Only need e and f Draw the structural formula (showing the repeating unit) for the product...
Draw the structural formula (showing the repeating unit) for the product of each polymerization reaction below. Then, choose 2 reactions and show the curved arrow mechanism for the polymerization You do not need to show termination, only initiation (if applicable) and propagation. You may abbreviate monomer and catalyst structures, as needed. ry + HCI — Mechanisms:
7. Draw the structural formula (showing the repeating unit) for the product of each polymerization reaction below. Then, choose 2 reactions and show the curved arrow mechanism for the polymerizati You do not need to show termination, only initiation (if applicable) and propagation. You abbreviate monomer and catalyst structures, as needed. Mechanisms:
The mechanism for number 2 please Polymers11 2. Write the reaction mechanism (showing arrows) of the synthesis of polystyrene. 4pts Include and show arrows in 2 initiation steps with benzoyl peroxide forming the phenyl radical. (this is shown in Figure 9 of the lab- just add all arrows) • A propagation step of the styrene (the monomer) and phenyl radical. • A second propagation step showing polymer growth by reacting styrene and the radical product of first propagation step. A...
Draw the bond line structural formulas for the products in the following reactions in the boxes provided (one structure per box). Where appropiate, clearly show stereochemistry. [2] e) HBr major product minor product [1.51 ) КОН ethanol НС" Br HC HCI Be prepared to provide structural formula for the starting reactants if given products *** (1 h) 1) O3 2) Zn, H20, H* Но 0 1) O3 2) Zn, H202 0 + [2] 1) KMnO4 141 8. Provide the missing...
CHE 230 F2019 Assignment 10 Student Name: ID Number: 10.W2S-1 Resonance structures of radicals: Draw two additional resonance structures for the molecule shown below. Be sure to show the curved arrows that demonstrate how you get from one resonance structure to the next. There should NOT be formation of partial charges in you structures. •H .U-I 10.W2S-2 When discussing radical reaction mechanisms we are concerned with bond strengths to make these mechanistic arguments. Which CH bond is the weakest in...
in LINE ANGLE format please Polymersti 2. Write the reaction mechanism (showing arrows) of the synthesis of polystyrene. 4pts • Include and show arrows in 2 initiation steps with benzoyl peroxide forming the phenyl radical. (this is shown in Figure 9 of the lab- just add all arrows) A propagation step of the styrene (the monomer) and phenyl radical. A second propagation step showing polymer growth by reacting styrene and the radical product of first propagation step. A termination step...
Draw a structural formula for the product of the aldol reaction of the compound shown above, as well as the a.B-unsaturated aldehyde or ketone formed from dehydration of the aldol product. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right comer. Separate structures using the sign from the drop-down menu. . o 1. Og 2. (CH3)2...
I need question 5 answered 4. The pk, of our product is- 2-3 units lower than the pK, of phenol. Two of seven resonance forms are shown. There are five additional resonance forms that are not shown. Those additional forms have the negative charge on a different atom than the one shown on the structures below. On one of resonance contributors shown, circle the other five atoms in the structure that will have a partial negative charge as a result...
QUESTIONS RELATE TO: HYDROCODONE 1. A.) Draw the expanded structural formula of HYDROCODONE (showing all atoms and all covalent bonds). If it contains atoms other than C or H add lone pairs of electrons to each until the octet rule is satisfied for that atom. B.) Determine molecular geometry of each central atom. C.) For each central atom decide if it is polar or non polar. 2. Illustrate all ways that hydrocodone molecule could form hydrogen bonds with water. Do...
A). 1-Heptene; B). 1-Propene ; C). 1-Butene ; D). CEN E). CH3NH2 ; F). -CO-H; G). CHỊCH,Br; H). NO, nyu, im Krui, ir CH3 OH Настен M H3C MC ;N HỌC-CH-CH, 0). an in the file can os centras 2005,8,0, Consider PHYSICAL PROPERTIES and the E/Z priority of the compounds/substituents above 1. Arrange in ascending order the boiling point and identify the non-covalent bonding : a)compound compounds Q, R, T, U; b) compound B, M, N c),arrange in ascending order...