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(a)
Interpretation:
Reason behind for destruction of nylon using acids should be explained.
Concept introduction:
Nylon is a
Nylon 66 is synthesized from two monomers of hexamethylenediamine and adipic acid.
Molar mass (M):
A tripeptide is a combination of three amino acids joined together and forms peptide bonds.
(b)
Interpretation:
Reason behind for destruction of nylon using acids should be explained.
Concept introduction:
Nylon is a synthetic
Nylon 66 is synthesized from two monomers of hexamethylenediamine and adipic acid.
Molar mass (M):
A tripeptide is a combination of three amino acids joined together and forms peptide bonds.
(c)
Interpretation:
Reason behind for destruction of nylon using acids should be explained.
Concept introduction:
Nylon is a synthetic polymer, which is based on aliphatic or semi-aromatic polyamides.
Nylon 66 is synthesized from two monomers of hexamethylenediamine and adipic acid.
Molar mass (M):
A tripeptide is a combination of three amino acids joined together and forms peptide bonds.
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Chapter 23 Solutions
Chemistry: Atoms First
- Nonearrow_forwardTransmitance 3. Which one of the following compounds corresponds to this IR spectrum? Point out the absorption band(s) that helped you decide. OH H3C OH H₂C CH3 H3C CH3 H3C INFRARED SPECTRUM 0.8- 0.6 0.4- 0.2 3000 2000 1000 Wavenumber (cm-1) 4. Consider this compound: H3C On the structure above, label the different types of H's as A, B, C, etc. In table form, list the labeled signals, and for each one state the number of hydrogens, their shifts, and the splitting you would observe for these hydrogens in the ¹H NMR spectrum. Label # of hydrogens splitting Shift (2)arrow_forwardNonearrow_forward
- Draw the Lewis structure of C2H4Oarrow_forwarda) 5. Circle all acidic (and anticoplanar to the Leaving group) protons in the following molecules, Solve these elimination reactions, and identify the major and minor products where appropriate: 20 points + NaOCH3 Br (2 productarrow_forwardNonearrow_forward
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