- 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
An organic compound that contains a carbonyl group 1C “O2 to which at least one hydrogen atom is attached. (Section 24.4)
Compounds containing a carbon-carbon triple bond.
A high-energy molecular orbital resulting from the destructive interference between atomic orbitals.
buffered solution (buffer)
A solution that undergoes a limited change in pH upon addition of a small amount of acid or base. (Section 17.2)
A complex polymer resulting from the polymerization of two or more chemically different monomers. (Section 12.8)
A solid that possesses rigid and long-range order; its atoms, molecules, or ions occupy specific positions. (11.4)
Incorporation of a hetero atom into a solid to change its electrical properties. For example, incorporation of P into Si. (Section 12.7)
A reaction involving the loss of a leaving group and formation of a p bond.
A reaction that involves the addition of X2 (either Br2 or Cl2) across an alkene.
Members of group 7A in the periodic table. (Section 7.8)
A nonpolar group that does not have favorable interactions with water.
The sum of the number of protons and neutrons in the nucleus of a particular atom. (Section 2.3)
The concentration of a solution expressed as moles of solute per liter of solution; abbreviated M. (Section 4.5)
A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.
A mixture of equal amounts of two enantiomers.
The manner in which a protein is coiled or stretched. (Section 24.7)
In NMR spectroscopy,protons or carbon atoms whose surrounding electron density is rich.
Atomic orbitals that are achieved by mathematically averaging one s orbital with two p orbitals to form three hybridized atomic orbitals.
A name that is assigned using the rules of IUPAC nomenclature.
tertiary alkyl halide
An organohalide in which the alpha (a) position is connected to three alkyl groups.
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