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Solutions for Chapter 4.3: Trends in the Periodic Table

Modern Chemistry: Student Edition 2006 | 1st Edition | ISBN: 9780030391071 | Authors: R. Thomas Myers, Keith B. Oldham, Salvatore Tocci

Full solutions for Modern Chemistry: Student Edition 2006 | 1st Edition

ISBN: 9780030391071

Modern Chemistry: Student Edition 2006 | 1st Edition | ISBN: 9780030391071 | Authors: R. Thomas Myers, Keith B. Oldham, Salvatore Tocci

Solutions for Chapter 4.3: Trends in the Periodic Table

Solutions for Chapter 4.3
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Textbook: Modern Chemistry: Student Edition 2006
Edition: 1
Author: R. Thomas Myers, Keith B. Oldham, Salvatore Tocci
ISBN: 9780030391071

Chapter 4.3: Trends in the Periodic Table includes 18 full step-by-step solutions. Modern Chemistry: Student Edition 2006 was written by Patricia and is associated to the ISBN: 9780030391071. Since 18 problems in chapter 4.3: Trends in the Periodic Table have been answered, more than 13404 students have viewed full step-by-step solutions from this chapter. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Modern Chemistry: Student Edition 2006, edition: 1.

Key Chemistry Terms and definitions covered in this textbook
  • alkoxy substituent

    An OR group.

  • auxochrome

    When applying Woodward-Fieser rules, the groups attached to the chromophore.

  • Betaine

    A neutral molecule with nonadjacent positive and negative charges. An example of a betaine is the intermediate formed by addition of a Wittig reagent to an aldehyde or ketone

  • Bonding electrons

    Valence electrons involved in forming a covalent bond (i.e., shared electrons).

  • bromonium ion

    A positively charged, bridged intermediate formed during the addition reaction that occurs when an alkene is treated with molecular bromine (Br2).

  • Carbocation

    A species in which a carbon atom has only six electrons in its valence shell and bears a positive charge

  • dipole–dipole force

    A force that becomes significant when polar molecules come in close contact with one another. The force is attractive when the positive end of one polar molecule approaches the negative end of another. (Section 11.2)

  • heterogeneous catalyst

    A catalyst that is in a different phase from that of the reactant substances. (Section 14.7)

  • Hofmann rule

    Any b-elimination that occurs preferentially to give the less substituted alkene as the major product.

  • locant

    In nomenclature, a numberused to identify the location of a substituent.

  • net ionic equation

    A chemical equation for a solution reaction in which soluble strong electrolytes are written as ions and spectator ions are omitted. (Section 4.2)

  • nitration

    An electrophilic aromatic substitution reaction that involves the installation of a nitro group (NO2) on an aromatic ring.

  • nomenclature

    A system for naming organic compounds.

  • Oil

    When used in the context of fats and oils, a mixture of triglycerides that is liquid at room temperature

  • osmotic pressure

    The pressure that must be applied to a solution to stop osmosis from pure solvent into the solution. (Section 13.5)

  • oxaphosphetane

    An intermediate that is believed to be formed during Wittig reactions.

  • oxime

    A compound with the structure R2CRN!OH.

  • phenoxide

    The conjugate base of phenol or a substituted phenol.

  • Polyurethane

    A polymer containing the !NHCO2! group as a repeating unit

  • Tertiary structure of proteins

    The three-dimensional arrangement in space of all atoms in a single polypeptide chain.

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