- 22.2.1: List the basic structural features that characterize each of the fo...
- 22.2.2: Draw all of the condensed structural formulas that can represent C5...
- 22.2.3: Give the systematic name for each compound in your answers to item 2.
- 22.2.4: Give examples of a property or use of three hydrocarbons.
- 22.2.5: Name the following compounds: a. CH3- CH2 _ -CH3 CH3 - CH- CH- CH2-...
- 22.2.6: ANALYZING INFORMATION Write the structural formulas for an alkane, ...
Solutions for Chapter 22.2: Hydrocarbons
Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition
A substance that is able to donate a H+ ion (a proton) and, hence, increases the concentration of H+1aq2 when it dissolves in water. (Section 4.3)
Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)
A substituent lacking p bonds and comprised of only carbon and hydrogen atoms.
In a crystal lattice it is defined as the number of atoms (or ions) surrounding an atom (or ion) (11.4). In coordination compounds it is defined as the number of donor atoms surrounding the central metal atom in a complex. (23.3)
A lone pair or charge that is participating in resonance.
Stereoisomers that are nonsuperposable mirror images of each other; refers to a relationship between pairs of objects
A process in which a carboxylic acid is converted into an ester when treated with an alcohol in the presence of an acid catalyst.
A simple method for drawing the relative energy levels of the MOs for a ring assembled from continuously overlapping p orbitals.
A vacancy in the valence band of a semiconductor, created by doping. (Section 12.7)
A type of carbocation rearrangement that involves the migration of a hydride ion (H-).
One that occurs at constant temperature. (Section 19.1)
A group of molecules arranged in a sphere such that the surface of the sphere is comprised of polar groups, rendering the micelle water soluble.
A combination of two or more substances in which each substance retains its own chemical identity. (Section 1.2)
the number of degrees through which a compound rotates the plane of polarized light
A conformation in which a hydrogen atom and a leaving group are approximately coplanar.
Reversibly creating an unreactive group for the purpose of preventing a functional group from potentially reacting to give an unwanted product or products
S (Section 3.3
From the Latin, sinister, left; used in the R,S convention to show that the order of priority of groups on a chiral center is counterclockwise
sigma 1S2 bond
A covalent bond in which electron density is concentrated along the internuclear axis. (Section 9.6)
A unimolecular nucleophilic substitution reaction.
A reaction in which one substrate produces two stereoisomers in unequal amounts.