×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide

Solutions for Chapter 14: Chemistry: A Molecular Approach 3rd Edition

Chemistry: A Molecular Approach | 3rd Edition | ISBN: 9780321809247 | Authors: Nivaldo J. Tro

Full solutions for Chemistry: A Molecular Approach | 3rd Edition

ISBN: 9780321809247

Chemistry: A Molecular Approach | 3rd Edition | ISBN: 9780321809247 | Authors: Nivaldo J. Tro

Solutions for Chapter 14

Solutions for Chapter 14
4 5 0 349 Reviews
17
3
Textbook: Chemistry: A Molecular Approach
Edition: 3
Author: Nivaldo J. Tro
ISBN: 9780321809247

Chemistry: A Molecular Approach was written by and is associated to the ISBN: 9780321809247. Chapter 14 includes 233 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: A Molecular Approach, edition: 3. This expansive textbook survival guide covers the following chapters and their solutions. Since 233 problems in chapter 14 have been answered, more than 379611 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Alditol

    The product formed when the C"O group of a monosaccharide is reduced to a CHOH group.

  • Allylic carbocation

    A carbocation in which an allylic carbon bears the positive charge.

  • critical temperature

    The highest temperature at which it is possible to convert the gaseous form of a substance to a liquid. The critical temperature increases with an increase in the magnitude of intermolecular forces. (Section 11.4)

  • downfield

    The left side of an NMR spectrum.

  • Endergonic reaction

    A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials

  • Exergonic reaction

    A reaction in which the Gibbs free energy of the products is lower than that of the reactants. The position of equilibrium for an exergonic reaction favors products.

  • folding

    The process by which a protein adopts its biologically active shape. (Section 24.7)

  • Gibbs free energy change (DG°)

    The energy that dictates the position of chemical equilibria and rates of chemical reactions. A thermodynamic function of enthalpy, entropy, and temperature, given by the equation DG° 5 DH° 2 TDS°. If DG° , 0, the position of equilibria for the reaction favors products. If DG° . 0, the position of equilibria favors reactants.

  • green chemistry

    Chemistry that promotes the design and application of chemical products and processes that are compatible with human health and that preserve the environment. (Section 18.5)

  • ignal splitting in NMR

    Spin-spin coupling with adjacent nuclei split NMR signals depending on the extent of coupling and the number of adjacent equivalent nuclei.

  • lecithins

    Phosphoglycerides thatcontain choline.

  • metallic solids

    Solids that are composed of metal atoms. (Section 12.1)

  • molecular hydrides

    Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)

  • polar reaction

    A reaction that involves the participation of ions as reactants, intermediates, or products.

  • polydentate ligand

    A ligand in which two or more donor atoms can coordinate to the same metal ion. (Section 23.3)

  • random copolymer

    A polymer, comprised of more than one kind of repeating unit, in which there is a random distribution of repeating units.

  • reaction rate

    A measure of the decrease in concentration of a reactant or the increase in concentration of a product with time. (Section 14.2)

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

  • Wolff-Kishner reduction

    A method for converting a carbonyl group into a methylene group (CH2) under basic conditions.

×
Log in to StudySoup
Get Full Access to Chemistry - Textbook Survival Guide
Join StudySoup for FREE
Get Full Access to Chemistry - Textbook Survival Guide
×
Reset your password