- 17.15.48: What is the product of each of the following reactions? a. CF3COO O...
- 17.15.49: a. What two sets of reagents (each consisting of a carbonyl compoun...
Solutions for Chapter 17.15: THE REACTIONS OF ALDEHYDES AND KETONES WITH A PEROXYACID
Full solutions for Organic Chemistry | 7th Edition
Solutions for Chapter 17.15: THE REACTIONS OF ALDEHYDES AND KETONES WITH A PEROXYACIDGet Full Solutions
A common non-SI unit of length, denoted Å, that is used to measure atomic dimensions: 1Å = 10-10 m. (Section 2.3)
A solution in which water is the solvent. (Chapter 4: Introduction)
An estimate of the size of an atom. See bonding atomic radius. (Section 7.3)
A nuclear decay process where a beta particle is emitted from the nucleus; also called beta decay. (Section 21.1)
A ligand in which two linked coordinating atoms are bound to a metal. (Section 23.3)
The most efficient arrangements for packing atoms, molecules, or ions in a crystal. (11.4)
When signal splitting occurs in NMR spectroscopy, the distance between the individual peaks of a signal.
A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.
The region of an IR spectrum that contains signals that arise from double bonds, triple bonds, and X!H bonds.
A simple method for drawing the relative energy levels of the MOs for a ring assembled from continuously overlapping p orbitals.
One that occurs at constant temperature. (Section 19.1)
The SI unit of energy, 1 kg@m2 >s2. A related unit is the calorie: 4.184 J = 1 cal. (Section 5.1)
Refers to a substance that rotates the plane of polarized light to the left.
Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)
The product of the mass, m, and velocity, v, of an object. (Section 6.4)
nuclear disintegration series
A series of nuclear reactions that begins with an unstable nucleus and terminates with a stable one; also called a radioactive series. (Section 21.2)
In NMR spectroscopy, a technique in which only the one-bond couplings are observed. CH3 groups appear as quartets, CH2 groups appear as triplets, CH groups appear as doublets, and quaternary carbon atoms appear as singlets.
On an aromatic ring, the C4position.
A covalent bond involving one electron pair. (Section 8.3)
Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.