(a)
Interpretation: The rigid or stronger
Concept introduction: The hydrogen bonding, the resonance effect, and the shorter bond length increase the stability of the polymer and hence the polymer becomes more rigid.
To determine: The rigid or stronger polymer from the polymer of ethylene glycol and teraphthalic acid and the polymer of
(b)
Interpretation: The rigid or stronger polymer from the given pair of the polymer is to be identified.
Concept introduction: The hydrogen bonding, the resonance effect, and the shorter bond length increase the stability of the polymer and hence the polymer becomes more rigid.
To determine: The rigid or stronger polymer from the polymer of
(c)
Interpretation: The rigid or stronger polymer from the given pair of the polymer is to be identified.
Concept introduction: The hydrogen bonding, the resonance effect, and the shorter bond length increase the stability of the polymer and hence the polymer becomes more rigid.
To determine: The rigid or stronger polymer from the polyacetylene and polyethylene.

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Chapter 21 Solutions
EBK CHEMISTRY: AN ATOMS FIRST APPROACH
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forward
- Synthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forward
- Indicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forward
- Question 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are reacted with sodium ethoxide in ethanol.arrow_forward
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