- Chapter 1:
- Chapter 10:
- Chapter 11:
- Chapter 12:
- Chapter 13:
- Chapter 14:
- Chapter 15:
- Chapter 16:
- Chapter 17:
- Chapter 18:
- Chapter 19:
- Chapter 2:
- Chapter 20:
- Chapter 21:
- Chapter 22:
- Chapter 23:
- Chapter 24:
- Chapter 25:
- Chapter 26:
- Chapter 27:
- Chapter 28:
- Chapter 3:
- Chapter 4:
- Chapter 5:
- Chapter 6:
- Chapter 7:
- Chapter 8:
- Chapter 9:
General Chemistry: Principles and Modern Applications 10th Edition - Solutions by Chapter
Full solutions for General Chemistry: Principles and Modern Applications | 10th Edition
General Chemistry: Principles and Modern Applications | 10th Edition - Solutions by ChapterGet Full Solutions
Carbohydrates that differ in confi guration only at their anomeric carbons.
Hydrocarbon compounds that contain a planar, cyclic arrangement of carbon atoms linked by both s and delocalized p bonds. (Section 24.2)
The distance between the centers of two bonded atoms. (Section 8.3)
A substance capable of donating a proton. (4.3)
A compound that delivers the elements of a carbene without actually producing a free carbene.
Properties of solutions that depend on the number of solute particles in solution and not on the nature of the solute particles. (12.6)
conservation of orbital symmetry
During a reaction, the requirement that the phases of the frontier MOs must be aligned.
critical temperature (Tc).
The temperature above which a gas will not liquefy. (11.8)
An ionic compound that is formed upon treatment of a primary amine with NaNO2 and HCl.
The process of preparing a less concentrated solution from a more concentrated one by adding solvent. (Section 4.5)
free induction decay
In NMR spectroscopy, a complex signal which is a combination of all of the electrical impulses generated by each type of proton.
A spectrum that contains radiation at only certain specific wavelengths. (Section 6.3)
Light for which all photons have the same polarization, generally formed by passing light through a polarizing filter.
rare earth element
See lanthanide element. (Sections 6.8 and 6.9)
A conformational change in which one chair conformation is converted into the other.
A unimolecular nucleophilic substitution reaction.
sp2 Hybrid orbital
A hybrid atomic orbital formed by the combination of one s atomic orbital and two 2p atomic orbitals.
For a chiral compound that is subjected to plane-polarized light, the observed rotation when a standard concentration (1 g/mL) and a standard path length (1 dm) are used.
A double-helix model for the secondary structure of a DNA molecule
The distance between adjacent peaks of an oscillating magnetic or electric field.