- 184.108.40.206: The boiling points of the 1,2-dichloroethylene stereoisomers are 47...
- 220.127.116.11: Octane and 2,2,3,3-tetramethylbutane have boiling points that diffe...
- 18.104.22.168: (a) The dipole moment of acetaldehyde is 2.7 D and that of propene ...
- 22.214.171.124: Within each set, arrange the compounds in order of increasing boili...
- 126.96.36.199: Label each of the following molecules as a hydrogen-bond acceptor, ...
- 188.8.131.52: Match the structures with the following melting points. Explain. 16...
- 184.108.40.206: If the sawtooth pattern of melting point behavior is explained by t...
Solutions for Chapter 8.5: homoGeneouS noncoValent intermolecular attractionS: boilinG pointS
Full solutions for Organic Chemistry | 6th Edition
Solutions for Chapter 8.5: homoGeneouS noncoValent intermolecular attractionS: boilinG pointSGet Full Solutions
The increase in energy associated with a bond angle that has deviated from the preferred angle of 109.5°.
Energetic electrons emitted from the nucleus, symbol 0-1e or b-. (Section 21.1)
A substance capable of accepting a proton. (4.3)
An apparatus that measures the heat released or absorbed in a chemical or physical process. (Section 5.5)
Polyhydroxy aldehydes or ketones with molecular formula CxH2xOx.
Properties that describe a substance’s composition and its reactivity; how the substance reacts or changes into other substances. (Section 1.3)
A triplet of nucleotides on mRNA that directs incorporation of a specifi c amino acid into a polypeptide sequence.
colloids (colloidal dispersions)
Mixtures containing particles larger than normal solutes but small enough to remain suspended in the dispersing medium. (Section 13.6)
The species formed when a base accepts a proton from an acid
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)
Atoms or groups on an atom that are bonded to an atom that is bonded to two nonidentical groups, one of which contains a chiral center. When one of the atoms or groups is replaced by another group, a new chiral center is created and a set of diastereomers results. The hydrogens of the CH2 group of 2-butanol, for example, are diastereotopic. Diastereotopic groups have different chemical shifts under all conditions
A carbohydrate containing two monosaccharide units joined by a glycosidic bond.
A compound containing a halogen atom and a hydroxyl group on adjacent carbons; those containing Br and OH are bromohydrins, and those containing Cl and OH are chlorohydrins.
A reaction in which an amino group is treated with excess methyl iodide, thereby converting it into an excellent leaving group, followed by treatment with a strong base to give an E2 reaction that yields an alkene.
Isoelectric point (pI)
The pH at which an amino acid, polypeptide, or protein has no net charge
the number of degrees through which a compound rotates the plane of polarized light
A ligand in which two or more donor atoms can coordinate to the same metal ion. (Section 23.3)
A biopolymer formed from amino acids. (Section 24.7)
A polymer, comprised of more than one kind of repeating unit, in which there is a random distribution of repeating units.
A step-by-step description of how a chemical reaction occurs.