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Solutions for Chapter 3.14SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 3.14SE

Solutions for Chapter 3.14SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Since 2 problems in chapter 3.14SE have been answered, more than 66472 students have viewed full step-by-step solutions from this chapter. Chapter 3.14SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • activated complex (transition state)

    The particular arrangement of atoms found at the top of the potential-energy barrier as a reaction proceeds from reactants to products. (Section 14.5)

  • Allyl

    A !CH2CH"CH2 group.

  • antibonding molecular orbital

    A molecular orbital in which electron density is concentrated outside the region between the two nuclei of bonded atoms. Such orbitals, designated as s* or p*, are less stable (of higher energy) than bonding molecular orbitals. (Section 9.7)

  • Aufbau principle

    A rule that determines the order in which orbitals are filled by electrons. Specifically, the lowest energy orbital is filled first.

  • Brønsted-Lowry base

    A compound that can serve as a proton acceptor.

  • carboxylic acids.

    Acids that contain the carboxyl group —COOH. (24.4)

  • common-ion effect

    A shift of an equilibrium induced by an ion common to the equilibrium. For example, added Na2SO4 decreases the solubility of the slightly soluble salt BaSO4, or added NaF decreases the percent ionization of HF. (Section 17.1)

  • diazonium salt

    An ionic compound that is formed upon treatment of a primary amine with NaNO2 and HCl.

  • Dipeptide

    A molecule containing two amino acid units joined by a peptide bond

  • intermetallic compound

    A homogeneous alloy with definite properties and a fixed composition. Intermetallic compounds are stoichiometric compounds that form between metallic elements. (Section 12.3)

  • ionic bond

    A bond between oppositely charged ions. The ions are formed from atoms by transfer of one or more electrons. (Section 8.1)

  • ionic solids

    Solids that are composed of ions. (Section 12.1)

  • Kinetic control

    Experimental conditions under which the composition of the product mixture is determined by the relative rates of formation of each product.

  • lipid

    Naturally occurring compoundsthat can be extracted from cells usingnonpolar organic solvents.

  • Meta (m)

    Refers to groups occupying 1,3-positions on a benzene ring.

  • phenolate

    The conjugate base of phenol or a substituted phenol.

  • Prochiral hydrogens

    Refers to two hydrogens bonded to a carbon atom. When a different atom replaces one or the other, the carbon becomes a chiral center. The hydrogens of the CH2 group of ethanol, for example, are prochiral. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol

  • Reactive intermediate

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

  • resonance structures

    A series of structures that are melded together (conceptually) to circumvent the inadequacies of bond-line drawings.

  • Stereoselective reaction

    A reaction in which one stereoisomer is formed in preference to all others. A stereoselective reaction may be enantioselective or diastereoselective, as the case may be.

Textbook Survival Guides

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