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Solutions for Chapter 19: CHEMICAL THERMODYNAMICS

Chemistry: The Central Science | 11th Edition | ISBN: 9780136006176 | Authors: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward

Full solutions for Chemistry: The Central Science | 11th Edition

ISBN: 9780136006176

Chemistry: The Central Science | 11th Edition | ISBN: 9780136006176 | Authors: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward

Solutions for Chapter 19: CHEMICAL THERMODYNAMICS

Solutions for Chapter 19
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Textbook: Chemistry: The Central Science
Edition: 11
Author: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward
ISBN: 9780136006176

Chapter 19: CHEMICAL THERMODYNAMICS includes 98 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science , edition: 11. Chemistry: The Central Science was written by and is associated to the ISBN: 9780136006176. Since 98 problems in chapter 19: CHEMICAL THERMODYNAMICS have been answered, more than 17314 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • 1,2-addition

    A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C2 position.

  • alkaline earth metals

    Members of group 2A in the periodic table. (Section 7.7)

  • alkyl group

    A group that is formed by removing a hydrogen atom from an alkane. (Section 25.3)

  • alkynes

    Hydrocarbons containing one or more carbon–carbon triple bonds. (Section 24.2)

  • b-Pleated sheet

    A type of polypeptide secondary structure in which sections of polypeptide chains are aligned parallel or antiparallel to one another.

  • Chain-growth polymerization

    A polymerization that involves sequential addition reactions, either to unsaturated monomers or to monomers possessing other reactive functional groups.

  • dehydrohalogenation

    An elimination reaction involving the loss of H and a halogen (such as Cl, Br, or I).

  • downfield

    The left side of an NMR spectrum.

  • electronic structure

    The arrangement of electrons in an atom or molecule. (Chapter 6:Introduction)

  • frontier orbital theory

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

  • Haworth projection

    A way to view furanose and pyranose forms of monosaccharides. The ring is drawn fl at and most commonly viewed through its edge with the anomeric carbon on the right and the oxygen atom of the ring to the rear

  • homotopic

    Protons that are interchangeable by rotational symmetry.

  • law of mass action

    The rules by which the equilibrium constant is expressed in terms of the concentrations of reactants and products, in accordance with the balanced chemical equation for the reaction. (Section 15.2)

  • Order of precedence of functions

    A ranking of functional groups in order of priority for the purposes of IUPAC nomenclature.

  • pH

    The negative log in base 10 of the aquated hydrogen ion concentration: pH = -log3H+4. (Section 16.4)

  • product

    A substance produced in a chemical reaction; it appears to the right of the arrow in a chemical equation. (Section 3.1)

  • Rate determining step

    The step in a multistep reaction sequence that crosses the highest energy barrier.

  • Secondary (2°) amine

    An amine in which nitrogen is bonded to two carbons and one hydrogen

  • symmetry allowed

    A reaction that obeys conservation of orbital symmetry.

  • tertiary

    A term used to indicate that exactly three alkyl groups are attached directly to a particular position. For example, a tertiary carbocation has three alkyl groups attached directly to the electrophilic carbon atom (C+).

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