- 9.9SE.1PE: Molecular Orbitals of a Period 2 Diatomic IonFor the 02+ ion predic...
- 9.9SE.2PE: Molecular Orbitals of a Period 2 Diatomic IonFor the 02+ ion predic...
Solutions for Chapter 9.9SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
activated complex (transition state)
The particular arrangement of atoms found at the top of the potential-energy barrier as a reaction proceeds from reactants to products. (Section 14.5)
The species temporarily formed by the reactant molecules as a result of the collision before they form the product. (13.4)
An SR group.
An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.
A molecule containing an !OH group and a !CN group bonded to the same carbon.
Refers to a substance that rotates the plane of polarized light to the right
dextrorotatory, or merely dextro or d
A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the right (clockwise). (Section 23.4)
A procedure for preparing a less concentrated solution from a more concentrated solution. (4.5)
A covalent bond involving two electron pairs. (Section 8.3)
In radical reactions, a type of arrow-pushing pattern in which a halogen atom is abstracted by a radical, generating a new radical.
A way to view furanose and pyranose forms of monosaccharides. The ring is drawn fl at and most commonly viewed through its edge with the anomeric carbon on the right and the oxygen atom of the ring to the rear
A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.
Le Châtelier’s principle
A principle stating that when we disturb a system at chemical equilibrium, the relative concentrations of reactants and
levorotatory, or merely levo or l
A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the left (counterclockwise). (Section 24.4)
A variety of enzymes that selectively hydrolyze specific peptide bonds.
Changes (such as a phase change) that occur with no change in chemical composition. (Section 1.3)
A macromolecule containing many amino acid units, each joined to the next by a peptide bond
polyvinyl chloride, (PVC)
A polymer formed from the polymerization of vinyl chloride (H2CRCHCl).
A polymerization in which chain growth occurs in a stepwise manner between difunctional monomers as, for example, between adipic acid and hexamethylenediamine to form nylon 66. Also called condensation polymerization.
Stork enamine synthesis
A Michaelreaction in which an enamine functions as anucleophile.