Organic Chemistry 6th Edition - Solutions by Chapter

A basic nitrogen-containing compound of plant origin, many of which are physiologically active when administered to humans.

Hydrocarbons containing one or more carbon–carbon triple bonds. (Section 24.2)

The C1 position of the cyclic hemiacetal of an aldose or the C2 position of the cyclic hemiacetal of a ketose.

A term used to classify benzene and its derivatives.

Enantiomers that lack a chiral center and differ because of hindered rotation.

A compound that can serve as a proton donor.

The process by which a liquid rises in a tube because of a combination of adhesion to the walls of the tube and cohesion between liquid particles. (Section 11.3)

Processes in which one or more substances are converted into other substances; also called chemical reactions. (Section 1.3)

A lipid that readily undergoes hydrolysis in aqueous acid or base to produce smaller fragments.

An acid and its conjugate base or a base and its conjugate acid. (15.1)

A substance formed by the loss of a proton from a Brønsted–Lowry acid. (Section 16.2)

A compound containing two hydroxyl groups

A class of lipids which includes leukotrienes, prostaglandins, thromboxanes, and prostacyclins.

The arrangement of electrons in the orbitals of an atom or molecule (Section 6.8)

The arrangement of electrons in an atom or molecule. (Chapter 6:Introduction)

A term in the Arrhenius equation that is related to the frequency of collision and the probability that the collisions are favorably oriented for reaction. (Section 14.5)

The reaction rate at a particular time as opposed to the average rate over an interval of time. (Section 14.2)

The temperature at which the crystallineregions of a polymer become amorphous.

The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.

Reactions in which one group is replaced by another group.