1d.) Draw mechanism of cationic ring-opening polymerization of monomer M initiated with propargyl bromide and terminated with sodium hydroxide. Use special software for chemical drawings (e.g., ChemDraw, Biovia Draw, etc.) Response:
Q: Please re do over the work and check it it correct
A: Step 1: Basic mechanism of tautomerisation is: Step 2: The correct mechanism is: Mechanism C
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A: Approach to solving the question: Detailed explanation:The addition of the mercuric ion occurs with…
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Q: what is the mechanism of it?
A: Step 1:Step 2:Step 3: Step 4:
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Q: Determine the number of valence electrons in NH₂NH₂ and then draw the corresponding Lewis structure.
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A: Given:- Ksp for MgF2 = 6.4 × 10^-9- Initial concentration of magnesium nitrate [Mg(NO3)2] = 0.0304…
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A: Approach to solving the question: Detailed explanation: Examples: Key references:
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A: The question asks you to identify the correct acronym for a given molecule.The molecule in question…
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- 1 2 3 6 Polymer Sample # MW of 4 5 7 8 10 204 216 240 243 280 282 291 320 325 480 sample Compute (a) the number-average molecular weight, (b) the weight-average molecular weight, and (c) the degree of polymerization if the repeating unit have a molecular weight of 28g/mol (d) draw a polymer with 5 repeating units, based your monomer on the molecular weight Hint: Sort the weight ranges by 40.Draw the mechanism for ziegler-natta-catalyzed polymerization of a subdtitude ethylene.organic chem please help!! clear answer pls thank u
- Draw mechanism (with electron pairs, flow of electrons, charges, and steps, where applicable) of radical polymerization of styrene initiated by nitrile type initiator (RN=NR) that consists of initiation (two steps), propagation, and two termination steps (when two chains undergo combination and disproportionation reactions) Im stuck on how to show the mechanism for the two termination stepsmet 3) For the following reaction scheme below, a) draw the formed polymer and then by provide the initiation, propagation, and termination (using any reasonable termination method you lika) arrow. pushing mechanism for radical polymerization, D ARadical polymerization of styrene gives a linear polymer. Radical polymerization of a mixture of styrene and 1,4-divinylbenzene gives a cross-linked network polymer of the type shown in Figure 29.1. Show by drawing structural formulas how incorporation of a few percent of 1,4-divinylbenzene in the polymerization mixture gives a cross-linked polymer.
- Draw a chemical reaction scheme for the benzoyl peroxide-initiated polymerization of vinyl chloride showing the initiation, propagation and termination steps. The termination steps should include combination, disproportionation and transfer to initiator. (Assume that there is no secondary decomposition of primary radicals and that regioselective in the propagating step is 100% H-T).Methyl acrylate undergoes anionic polymerization using a variety of anionic initiators. Consider the reaction of methyl acrylate with a trace amount of tert-butyllithium. polymer Draw the curved arrow mechanism to show the initiation step, in which the tert-butanide anion acts as the initiator. Draw the curved arrow mechanism for the initiation step in the anionic polymerization of methyl acrylate. H C N 0 S F ClPlease answer 1 to 5. Thank yoouuu!!!!
- If u want helpful rating do it fast Terephthaloyl dichloride and p-phenylenediamine were polymerized to form a copolymer called Kevlar with M, of 250,000 g/mol. Calculate: C) Mw of the polymer(J) H H3C H a CH₂l2' Zn(Cu) Et2₂O CO₂Me b* H* H₂Odo both or else skip someonline will do all , i will upvote write in clean white paper