.)

(e) Pure liquid styrene (phenylethene) is polymerized by adding a soluble peroxide initiator. When the initial monomer concentration is 2.07 M and the peroxide concentration is 2 x 104 M, the initial rate of polymerization (vp) is 2.49 x 103 M min . The rate constant for the decomposition of the initiator (k; ) is 5.7 x 103 min!. (i) Determine the ratio kp/ (kt). State any assumptions. (ii) Calculate the expected number average molecular weight assuming termination takes place by mutual termination only.

Please answer a-d!!! Thanks so much!

If I will use sulfuric acid to modify activated carbon, what will be the role of sulfuric acid in the activated carbon? (Will it add new functional groups? Will it enhance the surface area of activated carbon? etc.)    Why does sulfuric acid-modified activated carbon adsorb more pollutants, specifically antibiotics, in water compared to unmodified activated carbon?   Can someone draw a mechanism or the reaction for both questions? Thank you!

uncements les ments s ourse es ons 19 Draw the initiation, propagation, and two example termination steps for this reaction. Include these steps under the headings "initiation", "propagation", and "termination". With reference to your mechanism, which one of the two possible products shown is formed? Also, show two checks that your propagation steps are correct. CH₂SH CN CN H₂C-C-N-N-C-CH₂ CH₂ CH₂ Edit View Insert Format Tools Table 12pt Paragraph BI UA SCH3 or SCH₂ 2 T² :