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Solutions for Chapter 16: Aldehydes and Ketones

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9781133952848

Organic Chemistry | 7th Edition | ISBN: 9781133952848 | Authors: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Solutions for Chapter 16: Aldehydes and Ketones

Solutions for Chapter 16
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Textbook: Organic Chemistry
Edition: 7
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
ISBN: 9781133952848

This expansive textbook survival guide covers the following chapters and their solutions. Since 73 problems in chapter 16: Aldehydes and Ketones have been answered, more than 12475 students have viewed full step-by-step solutions from this chapter. Chapter 16: Aldehydes and Ketones includes 73 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781133952848. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.

Key Chemistry Terms and definitions covered in this textbook
  • Anomers

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

  • battery.

    A galvanic cell, or a series of combined galvanic cells, that can be used as a source of direct electric current at a constant voltage. (18.6)

  • bomb calorimeter

    A device for measuring the heat evolved in the combustion of a substance under constant-volume conditions. (Section 5.5)

  • chemistry

    The scientific discipline that studies the composition, properties, and transformations of matter. (Chapter 1: Introduction)

  • closest packing.

    The most efficient arrangements for packing atoms, molecules, or ions in a crystal. (11.4)

  • Correlation tables

    Tables of data on absorption patterns of functional groups.

  • dextrorotatory, or merely dextro or d

    A term used to label a chiral molecule that rotates the plane of polarization of plane-polarized light to the right (clockwise). (Section 23.4)

  • exothermic process

    A process in which a system releases heat to its surroundings. (Section 5.2)

  • functional group

    An atom or group of atoms that imparts characteristic chemical properties to an organic compound. (Section 24.1)

  • half-reaction

    An equation for either an oxidation or a reduction that explicitly shows the electrons involved, for example, Zn2 + 1aq2 + 2 e- ¡ Zn1s2. (Section 20.2)

  • heat of vaporization

    The enthalpy change, ?H, for vaporization of a liquid. (Section 11.4)

  • Henderson-Hasselbalch equation

    An equation that is often employed to calculate the pH of buffered solutions: pH = pKa + log 3conjugated base4 3acid4

  • Lactone

    A cyclic ester.

  • Nitrile

    A compound containing a !C#N (cyano) group bonded to a carbon atom.

  • Orbital

    A region of space that can hold two electrons

  • Soap

    A sodium or potassium salt of a fatty acid

  • standard emf, also called the standard cell potential 1E°2

    The emf of a cell when all reagents are at standard conditions. (Section 20.4)

  • Tertiary structure of nucleic acids

    The threedimensional arrangement of all atoms of a nucleic acid, commonly referred to as supercoiling

  • Thermoplastic

    A polymer that can be melted and molded into a shape that is retained when it is cooled.

  • thiolate

    The conjugate base of a thiol.

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