- 126.96.36.199: Draw a Lewis structure for each of the following alkynes. (a) isopr...
- 188.8.131.52: Provide the substitutive name for each of the following compounds. ...
Solutions for Chapter 14.2: nomenclature of alkyneS
Full solutions for Organic Chemistry | 6th Edition
A list of metals in order of decreasing ease of oxidation. (Section 4.4)
A hydrocarbon that lacks p bonds.
Any reaction in which an atom or group of atoms is substituted for another atom or group of atoms at an allylic carbon.
alpha 1A2 helix
A protein structure in which the protein is coiled in the form of a helix with hydrogen bonds between C “O and N ¬H groups on adjacent turns. (Section 24.7)
Carbohydrates that differ in confi guration only at their anomeric carbons.
Any property of a substance that cannot be studied without converting the substance into some other substance. (1.6)
A compound inwhich two carbon-carbon p bonds are separated from each other by exactly one s bond.
An effect that causes different regions of space to be characterized by different magnetic field strengths.
Very weak intermolecular forces of attraction resulting from the interaction between temporary induced dipoles
Polymers that return to their original shape after being stretched.
Measures chaos versus order and chaos is favorable
Any process with a negative DH (the system gives energy to the surroundings).
A compound containing a carbon-nitrogen double bond, R2C"NR’; also called a Schiff base
The force that exists between an ion and a neutral polar molecule that possesses a permanent dipole moment. (Section 11.2)
A carbohydrate that cannot be hydrolyzed to a simpler carbohydrate.
An organic compound containing at least one halogen.
A chain comprised of a small number of amino acid residues.
A process in which heat converts a mineral in an ore from one chemical form to another and eventually to the free metal. (Section 23.2)
A method that chemists use to deal with the inadequacy of bond-line drawings.
A list of ligands arranged in order of their abilities to split the d-orbital energies (using the terminology of the crystal-field model). (Section 23.6)