- 3.7SE.1PE: Estimating Numbers of AtomsWithout using a calculator, arrange thes...
- 3.7SE.2PE: Estimating Numbers of AtomsWithout using a calculator, arrange thes...
Solutions for Chapter 3.7SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)
A !CH2CH"CH2 group.
An atom or group of atoms bearing a negative charge.
A polymer that is formed under conditions in which the monomers do not react directly with each other, but rather, each monomer is added to the growing chain, one at a time.
A technique by which compounds are separated from each other based on a difference in the way they interact with the medium (the adsorbent) through which they are passed.
Confi gurational isomers
Isomers that differ by the confi guration of substituents on an atom. Refers to the arrangement of atoms about a stereocenter
The electrons that are not in the outermost shell of an atom. (Section 6.8)
A material that, when stretched or otherwise distorted, returns to its original shape when the distorting force is released.
frontier orbital theory
The analysis of a reaction using MO theory, where only the frontier orbitals (HOMO and LUMO) are considered.
A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)
A metal complex in which the electrons are paired in lower-energy orbitals. (Section 23.6)
The removal of an electron from an atom or molecule by absorption of light. (Section 18.2)
The sequence of amino acids along a protein chain. (Section 24.7)
A polymer, comprised of more than one kind of repeating unit, in which there is a random distribution of repeating units.
Hydrolysis of an ester in the presence of a base. (Section 24.4)
A reaction that has a rate equation in which the sum of all exponents is two.
standard atmospheric pressure
Defined as 760 torr or, in SI units, 101.325 kPa. (Section 10.2)
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.
In radical reactions, a step in which two radicals are joined to give a compound with no unshared electrons.
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.