- 7.2.6: Name the following: a. CH2 CHCH2C CCH2CH3 d. HOCH2CH2C CH b. CH3CH ...
- 7.2.7: Name the following:
Solutions for Chapter 7.2: How to Name a Compound That Has More than One Functional Group
Full solutions for Organic Chemistry | 7th Edition
Solutions for Chapter 7.2: How to Name a Compound That Has More than One Functional GroupGet Full Solutions
The conjugate base of acetylene or any terminal alkyne.
Lacking a sugar
A group that is formed by removing a hydrogen atom from an alkane. (Section 25.3)
Male sex hormones.
Enantiomers that lack a chiral center and differ because of hindered rotation.
An electrophilic aromatic substitution reaction in which an aryldiazonium salt reacts with an activated aromatic ring.
An ion in which carbon has an unshared pair of electrons and bears a negative charge.
A microcrystalline form of carbon. (Section 22.9)
Cis, trans isomers
Stereoisomers that have the same connectivity but a different arrangement of their atoms in space as a result of the presence of either a ring or a carboncarbon double bond.
A reaction in which a carbonyl group is completely reduced and replaced with two hydrogen atoms.
A dispersion of particles of one substance (the dispersed phase) throughout a dispersing medium made of another substance. (12.8)
The mass of the collection of atoms represented by a chemical formula. For example, the formula weight of NO2 (46.0 amu) is the sum of the masses of one nitrogen atom and two oxygen atoms. (Section 3.3)
gas constant (R)
The constant of proportionality in the ideal-gas equation. (Section 10.4)
heat of vaporization
The enthalpy change, ?H, for vaporization of a liquid. (Section 11.4)
In radical reaction mechanisms, a step in which radicals are created.
A bond between oppositely charged ions. The ions are formed from atoms by transfer of one or more electrons. (Section 8.1)
A set of assumptions about the nature of gases. These assumptions, when translated into mathematical form, yield the ideal-gas equation. (Section 10.7)
A polymer chain that continues to grow without chain-termination steps until either all of the monomer is consumed or some external agent is added to terminate the chain. The polymer chains will continue to grow if more monomer is added.
Groups that strongly activate an aromatic ring toward electrophilic aromatic substitution, thereby significantly enhancing the rate of the reaction.
An ether (R!O!R) where both R groups are identical.