- 4.13.37: Which of the following compounds has a stereoisomer that is a meso ...
- 4.13.38: Which of the following are optically active? H3C CH3 H3C CH3 H3C CH...
- 4.13.39: Draw all the stereoisomers for each of the following: a. 1-bromo-2-...
Solutions for Chapter 4.13: Meso Compounds Have Asymmetric Centers but Are Optically Inactive
Full solutions for Organic Chemistry | 7th Edition
Solutions for Chapter 4.13: Meso Compounds Have Asymmetric Centers but Are Optically InactiveGet Full Solutions
The closeness of a measurement to the true value of the quantity that is measured. (1.8)
An SR group.
In IR spectroscopy, when two bonds are stretching out of phase with each other.
A reaction in which a substance reacts with oxygen, usually with the release of heat and light, to produce a flame. (4.4)
coupling (of radicals)
A radical process in which two radicals join together and form a bond.
A bond in which two electrons are shared by two atoms. (9.4)
A cyclic polyether derived from ethylene glycol and substituted ethylene glycols.
Having the same energy.
A collection of orbitals that have the same value of n. For example, the orbitals with n = 3 (the 3s, 3p, and 3d orbitals) comprise the third shell. (Section 6.5)
A catalyst that is in a different phase from that of the reactant substances. (Section 14.7)
A polymer in which the repeating units contain chirality centers which all have the same configuration.
Points in a crystal all of which have identical environments. (Section 12.2)
A pair of unshared, or nonbonding, electrons.
A device inwhich a compound is first vaporized and convertedinto ions, which are then separated anddetected.
Thedetermining factor by which ions are separatedfrom each other in mass spectrometry.
The pressure that must be applied to a solution to stop osmosis from pure solvent into the solution. (Section 13.5)
A cyclic ether containing a three-membered ring system. Also called an epoxide.
Resonance in NMR spectroscopy
The absorption of electromagnetic radiation by a precessing nucleus and the resulting “fl ip” of its nuclear spin from the lower energy state to the higher energy state.
A plant or animal lipid having the characteristic tetracyclic ring structure of the steroid nucleus, namely three sixmembered rings and one fi ve-membered ring.
A polymer that can be molded when it is fi rst prepared, but once cooled, hardens irreversibly and cannot be remelted.