- Chapter 1: Covalent Bonding and Shapes of Molecules
- Chapter 10: Alcohols
- Chapter 11: Ethers, Epoxides, and Sulfides
- Chapter 12: Infrared Spectroscopy
- Chapter 13: Nuclear Magnetic Resonance Spectroscopy
- Chapter 14: Mass Spectrometry
- Chapter 15: An Introduction to Organometallic Compounds
- Chapter 16: Aldehydes and Ketones
- Chapter 17: Carboxylic Acids
- Chapter 18: Functional Derivatives of Carboxylic Acids
- Chapter 19: Enolate Anions and Enamines
- Chapter 2: Constitutional Isomerism in Alkanes
- Chapter 20: Dienes, Conjugated Systems, and Pericyclic Reactions
- Chapter 21: Benzene and the Concept of Aromaticity
- Chapter 22: Reactions of Benzene and Its Derivatives
- Chapter 23: Amines
- Chapter 24: Catalytic Carbon-Carbon Bond Formation
- Chapter 3: Stereoisomerism and Chirality
- Chapter 4: Acids and Bases
- Chapter 5: Structure of Alkenes
- Chapter 6: Electrophilic Additions
- Chapter 7: Alkynes
- Chapter 8: Haloalkanes, Halogenation, and Radical Reactions
- Chapter 9: Nucleophilic Substitution and b-Elimination
Organic Chemistry 7th Edition - Solutions by Chapter
Full solutions for Organic Chemistry | 7th Edition
A reaction in which bonds are broken in the presence of an acid. For example, in the presence of a strong acid, an ether is converted into two alkyl halides.
The enthalpy change, ?H, required to break a particular bond when the substance is in the gas phase. (Section 8.8)
An atom or group of atoms bearing a positive charge.
The species formed when a base accepts a proton from an acid
Compounds containing the CN2 ion. (22.3)
In bond-line structures, agroup going behind the page.
Stereoisomers that are not mirror images of one another.
The process of separating compounds on the basis of their electric charge
The point in a titration at which the added solute reacts completely with the solute present in the solution. (Section 4.6)
A twodimensional representation of a molecule; in these projections, groups on the right and left are by convention in front, while those at the top and bottom are to the rear.
gas constant (R)
The constant of proportionality in the ideal-gas equation. (Section 10.4)
hydrogen deficiency index (HDI)
A measure of the number of degrees of unsaturation in a compound.
Molecules with low molecular weights, which can be joined together (polymerized) to form a polymer. (Section 12.8)
A reagent used for allylic bromination to avoid a competing reaction in which bromine adds across the p bond.
The special name given to the amide bond formed between the a-amino group of one amino acid and the a-carboxyl group of another amino acid
polar aprotic solvent
A solvent that lacks hydrogen atoms connected directly to an electronegative atom.
The energy that can be released if given an opportunity
The sloweststep in a multistep reaction which determines the rate of the reaction.
A process by which one or more compounds are removed from a mixture of organic compounds, based on a difference in solubility and/or acid-base properties.
Transfer RNA (tRNA
A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes
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