- Lesson 55.1: Explain why hot air rises.
- Lesson 55.2: Explain the difference between a warm front and a cold front.
- Lesson 55.3: Suppose you have two gas samples in fl exible containers with the s...
- Lesson 55.4: A cold front is approaching your hometown and is due to arrive tomo...
- Lesson 55.5: A warm front is approaching your hometown and is due to arrive tomo...
- Lesson 55.6: The continental polar air mass overtakes the maritime tropical air ...
- Lesson 55.7: Look in the newspaper or on the Internet. Find a recent weather map...
Solutions for Chapter Lesson 55: Density, Temperature, and Fronts
Full solutions for Living by Chemistry | 2nd Edition
The conjugate base of acetylene or any terminal alkyne.
The product formed when the C"O group of a monosaccharide is reduced to a CHOH group.
A hydrocarbon that lacks p bonds.
A solid whose molecular arrangement lacks the regularly repeating long- range pattern of a crystal. (Section 12.2)
The addition of atoms or groups of atoms to opposite faces of a carbon-carbon double bond.
A reactive intermediate formed by b-elimination from adjacent carbon atoms of a benzene ring and having a triple bond in the benzene ring. The second p bond of the benzyne triple bond is formed by the weak overlap of coplanar 2p orbitals on adjacent carbons.
beta (b) rays.
The pressure at which a gas at its critical temperature is converted to a liquid state. (Section 11.4)
A reaction involving the loss of a leaving group and formation of a p bond.
A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.
Any process with a negative DG.
A compound containing two carbon-carbon p bonds that are separated by two or more s bonds.
A cyclic ester.
A reaction in which a nucleophile attacks a conjugated p system, resulting in a 1,4-addition.
plane of symmetry
A plane that bisects a compound into two halves that are mirror images of each other.
A molecule that possesses a nonzero dipole moment. (Section 8.4)
Possessing radioactivity, the spontaneous disintegration of an unstable atomic nucleus with accompanying emission of radiation. (Section 2.2; Chapter 21: Introduction)
The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.
The combination of a Michael addition followed by an aldol condensation to form a ring.
sp3 Hybrid orbital
A hybrid atomic orbital formed by the combination of one s atomic orbital and three 2p atomic orbitals.