- 17.8SE.1PE: Calculations for a Weak Acid-Strong Base TitrationCalculate the pH ...
- 17.8SE.2PE: Calculations for a Weak Acid-Strong Base TitrationCalculate the pH ...
Solutions for Chapter 17.8SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
A carbon atom adjacent to a carbonyl group
A compound that contains both an amino group and a carboxyl group
In UV-Vis spectroscopy, an equation describing the relationship between molar absorptivity (e), absorbance (A), concentration (C), and path length (l): e = A (C Ž l)
A binary compound of carbon with a metal or metalloid. (Section 22.9)
The generally larger formation constants for polydentate ligands as compared with the corresponding monodentate ligands. (Section 23.3)
continuous-wave (CW) spectrometer
An NMR spectrometer that holds the magnetic field constant and slowly sweeps through a range of rf frequencies, monitoring which frequencies are absorbed.
The separation on an NMR spectrum (in hertz) between adjacent peaks in a multiplet and a quantitative measure of the infl uence of the spin-spin coupling with adjacent nuclei.
A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.
A form of magnetism in which unpaired electron spins align parallel to one another. (Section 23.1)
The SI unit for radiation dose
A compound containing an !OOH group.
Compounds formed between two different halogen elements. Examples include IBr and BrF3. (Section 22.4)
A system for naming organic compounds.
Having no net overlap.
Plane of symmetry
An imaginary plane passing through an object dividing it so that one half is the mirror image of the other half
polar aprotic solvent
A solvent that lacks hydrogen atoms connected directly to an electronegative atom.
Lipids that contain 20 carbon atoms and are characterized by a five-membered ring with two side chains.
A term describing a consideration that must be taken into account for a reaction in which two or more constitutional isomers can be formed.
A plant or animal lipid having the characteristic tetracyclic ring structure of the steroid nucleus, namely three sixmembered rings and one fi ve-membered ring.
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.