- 188.8.131.52: Write structural formulas for all the constitutional isomers that h...
- 184.108.40.206: Nitrosomethane and formaldoxime both have the molecular formula CH3...
- 220.127.116.11: Expand the bond-line formulas of the amino acid cysteine and the ne...
Solutions for Chapter 1.7: Structural Formulas of Organic Molecules
Full solutions for Organic Chemistry, | 9th Edition
The number of protons in the nucleus of an atom of an element. (Section 2.3)
An elimination reaction in which a proton from the beta (b) position is removed together with the leaving group, forming a double bond.
An elementary reaction that involves two molecules. (Section 14.6)
The angles made by the lines joining the nuclei of the atoms in a molecule. (Section 9.1)
The distance between the centers of two bonded atoms. (Section 8.3)
A CRO bond. carboxylic acid derivative (Sect. 21.6): A compound that is similar in structure to a carboxylic acid (RCOOH) but the OH group of the carboxylic acid has been replaced with a different group, Z, where Z is a heteroatom such as Cl, O, N, etc. Nitriles (R!C#N) are also considered to be carboxylic acid derivatives because they have the same oxidation state as carboxylic acids.
The study of matter and the changes it undergoes. (1.1)
The intermolecular attraction between like molecules. (11.3)
Refers to the arrangement of atoms about a stereocenter
A reaction involving the loss of a leaving group and formation of a p bond.
The number of full cycles of a wave that pass a given point in a second, and reported in hertz (Hz), which has the units s21
A catalyst that is in a different phase from that of the reactant substances. (Section 14.7)
A polymer constructed from a single type of monomer.
A reaction that involves the addition of H and X (either Br or Cl) across an alkene.
A carbohydrate for which the chirality center farthest from the carbonyl group will have an OH group pointing to the left in the Fischer projection.
An abbreviated way to draw structural formulas in which vertices and line endings represent carbons
Compounds containing silicon and oxygen, structurally based on SiO4 tetrahedra. (Section 22.10)
In NMR spectroscopy, a signal that is comprised of only one peak.
Tertiary (3°) amine
An amine in which nitrogen is bonded to three carbons
Tertiary structure of nucleic acids
The threedimensional arrangement of all atoms of a nucleic acid, commonly referred to as supercoiling