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Chapter 15: Q68. (page 570)

Question: What monomer is needed to form each polymer?

a.

b.

Short Answer

Expert verified

Answer

a.

b.

Step by step solution

01

Monomer

Simple molecules comprising two or several binding sites called monomers. Examples are alkenes and vinyl chloride.

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Most popular questions from this chapter

Consider the following Bromination:

(a) Calculate ΔH° for this reaction by using the bond dissociation energies in Table 6.2.

(b) Draw out a stepwise mechanism for the reaction, including the initiation, propagation, and termination steps.

(c) Calculate ΔH° for each propagation step.

(d) Draw an energy diagram for the propagation steps.

(e) Draw the structure of the transition state of each propagation step

Question. Devise a synthesis of hexane-2,3-diol from propane as the only source of carbon atoms. You may use any other required organic or inorganic reagents.

Question: Consider the following Bromination:

(CH)3 CH +Br2→∆(CH3)3 CBr +HBr

(a) Calculate ΔH° for this reaction by using the bond dissociation energies in Table 6.2. (b) Draw out a stepwise mechanism for the reaction, including the initiation, propagation, and termination steps. (c) Calculate ΔH° for each propagation step. (d) Draw an energy diagram for the propagation steps. (e) Draw the structure of the transition state of each propagation step.

Question: Although CH4 reacts with Cl2 to form CH3Cl and HCl, the corresponding reaction of CH4with l2does not occur at an appreciable rate, even though the bond is much weaker than the bond. Explain why this is so.

Question: Devise a synthesis of CH2 CH2CH2CH2Br from HC≡CH You may use any other required organic or inorganic reagents.

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