- 18.104.22.168: Using models if necessary, draw at least two other line-and-wedge s...
- 22.214.171.124: Predict the approximate geometry in each of the following molecules.
- 126.96.36.199: Estimate each of the bond angles and order the bond lengths (smalle...
- 188.8.131.52: Which of the following ions require(s) dihedral angles to specify i...
Solutions for Chapter 1.3: Structures of Covalent Compounds
Full solutions for Organic Chemistry | 6th Edition
A compound containing a !CHO group
alpha (a) rays.
Helium ions with a positive charge of 12. (2.2)
The electrode at which oxidation occurs. (18.2)
antibonding molecular orbital.
A molecular orbital that is of higher energy and lower stability than the atomic orbitals from which it was formed. (10.6)
From the Greek, cheir meaning hand; an object that is not superposable on its mirror image; an object that has handedness.
delocalized molecular orbitals.
Molecular orbitals that are not confined between two adjacent bonding atoms but actually extend over three or more atoms. (10.8)
DEPT 13C NMR
In 13C NMR spectroscopy, a technique that utilizes two rf radiation emitters and provides information regarding the number of protons attached to each carbon atom in a compound.
In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)
A conformation about a single bond of an alkane in which two groups on adjacent carbons lie at a dihedral angle of 60°
Compounds that are similar in structure to CFCs but also possess at least one C!Hbond.
The withdrawal of electron density that occurs when a bond is shared by two atoms of differing electronegativity.
The product of the mass, m, and velocity, v, of an object. (Section 6.4)
An electrophilic aromatic substitution reaction that involves the installation of a nitro group (NO2) on an aromatic ring.
The common name for bicyclo[2.2.1]heptane.
A carbohydrate containing a large number of monosaccharide units, each joined to the next by one or more glycosidic bonds.
The slowest elementary step in a reaction mechanism. (Section 14.6)
A term used to describe the character of a chemical entity (molecule, ion, or radical) exhibiting more than one significant resonance structure.
The amount of time required for a compound to exit from a gas chromatograph.
A compound that contains no p bonds.
Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.