- 10.3.10.7: Rank the C H bonds of trans-3-hexene in order of decreasing bond di...
- 10.3.10.8: Assume that N-bromosuccinimide serves as a source of Br2, and write...
- 10.3.10.9: Evaluate 2,3,3-trimethyl-1-butene as a candidate for free-radical b...
Solutions for Chapter 10.3: Allylic Free-Radical Halogenation
Full solutions for Organic Chemistry, | 9th Edition
A liquid mixture of constant composition with a boiling point that is different from that of any of its components.
An instrument that measures atmospheric pressure. (5.2)
A substance capable of accepting a proton. (4.3)
A binary compound of carbon with a metal or metalloid. (Section 22.9)
Processes in which one or more substances are converted into other substances; also called chemical reactions. (Section 1.3)
A technique by which compounds are separated from each other based on a difference in the way they interact with the medium (the adsorbent) through which they are passed.
complete ionic equation
A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)
The spreading of a charge or lone pair as described by resonance theory.
Refers to the steric strain arising from interaction between an axial substituent and an axial hydrogen (or other group) on the same side of a chair conformation of a cyclohexane ring
See voltaic cell. (Section 20.3)
A form of isomerism in which compounds with the same type and number of atoms and the same chemical bonds have different spatial arrangements of these atoms and bonds. (Sections 23.4 and 24.4)
heat of vaporization
The enthalpy change, ?H, for vaporization of a liquid. (Section 11.4)
A vacancy in the valence band of a semiconductor, created by doping. (Section 12.7)
A compound capable offunctioning as an electron pair acceptor.
From the Greek, mono 1 meros, meaning single part. The simplest nonredundant unit from which a polymer is synthesized.
An intermediate with a positively charged oxygen atom.
rare earth element
See lanthanide element. (Sections 6.8 and 6.9)
A term used to indicate that a certain volume of a compound will dissolve in a specified amount of a liquid at room temperature.
A reaction for which the ratio of products is determined solely by the distribution of energy among the products.
In bond-line structures, a group in front of the page.