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Solutions for Chapter 5: Nomenclature

Full solutions for Introductory Chemistry: A Foundation | 7th Edition

ISBN: 9781439049402

Solutions for Chapter 5: Nomenclature

Solutions for Chapter 5
4 5 0 408 Reviews
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Textbook: Introductory Chemistry: A Foundation
Edition: 7
Author: Steven S. Zumdahl, Donald J. DeCoste
ISBN: 9781439049402

Chapter 5: Nomenclature includes 93 full step-by-step solutions. Since 93 problems in chapter 5: Nomenclature have been answered, more than 24199 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Introductory Chemistry: A Foundation, edition: 7. This expansive textbook survival guide covers the following chapters and their solutions. Introductory Chemistry: A Foundation was written by and is associated to the ISBN: 9781439049402.

Key Chemistry Terms and definitions covered in this textbook
  • Anomeric carbon

    The hemiacetal or acetal carbon of the cyclic form of a carbohydrate

  • bond enthalpy.

    The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)

  • Brønsted–Lowry acid

    A substance (molecule or ion) that acts as a proton donor. (Section 16.2)

  • Carbanion

    An ion in which carbon has an unshared pair of electrons and bears a negative charge.

  • Carbonyl group (Section 1.3C)

    A C"O group.

  • dilution

    The process of preparing a less concentrated solution from a more concentrated one by adding solvent. (Section 4.5)

  • Enthalpy change, DH

    The difference in total bond strengths and solvation between various points under comparison on a reaction coordinate diagram

  • equilibrium

    For a reaction, a state in which there is no longer an observable change in the concentrations of reactants and products.

  • frontier orbital theory

    The analysis of a reaction using MO theory, where only the frontier orbitals (HOMO and LUMO) are considered.

  • Homolytic bond cleavage

    Cleavage of a bond so that each fragment retains one electron; formation of radicals.

  • hydrogen abstraction

    In radical reactions, a type of arrow-pushing pattern in which a hydrogen atom is abstracted by a radical, generating a new radical.

  • nomenclature

    A system for naming organic compounds.

  • Phospholipid

    A lipid containing glycerol esterifi ed with two molecules of fatty acid and one molecule of phosphoric acid.

  • positron emission

    A nuclear decay process where a positron, a particle with the same mass as an electron but with a positive charge, symbol 0+1e, or b+ is emitted from the nucleus. (Section 21.1)

  • Reactive intermediate

    A high-energy species formed between two successive reaction steps, that lies in an energy minimum between the two transition states

  • Resonance energy

    The difference in energy between a resonance hybrid and the most stable of its hypothetical contributing structures in which electrons are localized on particular atoms and in particular bonds.

  • soluble

    A term used to indicate that a certain volume of a compound will dissolve in a specified amount of a liquid at room temperature.

  • solvation

    The clustering of solvent molecules around a solute particle. (Section 13.1)

  • Terpene

    A compound whose carbon skeleton can be divided into two or more units identical with the carbon skeleton of isoprene

  • Z

    For alkenes, a stereodescriptor that indicates that the two priority groups are on the same side of the p bond.