- Chapter 1: Chemical Foundations
- Chapter 10: Liquids and Solids
- Chapter 11: Properties of Solutions
- Chapter 12: Chemical Kinetics
- Chapter 13: Chemical Equilibrium
- Chapter 14: Acids and Bases
- Chapter 15: Applications of Aqueous Equilibria
- Chapter 16: Spontaneity, Entropy, and Free Energy
- Chapter 17: Electrochemistry
- Chapter 18: The Nucleus: A Chemists View
- Chapter 19: The Representative Elements: Groups 1A Through 4A
- Chapter 2: Atoms, Molecules, and Ions
- Chapter 20: The Representative Elements: Groups 5A Through 8A
- Chapter 21: Transition Metals and Coordination Chemistry
- Chapter 22: Organic and Biological Molecules
- Chapter 3: Stoichiometry
- Chapter 4: Types of Chemical Reactions and Solution Stoichiometry
- Chapter 5: Gases
- Chapter 6: Thermochemistry
- Chapter 7: Atomic Structure and Periodicity
- Chapter 8: Bonding: General Concepts
- Chapter 9: Covalent Bonding: Orbitals
Chemistry 7th Edition - Solutions by Chapter
Full solutions for Chemistry | 7th Edition
A reaction that achieves the addition of water across a double bond in the presence of an acid catalyst.
Hormones that are secreted by the cortex (the outer layer) of the adrenal glands. Adrenocortical hormones are typically characterized by a carbonyl group or hydroxyl group at C11 of the steroid skeleton.
A radical reaction that achieves installation of a bromine atom at an allylic position.
Organic bases that have the functional group —NR2, where R may be H, an alkyl group, or an aromatic group. (24.4)
Benzyl group (C6H5CH2!)
The group derived from toluene by removing a hydrogen from its methyl group.
A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.
From the Greek, cheir meaning hand; an object that is not superposable on its mirror image; an object that has handedness.
A term describing a molecule or an ion that cannot be superimposed on its mirror image. (Sections 23.4 and 24.5)
A compound in which two p bonds are separated from each other by exactly one s bond.
A signal of an NMR spectrum that is shifted toward the left (larger chemical shift) on the chart paper.
The steric interaction that results when two groups in a Newman projection are separated by a dihedral angle of 60°.
Atoms of the same element containing different numbers of neutrons and therefore having different masses. (Section 2.3)
Numbers of protons and neutrons that result in very stable nuclei. (Section 21.2)
nematic liquid crystalline phase
A liquid crystal in which the molecules are aligned in the same general direction, along their long axes, but in which the ends of the molecules are not aligned. (Section 11.7)
A material that can be formed into particular shapes by application of heat and pressure. (Section 12.8)
For light, the orientation of the electric field.
A triglyceride having several carbon-carbon double bonds in the hydrocarbon chains of its three fatty acids.
Compounds containing a mercapto group (SH).
An excellent leaving group (OTs). transition state (Sect. 6.6): A state through which a reaction passes. On an energy diagram, a transition state corresponds with a local maximum.
The outermost occupied electron shell of an atom.