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Solutions for Chapter Chapter 11: EDTA Titration

Quantitative Chemical Analysis | 8th Edition | ISBN: 9781429218153 | Authors: Daniel C. Harris

Full solutions for Quantitative Chemical Analysis | 8th Edition

ISBN: 9781429218153

Quantitative Chemical Analysis | 8th Edition | ISBN: 9781429218153 | Authors: Daniel C. Harris

Solutions for Chapter Chapter 11: EDTA Titration

Solutions for Chapter Chapter 11
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Textbook: Quantitative Chemical Analysis
Edition: 8
Author: Daniel C. Harris
ISBN: 9781429218153

Since 46 problems in chapter Chapter 11: EDTA Titration have been answered, more than 40781 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Quantitative Chemical Analysis, edition: 8. Quantitative Chemical Analysis was written by and is associated to the ISBN: 9781429218153. Chapter Chapter 11: EDTA Titration includes 46 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • [4+2]-cycloaddition

    A pericyclic reaction, also called a Diels-Alder reaction, that takes place between two different p systems, one of which is associated with four atoms while the other is associated with two atoms.

  • alkaloids

    Naturally occurring amines isolated from plants.

  • bond-line structures

    The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.

  • Chain termination

    A step in a chain reaction that involves destruction of reactive intermediates

  • diol

    A compound containing two hydroxyl groups (OH).

  • disrotatory

    In electrocyclicreactions, a type of rotation in which the orbitalsbeing used to form the new s bond must rotate in opposite directions (one rotates clockwise while the other rotates counterclockwise).

  • E,Z system

    A system to specify the confi guration of groups about a carbon-carbon double bond

  • high-spin complex

    A complex whose electrons populate the d orbitals to give the maximum number of unpaired electrons. (Section 23.6)

  • Hofmann product

    The less substituted product (alkene) of an elimination reaction.

  • Hydroxyl group

    An !OH group

  • ionic bond

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

  • irreversible process

    A process that cannot be reversed to restore both the system and its surroundings to their original states. Any spontaneous process is irreversible. (Section 19.1)

  • isoelectronic series

    A series of atoms, ions, or molecules having the same number of electrons. (Section 7.3)

  • molality

    The concentration of a solution expressed as moles of solute per kilogram of solvent; abbreviated m. (Section 13.4)

  • Nonbonding electrons

    Valence electrons not involved in forming covalent bonds. Also called unshared pairs or lone pairs.

  • Optical purity

    The specifi c rotation of a mixture of enantiomers divided by the specifi c rotation of the enantiomerically pure substance (expressed as a percent). Optical purity is numerically equal to enantiomeric excess, but experimentally determined.

  • peroxides

    Compounds with the general structure R!O!O!R.

  • pi 1P2 bond

    A covalent bond in which electron density is concentrated above and below the internuclear axis. (Section 9.6)

  • positron

    A particle with the same mass as an electron but with a positive charge, 0 +1e, or b+. (Section 21.1)

  • S

    A term used to designate the configuration of a chirality center, determined in the following way: Each of the four groups is assigned a priority, and the molecule is then rotated (if necessary) so that the #4 group is directed behind the page (on a dash). A counterclockwise sequence for 1-2-3 is designated as S.

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