- Chapter 1: A Review of General Chemistry
- Chapter 10: Alkynes
- Chapter 11: Radical Reactions
- Chapter 12: Synthesis
- Chapter 13: Alcohols and Phenols
- Chapter 14: Ethers and Epoxides; Thiols and Sulfides
- Chapter 15: Infrared Spectroscopy and Mass Spectrometry
- Chapter 16: Nuclear Magnetic Resonance Spectroscopy
- Chapter 17: Conjugated Pi Systems and Pericyclic Reactions
- Chapter 18: Aromatic Compounds
- Chapter 19: Aromatic Substitution Reactions
- Chapter 2: Molecular Representations
- Chapter 20: Aldehydes and Ketones
- Chapter 21: Carboxylic Acids and Their Derivatives
- Chapter 22: Alpha Carbon Chemistry: Enols and Enolates
- Chapter 23: Amines
- Chapter 24: Carbohydrates
- Chapter 25: Amino Acids, Peptides, and Proteins
- Chapter 26: Lipids
- Chapter 27: Synthetic Polymers
- Chapter 3: Acids and Bases
- Chapter 4: Alkanes and Cycloalkanes
- Chapter 5: Stereoisomerism
- Chapter 6: Chemical Reactivity and Mechanisms
- Chapter 7: Substitution Reactions
- Chapter 8: Alkenes: Structure and Preparation via Elimination Reactions
- Chapter 9: Addition Reactions of Alkenes
Organic Chemistry, - Standalone Book 2nd Edition - Solutions by Chapter
Full solutions for Organic Chemistry, - Standalone Book | 2nd Edition
Element in which the 5f orbitals are only partially occupied. (Section 6.8)
Polymers that are formed via cationic addition, anionic addition, or free-radical addition.
A reaction in which two atoms or groups of atoms react with a double bond, forming a compound with the two new groups bonded to the carbons of the original double bond.
A dicarboxylic acid that is produced when an aldose or ketose is treated with a strong oxidizing agent, such as HNO3.
A reaction that achieves the installation of an alkyl group. For example, an SN2 reaction in which an alkyl group is connected to an attacking nucleophile.
alpha (a) rays.
Helium ions with a positive charge of 12. (2.2)
atomic mass unit (amu)
A unit of measure equivalent to 1 g divided by Avogadro’s number.
In a bicyclic system, the carbon atoms where the rings are fused together.
A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).
concentration of a solution.
The amount of solute present in a given quantity of solvent or solution. (4.5)
Protein that does not exhibit normal biological activities. (25.3)
The group that is formed when two cysteine residues of a polypeptide or protein are joined together.
The charge on an atom in a polyatomic ion or molecule
Ionization potential (IP)
The minimum energy required to remove an electron from an atom or molecule to a distance where there is no electrostatic interaction between the resulting ion and electron.
A device that uses strong magnetic and electrostatic fields to accelerate charged particles. (Section 21.3)
A macromolecule containing many amino acid units, each joined to the next by a peptide bond
The energy that can be released if given an opportunity
ribonucleic acid (RNA)
A polynucleotide in which ribose is the sugar component. (Section 24.10)
A bimolecular nucleophilic substitution reaction.
A conformation in which nearby groups in a Newman projection have a dihedral angle of 60°.