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Solutions for Chapter 11.3: Gas Volumes andthe Ideal Gas Law
Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition
The product obtainedfrom 1,2-addition across a conjugated p system.
The process of introducing an acyl group, RCO! or ArCO!, onto an organic molecule.
A common non-SI unit of length, denoted Å, that is used to measure atomic dimensions: 1Å = 10-10 m. (Section 2.3)
An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.
A polydentate ligand that is capable of occupying two or more sites in the coordination sphere. (Section 23.3)
Compounds or ions that are not superimposable with their mirror images. (23.4)
The intermolecular attraction between like molecules. (11.3)
A polymer in which neighboring chains are linked together, for example, by disulfide bonds.
A cyclohexene resulting from the cycloaddition reaction of a diene and a dienophile.
A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)
Triglycerides that are solids atroom temperature.
An orbital formed by the combination of two or more atomic orbitals.
A reaction in which a proton and a hydroxyl group (OH) are added across a p bond.
Compounds composed of only carbon and hydrogen. (Section 2.9)
One that occurs at constant temperature. (Section 19.1)
The energy that an object possesses by virtue of its motion. (Section 5.1)
A CH2 group.
The product formed when a nucleoside is coupled to a phosphate group
A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A clockwise sequence for 1-2-3 is designated as R.
A signal of an NMR spectrum that is shifted toward the right (smaller chemical shift) on the chart paper.
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