Solutions for Chapter 1.2: How the Electrons in an Atom Are Distributed

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 1.2: How the Electrons in an Atom Are Distributed

This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Chapter 1.2: How the Electrons in an Atom Are Distributed includes 3 full step-by-step solutions. Since 3 problems in chapter 1.2: How the Electrons in an Atom Are Distributed have been answered, more than 9802 students have viewed full step-by-step solutions from this chapter. Organic Chemistry was written by Patricia and is associated to the ISBN: 9780321803221.

Key Chemistry Terms and definitions covered in this textbook
  • activity series.

    A summary of the results of many possible displacement reactions. (4.4)

  • alkanamine

    A format for naming primary amines containing a complex alkyl group.

  • atomic mass unit (amu)

    A unit based on the value of exactly 12 amu for the mass of the isotope of carbon that has six protons and six neutrons in the nucleus. (Sections 2.3 and 3.3)

  • Aufbau principle.

    As protons are added one by one to the nucleus to build up the elements, electrons similarly are added to the atomic orbitals. (7.9)

  • Bonding molecular orbital

    A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals

  • crossed Claisen condensation

    A Claisen condensation reaction that occurs between different partners.

  • crown ether

    Cyclic polyethers whose molecular models resemble crowns.

  • electron-domain geometry

    The three- dimensional arrangement of the electron domains around an atom according to the VSEPR model. (Section 9.2)

  • Electrophile

    From the Greek meaning electron loving. Any species that can accept a pair of electrons to form a new covalent bond; alternatively, a Lewis acid.

  • frequency

    The number of times per second that one complete wavelength passes a given point. (Section 6.1)

  • Furanose

    A fi ve-membered cyclic form of a monosaccharide.

  • Lipid bilayer

    A back-to-back arrangement of phospholipid monolayers, often forming a closed vesicle or membrane.

  • nitrosonium ion

    The NO+ ion, which is formed when NaNO2 is treated with HCl.

  • nucleophilic aromatic substitution

    A substitution reaction in which an aromatic ring is attacked by a nucleophile, which replaces a leaving group.

  • Nucleoside

    A building block of nucleic acids, consisting of d-ribose or 2-deoxy-d-ribose bonded to a heterocyclic aromatic amine base by a b-N-glycosidic bond

  • petroleum

    A naturally occurring combustible liquid composed of hundreds of hydrocarbons and other organic compounds. (Section 5.8)

  • radioisotope

    An isotope that is radioactive; that is, it is undergoing nuclear changes with emission of radiation. (Section 21.1)

  • stereospecific

    A reaction in which the configuration of the product is dependent on the configuration of the starting material.

  • syn-coplanar

    A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of exactly 0°.

  • tetrahedral intermediate

    An intermediate with tetrahedral geometry. This type of intermediate is formed when a nucleophile attacks the carbonyl group of a carboxylic acid derivative.

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