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Solutions for Chapter 16: ACID-BASE EQUILIBRIA

Chemistry: The Central Science | 11th Edition | ISBN: 9780136006176 | Authors: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward

Full solutions for Chemistry: The Central Science | 11th Edition

ISBN: 9780136006176

Chemistry: The Central Science | 11th Edition | ISBN: 9780136006176 | Authors: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward

Solutions for Chapter 16: ACID-BASE EQUILIBRIA

Solutions for Chapter 16
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Textbook: Chemistry: The Central Science
Edition: 11
Author: Theodore E. Brown, H. Eugene H LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward
ISBN: 9780136006176

Chapter 16: ACID-BASE EQUILIBRIA includes 117 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science , edition: 11. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by Patricia and is associated to the ISBN: 9780136006176. Since 117 problems in chapter 16: ACID-BASE EQUILIBRIA have been answered, more than 4654 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Anomers

    Carbohydrates that differ in confi guration only at their anomeric carbons.

  • binary compounds.

    Compounds formed from just two elements. (2.7)

  • Brønsted base.

    A substance capable of accepting a proton. (4.3)

  • catalyst

    A substance that changes the speed of a chemical reaction without itself undergoing a permanent chemical change in the process. (Section 14.7)

  • complete ionic equation

    A chemical equation in which dissolved strong electrolytes (such as dissolved ionic compounds) are written as separate ions. (Section 4.2)

  • condensation polymerization

    Polymerization in which molecules are joined together through condensation reactions. (Section 12.8)

  • configuration

    The 3D spatial orientation of the groups connected to a chirality center (R or S ) or of the groups in a stereoisiomeric alkene (E or Z).

  • energy

    The capacity to do work or to transfer heat. (Section 5.1)

  • enol

    A compound containing a hydroxyl group (OH) connected directly to a carbon-carbon double bond.

  • hole

    A vacancy in the valence band of a semiconductor, created by doping. (Section 12.7)

  • Lewis dot structure

    The symbol of an element surrounded by a number of dots equal to the number of electrons in the valence shell of the atom

  • loss of a leaving group

    One of the four arrow-pushing patterns for ionic reactions.

  • Micelle

    A spherical arrangement of organic molecules in water solution clustered so that their hydrophobic parts are buried inside the sphere and their hydrophilic parts are on the surface of the sphere and in contact with water

  • primary structure

    For proteins, the sequence of amino acid residues.

  • reducing agent, or reductant

    The substance that is oxidized and thereby causes the reduction of some other substance in an oxidation–reduction reaction. (Section 20.1)

  • resolution

    The separation of enantiomers from a mixture containing both enantiomers.

  • second-order reaction

    A reaction in which the overall reaction order (the sum of the concentration- term exponents) in the rate law is 2. (Section 14.4)

  • Stork enamine synthesis

    A Michaelreaction in which an enamine functions as anucleophile.

  • Vinyl group

    A carbocation in which the positive charge is on one of the carbons of a carbon-carbon double bond.

  • Ylide

    A neutral molecule with positive and negative charges on adjacent atoms

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