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Solutions for Chapter 4: Arrangement ofElectrons inAtoms

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition

ISBN: 9780547586632

Modern Chemistry: Student Edition 2012 | 1st Edition | ISBN: 9780547586632 | Authors: Jerry L. Sarquis, Mickey Sarquis

Solutions for Chapter 4: Arrangement ofElectrons inAtoms

Solutions for Chapter 4
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Textbook: Modern Chemistry: Student Edition 2012
Edition: 1
Author: Jerry L. Sarquis, Mickey Sarquis
ISBN: 9780547586632

Chapter 4: Arrangement ofElectrons inAtoms includes 72 full step-by-step solutions. Modern Chemistry: Student Edition 2012 was written by Patricia and is associated to the ISBN: 9780547586632. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2012, edition: 1. Since 72 problems in chapter 4: Arrangement ofElectrons inAtoms have been answered, more than 14148 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • bimolecular reaction

    An elementary reaction that involves two molecules. (Section 14.6)

  • Carboxylic ester

    A derivative of a carboxylic acid in which H of the carboxyl group is replaced by a carbon.

  • chemical changes

    Processes in which one or more substances are converted into other substances; also called chemical reactions. (Section 1.3)

  • chemical equilibrium

    A state of dynamic balance in which the rate of formation of the products of a reaction from the reactants equals the rate of formation of the reactants from the products; at equilibrium the concentrations of the reactants and products remain constant. (Section 4.1;Chapter 15: Introduction)

  • Clemmensen reduction

    A reaction in which a carbonyl group is completely reduced and replaced with two hydrogen atoms.

  • Constitutional isomers

    Compounds with the same molecular formula but a different connectivity of their atoms

  • disulfide

    A compound with the structure R!S!S!R.

  • d–d transition

    The transition of an electron in a transition-metal compound from a lower-energy d orbital to a higher-energy d orbital. (Section 23.6)

  • electron domain

    In the VSEPR model, a region about a central atom in which an electron pair is concentrated. (Section 9.2)

  • force

    A push or a pull. (Section 5.1)

  • hemiacetal

    A compound containing a hydroxyl group (OH) and an alkoxy group (OR) connected to the same carbon atom.

  • Homotopic groups

    Atoms or groups on an atom that give an achiral molecule when one of the groups is replaced by another group. The hydrogens of the CH2 group of propane, for example, are homotopic. Replacing either one of them with deuterium gives 2-deuteropropane, which is achiral. Homotopic groups have identical chemical shifts under all conditions

  • Lewis base

    An electron-pair donor. (Section 16.11)

  • Michael acceptor

    The electrophile in a Michael reaction.

  • miscible

    Two liquids that can be mixed with each other in any proportion.

  • monodentate ligand

    A ligand that binds to the metal ion via a single donor atom. It occupies one position in the coordination sphere. (Section 23.3)

  • saturated hydrocarbon

    A hydrocarbon that contains no p bonds.

  • solvation

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

  • Sulfi de

    The sulfur analog of an ether; a molecule containing a sulfur atom bonded to two carbon atoms. Sulfi des are also called thioethers

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.

Textbook Survival Guides

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