Solutions for Chapter 6: Organic Chemistry 6th Edition

Organic Chemistry | 6th Edition | ISBN: 9780840054982 | Authors: William H. Brown and Lawrence S. Brown

Full solutions for Organic Chemistry | 6th Edition

ISBN: 9780840054982

Organic Chemistry | 6th Edition | ISBN: 9780840054982 | Authors: William H. Brown and Lawrence S. Brown

Solutions for Chapter 6

Solutions for Chapter 6
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Textbook: Organic Chemistry
Edition: 6
Author: William H. Brown and Lawrence S. Brown
ISBN: 9780840054982

Chapter 6 includes 49 full step-by-step solutions. Organic Chemistry was written by Sieva Kozinsky and is associated to the ISBN: 9780840054982. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. This expansive textbook survival guide covers the following chapters and their solutions. Since 49 problems in chapter 6 have been answered, more than 16609 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • amphoteric oxides and hydroxides

    Oxides and hydroxides that are only slightly soluble in water but that dissolve in either acidic or basic solutions. (Section 17.5)

  • boiling point.

    The temperature at which the vapor pressure of a liquid is equal to the external atmospheric pressure. (11.8)

  • Boyle’s law

    A law stating that at constant temperature, the product of the volume and pressure of a given amount of gas is a constant. (Section 10.3)

  • dextrorotatory

    A compound that rotates plane-polarized light in a clockwise direction (+).

  • 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

  • eicosanoids

    A class of lipids which includes leukotrienes, prostaglandins, thromboxanes, and prostacyclins.

  • Elastomer

    A material that, when stretched or otherwise distorted, returns to its original shape when the distorting force is released.

  • electron affinity

    The energy change that occurs when an electron is added to a gaseous atom or ion. (Section 7.5)

  • Fischer projection

    A twodimensional representation of a molecule; in these projections, groups on the right and left are by convention in front, while those at the top and bottom are to the rear.

  • Histone

    A protein, particularly rich in the basic amino acids lysine and arginine, that is found associated with DNA molecules

  • Hückel criteria for aromaticity

    To be aromatic, a monocyclic compound must have one 2p orbital on each atom of the ring, be planar or nearly so, and have (4n 1 2) p electrons in the cyclic arrangement of 2p orbitals

  • labile

    Protons that are exchanged at a rapid rate.

  • Mutarotation

    The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.

  • Part per million (ppm)

    Units used on NMR spectra to record chemical shift relative to the TMS standard.

  • racemic mixture

    A solution containing equal amounts of both enantiomers.

  • radical inhibitor

    A compound that prevents a radical chain process from either getting started or continuing.

  • retro-aldol reaction

    The reverse of an aldol reaction. A b-hydroxyketone or aldehyde is converted into two ketones or aldehydes.

  • retrosynthetic analysis

    A systematic set of principles that enable the design of a synthetic route by working backward from the desired product.

  • s-trans

    A conformation of a conjugateddiene in which the disposition of the two p bonds with regard to the connecting single bond is translike (a dihedral angle of 180°).

  • shielded

    In NMR spectroscopy,protons or carbon atoms whose surrounding electron density is rich.

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