- 3.5SE.1PE: Calculating Formula Weights Calculate the formula weight of (a) suc...
- 3.5SE.2PE: Calculating Formula Weights Calculate the formula weight of (a) suc...
Solutions for Chapter 3.5SE: Chemistry: A Molecular Approach 3rd Edition
Full solutions for Chemistry: A Molecular Approach | 3rd Edition
In IR spectroscopy as well as UV-VIS spectroscopy, a plot that measures the percent transmittance or absorption as a function of frequency.
The conjugate base of acetylene or any terminal alkyne.
Carbohydrates that differ in confi guration only at their anomeric carbons.
In mass spectrometry, the tallest peak in the spectrum, which is assigned a relative value of 100%.
A semiconducting material formed from two or more elements. (Section 12.7)
degree of substitution
For alkenes, a classification method that refers to the number of alkyl groups connected to the double bond.
An eliminationreaction in which the leaving group only leavesafter deprotonation occurs. This process occurs atthe end of an aldol condensation.
Enantiomeric excess (ee)
The difference between the percentage of two enantiomers in a mixture
A conformation that exhibits a gauche interaction.
Ground-state electron confi guration
The lowest-energy electron confi guration for an atom or molecule.
Compounds formed when hydrogen reacts with alkali metals and also the heavier alkaline earths (Ca, Sr, and Ba); these compounds contain the hydride ion, H-. (Section 22.2)
The energy required to remove an electron from a gaseous atom when the atom is in its ground state. (Section 7.4)
A pair of unshared, or nonbonding, electrons.
The very small, very dense, positively charged portion of an atom; it is composed of protons and neutrons. (Section 2.2)
A compound that contains an !OH bonded to a benzene ring; a benzenol.
Light oscillating in only parallel planes.
A polymer constructed from nucleotides linked together.
A molecule, ion, or radical described as a composite of a number of contributing structures
Atomic orbitals that are achieved by mathematically averaging one s orbital with two p orbitals to form three hybridized atomic orbitals.
A nonplanar conformation of a cyclohexane ring that is twisted from and slightly more stable than a boat conformation.