- 27.4.14: Draw a short segment of gutta-percha.
- 27.4.15: Draw a segment of the polymer that would be formed from 1,2-polymer...
Solutions for Chapter 27.4: POLYMERIZATION OF DIENES THE MANUFACTURE OF RUBBER
Full solutions for Organic Chemistry | 7th Edition
Compounds formed from just two elements. (2.7)
The intermolecular attraction between like molecules. (11.3)
A lipid that readily undergoes hydrolysis in aqueous acid or base to produce smaller fragments.
critical temperature (Tc).
The temperature above which a gas will not liquefy. (11.8)
Cyclic polyethers whose molecular models resemble crowns.
cubic close packing
A crystal structure where the atoms are packed together as close as possible, and the close-packed layers of atoms adopt a three-layer repeating pattern that leads to a face-centered cubic unit cell. (Section 12.3)
Elimination of water.
The measure of disorder associated with a system.
A reaction that has a rate equation in which the sum of all exponents is one.
Elements that are in the same column of the periodic table; elements within the same group or family exhibit similarities in their chemical behavior. (Section 2.5)
A protein, particularly rich in the basic amino acids lysine and arginine, that is found associated with DNA molecules
A rule stating that electrons occupy degenerate orbitals in such a way as to maximize the number of electrons with the same spin. In other words, each orbital has one electron placed in it before pairing of electrons in orbitals occurs. (Section 6.8)
A monosaccharide containing a ketone group.
A method for building a peptide from protected building blocks.
A way to view a molecule by looking along a carbon-carbon single bond
nuclear binding energy
The energy required to decompose an atomic nucleus into its component protons and neutrons. (Section 21.6)
Light oscillating in only parallel planes.
A macromolecule containing many amino acid units, each joined to the next by a peptide bond
The stabilization associated with the delocalization of electrons via resonance.
Stork enamine synthesis
A Michaelreaction in which an enamine functions as anucleophile.