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Solutions for Chapter 8: Monoprotic Acid-Base Equilibria

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 8: Monoprotic Acid-Base Equilibria

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

This expansive textbook survival guide covers the following chapters and their solutions. Since 57 problems in chapter 8: Monoprotic Acid-Base Equilibria have been answered, more than 125698 students have viewed full step-by-step solutions from this chapter. Chapter 8: Monoprotic Acid-Base Equilibria includes 57 full step-by-step solutions. Quantitative Chemical Analysis was written by and is associated to the ISBN: 9781429218153. This textbook survival guide was created for the textbook: Quantitative Chemical Analysis, edition: 8.

Key Chemistry Terms and definitions covered in this textbook
  • aliphatic hydrocarbons.

    Hydrocarbons that do not contain the benzene group or the benzene ring. (24.1)

  • alpha (a) anomer

    The cyclic hemiacetal of an aldose in which the hydroxyl group at the anomeric position is trans to the CH2OH

  • amplitude.

    The vertical distance from the middle of a wave to the peak or trough. (7.1)

  • atomic number

    The number of protons in the nucleus of an atom of an element. (Section 2.3)

  • biodegradable

    Organic material that bacteria are able to oxidize. (Section 18.4)

  • cell potential

    The potential difference between the cathode and anode in an electrochemical cell; it is measured in volts: 1 V = 1 J>C. Also called electromotive force. (Section 20.4)

  • chemical kinetics.

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (13.1)

  • Chiral center

    A tetrahedral atom, most commonly carbon, that is bonded to four different groups; also called a chirality center

  • complex ion.

    An ion containing a central metal cation bonded to one or more molecules or ions. (16.10)

  • Conformation

    Any three-dimensional arrangement of atoms in a molecule that results from rotation about a single bond.

  • cycloaddition reactions

    Reactions in which two p systems are joined together in a way that forms a ring. In the process, two p bonds are converted into two s bonds.

  • E (Section 5.2C)

    From the German, entgegen, opposite. Specifi es that groups of higher priority on the carbons of a double bond are on opposite sides

  • electrospray ionization (ESI):

    In mass spectrometry, an ionization technique in which the compound is first dissolved in a solvent and then sprayed via a high-voltage needle into a vacuum chamber. The tiny droplets of solution become charged by the needle, and subsequent evaporation forms gas-phase molecular ions that typically carry one or more charges.

  • Enantiotopic groups

    Atoms or groups on an atom that give a chiral center when one of the groups is replaced by another group. A pair of enantiomers results. The hydrogens of the CH2 group of ethanol, for example, are enantiotopic. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol. Enantiotopic groups have identical chemical shifts in achiral environments but different chemical shifts in chiral environments.

  • Gibbs free energy change (DG°)

    The energy that dictates the position of chemical equilibria and rates of chemical reactions. A thermodynamic function of enthalpy, entropy, and temperature, given by the equation DG° 5 DH° 2 TDS°. If DG° , 0, the position of equilibria for the reaction favors products. If DG° . 0, the position of equilibria favors reactants.

  • hydrocracking

    A process performed in the presence of hydrogen gas by which large alkanes in petroleum are converted into smaller alkanes that are more suitable for use as gasoline.

  • N-Terminal amino acid

    The amino acid at the end of a polypeptide chain having the free !NH2 group

  • oxymercuration-demercuration

    A two-step process for the Markovnikov addition of water across an alkene. With this process, carbocation rearrangements do not occur.

  • second order

    A reaction that has a rate equation in which the sum of all exponents is two.

  • singlet

    In NMR spectroscopy, a signal that is comprised of only one peak.