Solutions for Chapter 14: Organic Chemistry 2nd Edition

Organic Chemistry | 2nd Edition | ISBN: 9781118454312 | Authors: David R. Klein

Full solutions for Organic Chemistry | 2nd Edition

ISBN: 9781118454312

Organic Chemistry | 2nd Edition | ISBN: 9781118454312 | Authors: David R. Klein

Solutions for Chapter 14

Solutions for Chapter 14
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Textbook: Organic Chemistry
Edition: 2
Author: David R. Klein
ISBN: 9781118454312

Chapter 14 includes 43 full step-by-step solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 2. This expansive textbook survival guide covers the following chapters and their solutions. Organic Chemistry was written by Sieva Kozinsky and is associated to the ISBN: 9781118454312. Since 43 problems in chapter 14 have been answered, more than 43784 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • Acyl group

    An RCO! or ArCO! group.

  • Anomers

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

  • antiferromagnetism

    A form of magnetism in which unpaired electron spins on adjacent sites point in opposite directions and cancel each other’s effects. (Section 23.1)

  • chair conformation

    The lowest energy conformation for cyclohexane, in which all bond angles are fairly close to 109.5° and all hydrogen atoms are staggered.

  • decomposition reaction.

    The breakdown of a compound into two or more components. (4.4)

  • frequency

    The number of times per second that one complete wavelength passes a given point. (Section 6.1)

  • glucose

    A polyhydroxy aldehyde whose formula is CH2OH1CHOH24CHO; it is the most important of the monosaccharides. (Section 24.8)

  • Haworth projection

    For substituted cycloalkanes, a drawing style used to clearly identify which groups are above the ring and which groups are below the ring. (See also Sect. 4.14.)

  • Haworth projection

    A way to view furanose and pyranose forms of monosaccharides. The ring is drawn fl at and most commonly viewed through its edge with the anomeric carbon on the right and the oxygen atom of the ring to the rear

  • hydration

    Solvation when the solvent is water. (Section 13.1)

  • pH titration curve

    A graph of pH as a function of added titrant. (Section 17.3)

  • photochemical reaction

    A reaction that is performed with photochemical excitation (usually UV light).

  • pi 1P2 molecular orbital

    A molecular orbital that concentrates the electron density on opposite sides of an imaginary line that passes through the nuclei. (Section 9.8)

  • property

    A characteristic that gives a sample of matter its unique identity. (Section 1.1)

  • Solvolysis

    A nucleophilic substitution in which the solvent is also the nucleophile

  • tautomers

    Constitutional isomers that rapidly interconvert via the migration of a proton.

  • trigonal pyramidal

    A geometry adopted by an atom that has one lone pair and a steric number of 4.

  • Vibrational infrared region

    A common type of spin-spin coupling involving the H atoms on two C atoms that are bonded to each other.

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.

  • Williamson ether synthesis

    A general method for the synthesis of dialkyl ethers by an SN2 reaction between a haloalkane and an alkoxide ion.

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