- 1.12SE.1PE: Converting Volume UnitsEarth's oceans contain approximately 1.36 * ...
- 1.12SE.2PE: Converting Volume UnitsEarth's oceans contain approximately 1.36 * ...
Solutions for Chapter 1.12SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
A compound that has the general formula R3N, where R may be H or a hydrocarbon group. (Section 16.7)
A conformation in which the dihedral angle between two groups is 180°.
An amine in which nitrogen is bonded to one or more aryl groups.
In IR spectroscopy, when two bonds are stretching out of phase with each other.
An ion in which carbon has an unshared pair of electrons and bears a negative charge.
A microcrystalline form of carbon. (Section 22.9)
Carboxyl group (Section 1.3D)
A !COOH group.
Atoms or groups on an atom that are bonded to an atom that is bonded to two nonidentical groups, one of which contains a chiral center. When one of the atoms or groups is replaced by another group, a new chiral center is created and a set of diastereomers results. The hydrogens of the CH2 group of 2-butanol, for example, are diastereotopic. Diastereotopic groups have different chemical shifts under all conditions
An anion derived by loss of a hydrogen from a carbon alpha to a carbonyl group; the anion of an enol.
A fi ve-membered cyclic form of a monosaccharide.
A conformation that exhibits a gauche interaction.
Cleavage of a single bond by H2, most commonly accomplished by treating a compound with H2 in the presence of a transition metal catalyst.
A measure of the strength of an acid: Ka = Keq 3H2O4 = 3H3O+ 4 3A- 4 3HA4
The main fabricof cell membranes, assembled primarily fromphosphoglycerides.
Molar absorptivity (e)
The absorbance of a 1 M solution of a compound.
A region of space that can hold two electrons
Polypeptide chains comprised of more than 40 or 50 amino acids.
Rate determining step
The step in a multistep reaction sequence that crosses the highest energy barrier.
Secondary structure of nucleic acids
The ordered arrangement of nucleic acid strands
A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.