- 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
Polyhydroxy aldehydes or ketones with molecular formula CxH2xOx.
conservation of orbital symmetry
During a reaction, the requirement that the phases of the frontier MOs must be aligned.
The process by which a metal is oxidized by substances in its environment. (Section 20.8)
crossed aldol reaction
An aldol reaction that occurs between different partners.
crystalline solid (crystal)
A solid whose internal arrangement of atoms, molecules, or ions possesses a regularly repeating pattern in any direction through the solid. (Section 12.2)
The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.
A procedure for preparing a less concentrated solution from a more concentrated solution. (4.5)
A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)
A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.
A compound containing an oxygen atom bonded to two carbon atoms.
Strands of a polymer that are generated when the polymer is heated, forced through small holes, and then cooled.
A drawing style that is often used when dealing with compounds bearing multiple chirality centers, especially for carbohydrates. (See also Sect. 5.7.)
free induction decay
In NMR spectroscopy, a complex signal which is a combination of all of the electrical impulses generated by each type of proton.
Solids that are composed of metal atoms. (Section 12.1)
A compound that consists of molecules. (Section 2.6)
Replacing this hydrogen by deuterium gives a chiral center with an R confi guration
A solvent that is a hydrogen-bond donor. Common protic solvents are water, low-molecular-weight alcohols, and low-molecular weight carboxylic acids.
renewable energy sources
Energy such as solar energy, wind energy, and hydroelectric energy derived from essentially inexhaustible sources. (Section 5.8)
The manner in which a protein is coiled or stretched. (Section 24.7)
A unimolecular nucleophilic substitution reaction.